Protein composition having isoprene polymerization activity and use thereof

Abstract

To provide means for achieving the efficient production and stable securing of natural rubber in order to stably secure rubber resources.SOLUTION: The present invention provides a protein composition having an isoprene polymerization activity, containing: (A-1) a protein with the same activity as CPT6, or (A-2) a protein with the same activity as CPT7; and (B) a protein with the same activity as CPTL, a lipid membrane construct comprising the composition, a method for manufacturing the same, cells that express the proteins that make up the composition, a method for making the same, and a method for manufacturing an isoprene polymerized compound using any of these.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a protein composition having isoprene polymerization activity and uses thereof, and more particularly, to a protein composition having isoprene polymerization activity, a lipid membrane construct and a cell containing the same, and a method for producing an isoprene polymerization compound using the same. [Background technology]

[0002] Natural rubber is a substance whose main component is cis-polyisoprene contained in the sap of rubber trees, and is widely used in various fields such as the automotive and construction industries, with demand expanding worldwide. As natural rubber is an agricultural product harvested from rubber trees, there are problems such as unstable supply and inconsistent quality, which could pose a significant management risk. For this reason, efforts are being made to develop technology to artificially produce natural rubber.

[0003] Patent Document 1 and Non-Patent Document 1 describe a method for producing polyisoprenoids, which includes a binding step in which each gene expression product of specific proteins involved in natural rubber biosynthesis (HRT1, HRTBP, and REF) is bound to rubber particles in vitro. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Patent No. 6586693 [Non-patent literature]

[0005] [Non-Patent Document 1] Yamashita S.et al.eLife 2016;5:e19022.DOI:10.7554 / eLife.19022 Summary of the Invention [Problem to be solved by the invention]

[0006] The techniques described in Patent Document 1 and Non-Patent Document 1 were insufficient for practical use because they could not produce a sufficient amount of polyisoprenoids. Furthermore, these techniques require rubber particles to be harvested from plants, and there are problems such as the complicated harvesting process of rubber particles and the difficulty of stabilizing the quality of rubber particles because they are extracted from plants.

[0007] The present invention aims to provide a means for efficiently producing natural rubber and realizing a stable supply of the rubber, thereby ensuring a stable supply of rubber resources. [Means for solving the problem]

[0008] According to the present invention, the following [1] to

[24] are provided. [1] (A-1) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 6, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 6 and having an activity similar to that of CPT6, or (A-2) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO:8, a protein comprising the amino acid sequence of SEQ ID NO:8, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO:8 and having an activity similar to that of CPT7; (B) one or more proteins selected from a protein having the amino acid sequence of SEQ ID NO: 10 and a protein having an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 10 and having an activity similar to that of CPTL; 1. A protein composition having isoprene polymerization activity comprising: [2] (A-1) a protein encoded by one or more polynucleotides (a-1) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5 and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO:5, the polynucleotide encoding a protein having activity similar to that of CPT6; (A-2) A protein encoded by one or more polynucleotides (a-2) selected from a polynucleotide comprising the base sequence of SEQ ID NO: 7 and a polynucleotide comprising a base sequence having 90% or more identity with the base sequence of SEQ ID NO: 7, the polynucleotide encoding a protein having an activity similar to that of CPT7; and (B) The protein is encoded by one or more polynucleotides (b) selected from a polynucleotide containing the base sequence of SEQ ID NO:9 and a polynucleotide containing a base sequence having 90% or more identity to the base sequence of SEQ ID NO:9, which encodes a protein having activity similar to that of CPTL. The composition according to [1], which is at least one of the above. [3] The composition according to [1] or [2], further comprising a CPT family protein other than CPT6, 7 and CPTL, a REF family protein, and a SRPP family protein. [4] (C) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 2 and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 2 and having an activity similar to that of CPT1; (D) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 4 and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 4 and having an activity similar to that of CPT2; (E) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 12, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 12 and having an activity similar to that of REF1; (F) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 14 and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 14 and having an activity similar to that of REF2; (G) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 16, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 16 and having an activity similar to that of REF8; and (H) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 18, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 18 and having an activity similar to that of SRPP1; The composition according to [1], further comprising at least one selected from the following: [5] (C) a protein encoded by one or more polynucleotides (c) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:1 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:1, the polynucleotide encoding a protein having activity similar to that of CPT1; (D) a protein encoded by one or more polynucleotides (d) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 3, the polynucleotide encoding a protein having activity similar to that of CPT2; (E) a protein encoded by one or more polynucleotides (e) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:11 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:11, the polynucleotide encoding a protein having activity similar to that of REF1; (F) a protein encoded by one or more polynucleotides (f) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 13, the polynucleotide encoding a protein having activity similar to that of REF2; (G) A protein encoded by one or more polynucleotides (g) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 15 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 15, and encoding a protein having activity similar to that of REF8; and (H) a protein encoded by one or more polynucleotides (h) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 17, the polynucleotide encoding a protein having activity similar to that of SRPP1; The composition according to [4], which is at least one of the above. [6] The composition according to any one of [1] to [5], wherein at least one of the proteins (A) to (H) is derived from a rubber tree. [7] A lipid membrane construct comprising the composition according to any one of [1] to [6] and a phospholipid. [8] The construct according to [7], which is a lipid bilayer construct. [9] The construct according to [7] or [8], which is a proteoliposome.

[10] A method for producing the lipid membrane construct according to any one of [7] to [9], comprising expressing a polynucleotide encoding a protein constituting the composition according to any one of [1] to [6] in a cell-free protein production system in the presence of a raw material containing a phospholipid.

[11] A polynucleotide encoding a protein constituting the composition according to any one of [1] to [6], (a-1) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5 and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO:5, which encodes a protein having an activity similar to that of CPT6; or (a-2) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 7 and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO: 7, which encodes a protein having an activity similar to that of CPT7; (b) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 9 and a polynucleotide encoding a protein having an activity similar to that of CPTL, the polynucleotide comprising a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 9; A method for producing the lipid membrane construct according to

[10] , comprising:

[12] The polynucleotide is a polynucleotide encoding a protein constituting the composition according to [3] or [4]; (c) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 1 and a polynucleotide encoding a protein having activity similar to that of CPT1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 1. (d) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide encoding a protein having activity similar to that of CPT2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 3. (e) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 11, and a polynucleotide encoding a protein having an activity similar to that of REF1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 11. (f) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13 and a polynucleotide encoding a protein having an activity similar to that of REF2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 13. (g) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 15 and a polynucleotide encoding a protein having an activity similar to that of REF8, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 15; and (h) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17 and a polynucleotide encoding a protein having activity similar to that of SRPP1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 17. The method for producing a lipid membrane construct according to

[10] or

[11] , further comprising at least one of the following steps:

[13] The method for producing a lipid membrane construct according to any one of

[10] to

[12] , wherein the raw material containing a phospholipid contains a liposome, and the lipid membrane construct is a proteoliposome.

[14] A cell expressing a protein constituting the composition according to any one of [1] to [5].

[15] The cell according to

[14] , comprising an expression unit containing a polynucleotide encoding each of the proteins contained in the protein composition according to any one of [1] to [6].

[16] The polynucleotide comprises: (a-1) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5 and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO:5, which encodes a protein having an activity similar to that of CPT6; or (a-2) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 7 and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO: 7, which encodes a protein having an activity similar to that of CPT7; (b) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 9 and a polynucleotide encoding a protein having an activity similar to that of CPTL, the polynucleotide comprising a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 9; The cell according to

[14] or

[15] ,

[17] The polynucleotide is a polynucleotide encoding a protein constituting the composition according to [3] or [4]; (c) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 1 and a polynucleotide encoding a protein having activity similar to that of CPT1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 1. (d) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide encoding a protein having activity similar to that of CPT2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 3. (e) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 11, and a polynucleotide encoding a protein having an activity similar to that of REF1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 11. (f) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13 and a polynucleotide encoding a protein having an activity similar to that of REF2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 13. (g) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 15 and a polynucleotide encoding a protein having an activity similar to that of REF8, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 15; and (h) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17 and a polynucleotide encoding a protein having activity similar to that of SRPP1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 17. The cell according to any one of

[14] to

[16] , further comprising at least one of the following:

[18] The cell described in any one of

[14] to

[17] , wherein the expression unit is a heterologous expression unit.

[19] The cell described in

[14] , which comprises the lipid membrane construct described in [9].

[20] A method for producing the cell described in

[14] , comprising interacting the lipid membrane construct described in [9] with the cell.

[21] A method for producing an isoprene polymerization compound, comprising carrying out an isoprene polymerization reaction using at least one selected from the composition according to any one of [1] to [6], the construct according to [7] to [9], and the cell according to any one of

[14] to

[19] .

[22] The method according to

[21] , wherein an isoprene polymerization reaction is carried out using a low-molecular-weight allyl compound as a substrate.

[23] At least one selected from the composition according to any one of [1] to [6], the construct according to [7] to [9], and the cell according to any one of

[14] to

[19] , and Low molecular weight allyl compounds A kit for producing an isoprene polymerized compound, comprising:

[24] A method for producing rubber, comprising producing rubber using an isoprene polymer compound produced by the production method according to

[21] or

[22] . Effect of the Invention

[0009] According to the present invention, natural rubber can be efficiently produced and a stable supply can be achieved, which is expected to lead to a stable supply of rubber resources, the demand for which is expanding worldwide. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0010] [Protein Composition] (Isoprene polymerization activity) The protein composition of the present invention has isoprene polymerization activity. The isoprene polymerization activity generally means the activity of directly or indirectly promoting the polymerization reaction of isoprene to produce an isoprene polymerized compound. The polymerization reaction of isoprene is generally the polymerization reaction of isoprene in an organism. Examples of the substrate include low molecular weight allyl compounds such as isopentenyl diphosphate (IPP), farnesyl diphosphate (FPP), dimethylallyl diphosphate (DMAPP), geranyl diphosphate (GPP), and geranylgeranyl diphosphate (GGPP). Examples of living organisms include rubber trees (plants capable of producing natural rubber) such as plants of the genus Hevea (e.g., Hevea brasiliensis, Hevea benthamiana, Hevea guianensis) and plants of the genus Ficus (e.g., Ficus elastica, Ficus lyrata, Ficus benjamina), but are not limited to these, and also include other plant cells, animal cells, and microorganisms.

[0011] (Proteins Constituting the Protein Composition) (Proteins (A) and (B)) The protein composition comprises at least one of proteins (A-1) and (A-2) and a protein (B): (A-1) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 6, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 6 and having an activity similar to that of CPT6; (A-2) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 8, a protein comprising the amino acid sequence of SEQ ID NO: 8, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 8 and having an activity similar to that of CPT7; and (B) One or more proteins selected from a protein having the amino acid sequence of SEQ ID NO: 10 and a protein having an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 10 and having activity similar to CPTL.

[0012] The amino acid sequences of SEQ ID NOs: 6, 8, and 10 are the amino acid sequences of cis-prenyltransferase (CPT) 6, CPT7, and CPTL, respectively, derived from Hevea brasiliensis.

[0013] The proteins (A-1), (A-2) and (B) may be proteins encoded by polynucleotides (a-1), (a-2) and (b), respectively: (a-1) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5, and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:5, which encodes a protein having activity similar to that of CPT6; (a-2) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 7 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 7, which encodes a protein having an activity similar to that of CPT7; and (b) one or more polynucleotides selected from a polynucleotide comprising the base sequence of SEQ ID NO:9, and a polynucleotide encoding a protein having activity similar to that of CPTL, the polynucleotide comprising a polynucleotide having 90% or more identity to the base sequence of SEQ ID NO:9.

[0014] The nucleotide sequences represented by SEQ ID NOs: 5, 7 and 9 are the full-length nucleotide sequences of CPT6, CPT7 and CPTL, respectively, derived from Hevea brasiliensis.

[0015] (other proteins) The protein composition may contain proteins other than the proteins (A-1), (A-2) and (B). Examples of other proteins include proteins that are responsible for the polymerization reaction of isoprene in vivo itself and proteins that are known to assist the polymerization reaction. Examples of the former include CPT family members other than CPT6, CPT7 and CPTL. Examples of the latter include at least one selected from the rubber elongation factor (REF) family and the small rubber particle protein (SRPP) family. Among these, at least one selected from the proteins (C) to (H) is preferred: (C) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 2, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 2 and having an activity similar to that of CPT1; (D) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 4 and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 4 and having an activity similar to that of CPT2; (E) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 12, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 12 and having an activity similar to that of REF1; (F) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 14 and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 14 and having an activity similar to that of REF2; (G) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 16 and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 16 and having an activity similar to that of REF8; and (H) One or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 18, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 18 and having activity similar to SRPP1. The amino acid sequences of SEQ ID NOs: 2, 4, 12, 14, 16, and 18 comprise the mature proteins of CPT1, CPT2, REF1, REF2, REF8, and SRPP1, respectively, derived from Hevea brasiliensis.

[0016] The proteins (C) to (H) may be proteins encoded by polynucleotides (c) to (h), respectively: (c) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 1, and a polynucleotide encoding a protein having activity similar to that of CPT1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 1; (d) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide encoding a protein having an activity similar to that of CPT2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 3; (e) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 11, and a polynucleotide encoding a protein having an activity similar to that of REF1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 11; (f) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13 and a polynucleotide encoding a protein having an activity similar to that of REF2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 13; (g) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 15 and a polynucleotide encoding a protein having an activity similar to that of REF8, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 15; and (h) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17, and a polynucleotide encoding a protein having activity similar to that of SRPP1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 17.

[0017] The nucleotide sequences represented by SEQ ID NOs: 1, 3, 11, 13, 15 and 17 are the full-length nucleotide sequences of CPT1, CPT2, REF1, REF2, REF8 and SRPP1, respectively, derived from Hevea brasiliensis. The protein composition preferably contains two or more, three or more, four or more, or five or more of the proteins (C) to (H), more preferably contains a combination of at least one of (C) and (D) and at least one of (E) to (H), and even more preferably contains all of them.

[0018] (%identity) The identity of the amino acid sequence and the nucleotide sequence may be 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more. The identity can be determined, for example, using BLAST of NCBI (see http: / / www.ncbi.nlm.nih.gov) under default conditions.

[0019] (Activity of mutant proteins) "Having similar activity" to each protein means, when measured under the same conditions, having, for example, 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, 95% or more, or 100% or more of the activity of each protein.

[0020] (mutation) The above proteins may have mutations at sites in the catalytic domain and at sites outside the catalytic domain, so long as they can retain the same activity. The positions of amino acid residues in the protein where mutations may be introduced and which can retain the desired activity can be identified by those skilled in the art. For example, those skilled in the art can 1) compare the amino acid sequences of multiple proteins having the same activity (e.g., the amino acid sequences represented by SEQ ID NO: 6 or 8 and the amino acid sequences of other proteins involved in isoprene polymerization reactions), 2) clarify regions that are relatively conserved or not, and then 3) predict regions that may play an important role in function and regions that may not play an important role from the relatively conserved and non-conserved regions, thereby recognizing the correlation between structure and function and identifying the sites where mutations may be introduced.

[0021] The mutation introduced into the protein may be a substitution of an amino acid residue with another amino acid residue, and is preferably a substitution with an amino acid residue having a similar side chain. Classification of amino acids according to amino acid residues having similar side chains includes, for example, amino acids having basic side chains such as lysine, arginine, histidine, etc.; amino acids having acidic side chains such as aspartic acid, glutamic acid, etc.; amino acids having uncharged polar side chains such as asparagine, glutamine, serine, threonine, tyrosine, cysteine, etc.; amino acids having non-polar side chains such as glycine, alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan, etc.; amino acids having β-branched side chains such as threonine, valine, isoleucine, etc.; amino acids having aromatic side chains such as tyrosine, phenylalanine, tryptophan, histidine, etc.; amino acids having hydroxyl group-containing side chains (e.g., alcohol, phenoxy group-containing side chains) such as serine, threonine, tyrosine, etc.; and amino acids having sulfur-containing side chains such as cysteine, methionine, etc.

[0022] The base sequence may be modified for the purpose of codon optimization. As used herein, codon optimization means that the base sequence is modified so as to optimize expression in a specific target cell without changing the sequence of the encoded polypeptide. The optimized base sequence can be easily determined by a person skilled in the art by understanding the codon usage frequency in the cell to be introduced and utilizing the degeneracy of the genetic code. Examples of target cells include microorganisms such as E. coli, plant cells, and animal cells.

[0023] (Protein Modification) Each protein constituting the protein composition may have a purification tag near the C-terminus. Examples of purification tags include histidine tags, HA, FLAG, V5, and myc epitopes, chitin binding protein (CBP), maltose binding protein (MBP), glutathione-S-transferase (GST), and Strep tags. In addition to the above, the protein composition may contain a factor that is directly or indirectly involved in the polymerization reaction of isoprene.

[0024] [Lipid membrane construct] The lipid membrane construct of the present invention is a construct comprising a lipid membrane containing the above-mentioned protein composition. By using the lipid membrane construct, the protein composition is more likely to exhibit isoprene polymerization activity, and efficient isoprene polymerization can be achieved.

[0025] The lipid membrane may be a single membrane or a double membrane. An example of a single membrane construct is rubber particles (particles extracted from latex derived from rubber trees). An example of a double membrane construct is proteoliposomes and artificial lipid membrane models. The artificial lipid membrane model may be composed of natural lipids, synthetic lipids, or both, and is not particularly limited. The lipid membrane construct is preferably a double membrane construct, and more preferably a proteoliposome.

[0026] (Proteoliposomes) As used herein, proteoliposome refers to an artificial vesicle in which a protein is encapsulated or bound to a part of the lipid bilayer membrane of the liposome. As used herein, liposome refers to an artificial vesicle in which an aqueous component (usually water) is captured in a space formed by being surrounded by a lipid bilayer membrane. The lipid bilayer membrane is usually composed of lipids such as phospholipids. Examples of phospholipids include phosphatidylethanolamine, phosphatidylcholine, phosphatidylserine, cardiolipin, or combinations thereof. Examples of lipids other than phospholipids include triacylglycerol, wax, sphingolipids, and sterols and their fatty acid esters, or combinations thereof. The lipids constituting the lipid bilayer membrane preferably include phospholipids derived from living organisms, and more preferably include soybean-derived phospholipids.

[0027] The size of the liposome is not particularly limited, but the diameter is usually 50 to 300 nm. The liposome may be of natural origin or synthetic origin, but the former is preferable, and those derived from plants such as soybean are more preferable. As the synthetic liposome, for example, polyalkylene glycol-based liposomes can be mentioned.

[0028] The form in which the protein composition is present in the membrane lipid construct is not particularly limited, but in the case of liposomes, it is presumed that the protein composition is bound to the hydrophilic group of the phospholipid on the liposome surface (a part of the protein composition may be embedded inside the membrane).

[0029] (Manufacturing method) Examples of methods for producing membrane lipid constructs include methods comprising expressing a polynucleotide encoding a protein constituting the composition in a cell-free protein production system in the presence of a raw material containing a phospholipid.

[0030] When the membrane construct is a proteoliposome, the raw material containing phospholipids contains a liposome. As described above, the liposome is preferably a liposome of natural origin, and more preferably a liposome derived from a plant such as soybean.

[0031] The method for producing a proteoliposome preferably comprises expressing an expression unit containing the polynucleotide in a cell-free protein production system in the presence of a liposome.

[0032] The expression unit includes at least a polynucleotide encoding each protein contained in the protein composition. The polynucleotide is a polynucleotide encoding a protein constituting the protein composition, and includes the above-mentioned (a-1) or (a-2) and (b), and further includes at least one of (c) to (h) as necessary. The expression unit usually includes a promoter. This allows efficient production of an expression product of a polynucleotide encoded by the polynucleotide. Examples of the promoter include a tac promoter, a lac promoter, a trp promoter, a trc promoter, a T7 promoter, a T5 promoter, a T3 promoter, and an SP6 promoter, and may include an enhancer. The promoter may be linked to the polynucleotide in a form that allows its expression, for example, linked to the upstream (5') side of the coding sequence. The expression unit may be DNA or RNA, but is preferably DNA. The expression unit may include factors such as a terminator, a ribosome binding site, a drug resistance gene, an RNA processing signal, a sequence that improves translation efficiency, a sequence that enhances protein stability, and a sequence that enhances protein secretion.

[0033] The cell-free protein production system is preferably carried out by the dialysis overlay method using a cell extract (e.g., wheat germ extract, Escherichia coli extract, rabbit reticulocyte extract, insect cell extract), and can be carried out according to a commercially available cell-free protein expression kit.

[0034] In addition, other protein construction systems, such as artificial lipid membrane models, may be used instead of liposomes. The construction of protein composition in the artificial lipid membrane model may be performed according to a conventional method. In addition, the artificial lipid membrane model may be composed of natural lipid, synthetic lipid, or both, and is not particularly limited.

[0035] (cell) The cell of the present invention is a cell that expresses each protein constituting the protein composition (proteins (A) and (B), and, if necessary, at least one of proteins (C) to (H)). Examples of the cell include, but are not limited to, microbial cells such as Escherichia coli and yeast, plant cells, and animal cells.

[0036] The cell preferably contains an expression unit containing the polynucleotide. The expression unit is the same as that described in the description of the proteoliposome. The expression unit that the cell may contain is preferably a heterologous expression unit. As used herein, a heterologous expression unit means an expression unit in which at least one of the polynucleotides encoding each protein and the promoter normally contained therein is not endogenous to the host cell. Preferably, both are not endogenous to the host cell.

[0037] A method for producing cells includes, for example, a method of transformation with an expression vector containing an expression unit containing a polynucleotide encoding each of the proteins constituting the protein composition. Since the protein composition contains at least two proteins as described above, the expression vector may be one (containing an expression unit containing a polynucleotide encoding all of the proteins) or two or more (containing an expression unit containing each or some of the polynucleotides). The expression vector may be an integrative vector or a non-integrative vector. In the expression vector, the polynucleotide may be placed under the control of a constitutive promoter or an inducible promoter.

[0038] Transformation of a host with an expression vector can be carried out using one or more known methods. Examples of such methods include the calcium phosphate method, the liposome method, the DEAE-dextran method, the electroporation method, and particle gun (gene gun). In addition to a plasmid vector, a phage vector may be used to infect and introduce the vector into a bacterial cell.

[0039] The cell may be a cell containing the above-mentioned proteoliposome. The proteoliposome is preferably made from a liposome of natural origin. This allows easy interaction with the cell membrane. The cell containing the proteoliposome can be produced by allowing the two to interact with each other. Examples of methods for allowing the two to interact include a method of adsorbing or binding the liposome to the cell surface, a method of taking up the liposome into the cell (endocytosis or phagocytosis), and a method of fusing the lipid bilayer membrane of the liposome with the cell membrane.

[0040] [Method for producing isoprene polymer compound] The above protein compositions, proteoliposomes, and cells can be used to produce isoprene polymerized compounds.

[0041] In the production of an isoprene polymer compound, an isoprene polymerization reaction is carried out using a low molecular weight allylic compound as a substrate. Examples of low molecular weight allylic compounds include isoprenyl diphosphate and farnesyl diphosphate, and both of these are preferable. Conditions such as reaction temperature and reaction time can be set appropriately. A representative isoprene polymer compound is cis-polyisoprene, which is useful as a raw material for rubber. Other examples of isoprene polymer compounds include dolichol, polyprenol, and derivatives thereof, which exhibit physiological activities in the living body (e.g., immune activity, antiviral activity, antioxidant activity), and are therefore useful as materials for medicines and health foods. They can also be used as additives for rubber products (e.g., plasticizers, compatibilizers).

[0042] [Kit for producing isoprene polymer compound] The above protein composition, proteoliposome, and cell can be used as a kit for producing an isoprene polymerized compound. The kit usually contains a low molecular weight allyl compound as a substrate. The kit may further contain a reaction vessel and necessary reagents.

[0043] [Method of manufacturing rubber] The isoprene polymerized compound obtained by the above-mentioned method for producing an isoprene polymerized compound can be used for producing rubber. The procedure and conditions for producing rubber from an isoprene polymerized compound may be in accordance with a conventional method, for example, a method in which the isoprene polymerized compound is kneaded, crosslinked, and molded. Examples of additives that can be used as needed include reinforcing agents, silane coupling agents, fillers, vulcanizing agents, vulcanization accelerators, vulcanization accelerator assistants, oils, cured resins, waxes, antioxidants, and colorants. These additives may be added at the appropriate stage. The rubber obtained can be used for various applications such as tires, building materials, sporting goods, and automobile parts. EXAMPLES

[0044] Examples 1 to 11 (1) Isolation of natural rubber biosynthetic protein genes Seven proteins (CPT1, CPT2, CPTL, REF1, REF2, REF8, and SRPP1) that are highly produced in latex were selected from the Rubber Database (http: / / Matsui-lab.riken.jp / rubber / home.html). In addition, two proteins (CPT6 and CPT7) were selected from phylogenetic analysis.

[0045] The CPT1, CPT2, CPT6, CPT7, CPTL, REF1, REF2, REF8, and SRPP1 genes were obtained by PCR using cDNA of the gene encoding each protein or a plasmid containing each gene as a template. PCR was performed according to the instructions for PrimeSTAR Max DNA Polymerase (Takara) or KOD One PCR Master Mix (TOYOBO), and restriction enzyme digestion sites and His tag sequences were added to the primers as necessary.

[0046] The primer sets used to obtain the CPT1, CPT2, CPT6, CPT7, CPTL, REF1, REF2, REF8, and SRPP1 genes, respectively, were primers 1 and 2, primers 3 and 4, primers 5 and 6, primers 7 and 8, primers 9 and 10, primers 11 and 12, primers 13 and 14, primers 15 and 16, and primers 17 and 18.

[0047] (Primer set for obtaining CPT1 gene) Primer 1: 5'-atggaattatacaacggtg-3' (SEQ ID NO: 19) Primer 2: 5'-atctcgagttaatgatgatgatgatgatgttttaag-3' (SEQ ID NO: 20)

[0048] (Primer set for obtaining CPT2 gene) Primer 3: 5'-atggaaatatatacgggtcag-3' (SEQ ID NO: 21) Primer 4: 5'-atctcgagttaatgatgatgatgatgatgttttaaatattc-3' (SEQ ID NO: 22)

[0049] (Primer set for obtaining CPT6 gene) Primer 5: 5'-atggaaaaacatagcagtag-3' (SEQ ID NO: 23) Primer 6: 5'-atctcgagttatataactgatgctttttc-3' (SEQ ID NO: 24)

[0050] (Primer set for obtaining CPT7 gene) Primer 7: 5'-atgcaatccttgcacttg-3' (SEQ ID NO: 25) Primer 8: 5'-atctcgagttatgtaagtcgtctaccatag-3' (SEQ ID NO: 26)

[0051] (Primer set for obtaining CPTL gene) Primer 9: 5'-atggatttgaaacctgg-3' (SEQ ID NO: 27) Primer 10: 5'-atctcgagttaatgatgatgatgatgatgtgtac-3' (SEQ ID NO: 28)

[0052] (Primer set for obtaining REF1 gene) Primer 11: 5'-atggctgaaggtgaagaagaggtgaatatc-3' (SEQ ID NO: 29) Primer 12: 5'-atctcgagtcacccatctccatatagcac-3' (SEQ ID NO: 30)

[0053] (Primer set for obtaining REF2 gene) Primer 13: 5'-atggctgaagacgaagacaaccaacaag-3' (SEQ ID NO: 31) Primer 14: 5'-atctcgagtcaattctctccataaaacac-3' (SEQ ID NO: 32)

[0054] (Primer set for obtaining REF8 gene) Primer 15: 5'-atggctgaagggaaagaaaacgagaatttc-3' (SEQ ID NO: 33) Primer 16: 5'-atctcgagttactctgcactttccttcac-3' (SEQ ID NO: 34)

[0055] (Primer set for obtaining SRPP1 gene) Primer 17: 5'-atggctgaagaggtggaggaagagaggc-3' (SEQ ID NO: 35) Primer 18: 5'-atctcgagttatgatgcctcatctccaaac-3' (SEQ ID NO: 36)

[0056] The sequences of the genes obtained by the above-mentioned method were identified, and the full-length base sequences and amino acid sequences were identified. The base sequences of the CPT1, CPT2, CPT6, CPT7, CPTL, REF1, REF2, REF8, and SRPP1 genes are shown in SEQ ID NOs: 1, 3, 5, 7, 9, 11, 13, 15, and 17, respectively, and the amino acid sequences are shown in SEQ ID NOs: 2, 4, 6, 8, 10, 12, 14, 16, and 18, respectively.

[0057] (2) Preparation of plasmids for cell-free protein synthesis The PCR reaction products of each gene obtained in (1) above were treated with the restriction enzyme XhoI attached to the primer, and each combination in Table 1 was selected and inserted into the cell-free expression vector pEU-E01-MCS that had been treated with the restriction enzymes EcoRV and XhoI to prepare a plasmid for cell-free protein synthesis.

[0058] (3) Transformation of E. coli The plasmid prepared above was transformed into Escherichia coli JM109, and the transformants were cultured on LB agar medium containing ampicillin, and transformants into which the target plasmid had been introduced were selected by colony PCR.

[0059] (4) Preparation of plasmids for cell-free protein synthesis E. coli transformed with a plasmid containing the target gene was cultured overnight at 37°C on LB liquid medium, after which the cells were harvested and the plasmid was recovered. The plasmid was recovered using the FastGene Plasmid Mini Kit (Nihon Genetics). Sequence analysis was used to confirm that there were no mutations in the base sequence of the gene inserted into the recovered plasmid.

[0060] (5) Transformation of E. coli The plasmid prepared above was used to transform E. coli JM109, and the transformant was cultured on LB agar medium containing ampicillin.

[0061] (6) Recovery of plasmid for cell-free protein synthesis E. coli transformed with a plasmid containing the target gene was cultured overnight at 37°C on LB liquid medium, and then the cells were harvested and the plasmid was recovered. The plasmid was recovered using the QIAGEN Plasmid Midi Kit (QIAGEN) and adjusted to 1 μg / μl.

[0062] (7) Synthesis of membrane proteins (proteoliposomes) in the presence of liposomes by dialysis overlay method A lipid bilayer membrane (liposome: diameter of about several hundred nm) was prepared using soybean-derived phospholipids. Cell-free protein synthesis was performed under liposome addition conditions according to the protocol attached to the ProteoLiposome BD Expression Kit (Cell Free Sciences). Expression plasmids for nine types of template proteins were adjusted to 1 μg / μl and used in the combinations shown in Table 1, and were used in an equal volume ratio so that the total amount was about 13 μl. For example, in Example 3, 1.5 μL of each of the nine types was added to the transcription reaction system so that the total amount was 13.5 μL. After the synthesis reaction was completed, simple purification of Proteoliposomes in which nine types of proteins were bound to liposomes was performed according to the attached protocol, and synthesis was confirmed by SDS-PAGE.

[0063] (8) Measurement of isoprene polymerization activity The isoprene polymerization activity of the cell-free synthesized protein was measured by the following method. Final concentration 50mM Tris-HCl (pH 7.5), final concentration 10mM MgCl2, final concentration 2mM DTT, final concentration 10μM farnesyl diphosphate (FPP), 50μM final concentration 14 C-Isopentenyl diphosphate ( 14C-IPP) (specific activity: 1.48-2.22 GBq / mmol) and 5 μL proteoliposome were mixed to prepare 100 μL of reaction solution, which was then reacted at 30° C. for 24 hours.

[0064] After the reaction, 200 μL of saturated saline was added, and the reaction product was extracted with 300 μL of water-saturated n-butanol. 400 μL of 2M NaCl was added to the collected water-saturated n-butanol layer, and after suspension, the water-saturated n-butanol layer was collected. 5 mL of Clearsol II (Nacalai Tesque) was added to 50 μL of the collected solution, and after thorough mixing, the radiation dose (dpm) was measured using a liquid scintillation counter (LSC-8000; Aloka). A reaction system without the addition of proteoliposome was used as a negative control, and the results when proteoliposomes containing various proteins were used are shown in Table 1.

[0065] (9) TLC radiogram of isoprene polymerization reaction products The organic layer of the water-saturated n-butanol solution collected above was evaporated using a centrifugal evaporator. 1.5 mL of a reaction solution containing 100 mM sodium acetate (pH 5.5), 1 U acid phosphatase (from potato) and 1 mL of methanol was added and reacted at 37°C for 17 hours.

[0066] After the reaction, the mixture was extracted with 500 μL of hexane, and the resulting hexane layer was concentrated and dried using a centrifugal evaporator. The dried product was redissolved in 10 μL of hexane, and the entire amount was spotted on a TLC plate (Merck, TLC glass plate RP-18F254S 5 × 10 cm). The mixture was developed with acetone:water = 19:1, exposed to an imaging plate, and visualized using a scanner (Typhoon FLA9500).

[0067] Comparative Example 1 (negative control) The same procedure as in the above Example was carried out except that proteoliposomes were not added.

[0068] Comparative Examples 2 to 9 (other than negative control) The plasmid for cell-free synthesis of each protein was adjusted to 1 μg / μl. The total amount of plasmid in the reaction was 13.5 μl, and the amount of each plasmid was added in an equal ratio. Thereafter, the same operations as in the above examples were performed.

[0069] [Table 1]

[0070] As is clear from Table 1, the radiation dose in each Example was higher than that in the Comparative Example, and it was found that a product (estimated to have a molecular weight of about 1,000 to 2,000) was synthesized. Example 1, which is a combination of CPT6 and CPTL, and Example 2, which is a combination of CPT7 and CPTL, had a higher radiation dose than the Comparative Example, making it clear that each combination exhibits isoprene polymerization activity. Furthermore, Examples 3 to 11, which further combine other proteins, also had a higher radiation dose than the Comparative Example, and some of them had a higher radiation dose than Examples 1 and 2, making it clear that proteins other than CPT6, 7, and CPTL may also promote isoprene polymerization activity. The above results demonstrate that the present invention enables efficient production of natural rubber. [Sequence List Free Text]

[0071] SEQ ID NO: 1: Nucleotide sequence of CPT1 SEQ ID NO:2: Amino acid sequence of CPT1 SEQ ID NO: 3: Nucleotide sequence of CPT2 SEQ ID NO: 4: Amino acid sequence of CPT2 SEQ ID NO: 5: Nucleotide sequence of CPT6 SEQ ID NO: 6: Amino acid sequence of CPT6 SEQ ID NO: 7: Nucleotide sequence of CPT7 SEQ ID NO: 8: Amino acid sequence of CPT7 SEQ ID NO: 9: Base sequence of CPTL SEQ ID NO: 10: Amino acid sequence of CPTL SEQ ID NO: 11: Nucleotide sequence of REF1 SEQ ID NO: 12: Amino acid sequence of REF1 SEQ ID NO: 13: Base sequence of REF2 SEQ ID NO: 14: Amino acid sequence of REF2 SEQ ID NO: 15: Base sequence of REF8 SEQ ID NO: 16: Amino acid sequence of REF8 SEQ ID NO: 17: Nucleotide sequence of SRPP1 SEQ ID NO: 18: Amino acid sequence of SRPP1 SEQ ID NO: 19: Primer 1 (for obtaining CPT1 gene) SEQ ID NO: 20: Primer 2 (for obtaining CPT1 gene) SEQ ID NO: 21: Primer 3 (for obtaining CPT2 gene) SEQ ID NO: 22: Primer 4 (for obtaining CPT2 gene) SEQ ID NO: 23: Primer 5 (for obtaining CPT6 gene) SEQ ID NO: 24: Primer 6 (for obtaining CPT6 gene) SEQ ID NO: 25: Primer 7 (for obtaining CPT7 gene) SEQ ID NO: 26: Primer 8 (for obtaining CPT7 gene) SEQ ID NO: 27: Primer 9 (for obtaining CPTL gene) SEQ ID NO: 28: Primer 10 (for obtaining CPTL gene) SEQ ID NO: 29: Primer 11 (for obtaining REF1 gene) SEQ ID NO: 30: Primer 12 (for obtaining REF1 gene) SEQ ID NO: 31: Primer 13 (for obtaining REF2 gene) SEQ ID NO: 32: Primer 14 (for obtaining REF2 gene) SEQ ID NO: 33: Primer 15 (for obtaining REF8 gene) SEQ ID NO: 34: Primer 16 (for obtaining REF8 gene) SEQ ID NO: 35: Primer 17 (for obtaining SRPP1 gene) SEQ ID NO: 36: Primer 18 (for obtaining SRPP1 gene)

Claims

1. (A-1) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 6, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 6 and having an activity similar to that of CPT6, or (A-2) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 8 and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 8 and having an activity similar to that of CPT7; (B) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 10 and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 10 and having an activity similar to that of CPTL; A lipid membrane construct which is a proteoliposome containing a protein composition having isoprene polymerization activity, comprising:

2. (A-1) is, a protein encoded by one or more polynucleotides (a-1) selected from a polynucleotide comprising the base sequence of SEQ ID NO:5 and a polynucleotide comprising a base sequence having 90% or more identity with the base sequence of SEQ ID NO:5, the polynucleotide encoding a protein having activity similar to that of CPT6; (A-2) is, A protein encoded by one or more polynucleotides (a-2) selected from a polynucleotide comprising the base sequence of SEQ ID NO: 7 and a polynucleotide comprising a base sequence having 90% or more identity with the base sequence of SEQ ID NO: 7, the polynucleotide encoding a protein having an activity similar to that of CPT7; and (B) The protein is encoded by one or more polynucleotides (b) selected from a polynucleotide comprising the base sequence of SEQ ID NO:9 and a polynucleotide comprising a base sequence having 90% or more identity to the base sequence of SEQ ID NO:9, and encoding a protein having activity similar to that of CPTL. The construct according to claim 1, which is at least one of the following:

3. The construct of claim 1 or 2, further comprising a CPT family protein other than CPT6, 7 and CPTL, a REF family protein, and an SRPP family protein.

4. The protein composition comprises: (C) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 2, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 2 and having an activity similar to that of CPT1; (D) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 4, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 4 and having an activity similar to that of CPT2; (E) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 12, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 12 and having an activity similar to that of REF1; (F) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 14, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 14 and having an activity similar to that of REF2; (G) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 16, and a protein comprising an amino acid sequence having 90% or more identity to the amino acid sequence of SEQ ID NO: 16 and having an activity similar to that of REF8; and (H) one or more proteins selected from a protein comprising the amino acid sequence of SEQ ID NO: 18, and a protein comprising an amino acid sequence having 90% or more identity with the amino acid sequence of SEQ ID NO: 18 and having activity similar to that of SRPP1. The construct of claim 1, further comprising at least one selected from the group consisting of:

5. (C) a protein encoded by one or more polynucleotides (c) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:1 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:1, the polynucleotide encoding a protein having activity similar to that of CPT1; (D) is a protein encoded by one or more polynucleotides (d) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 3, and encoding a protein having activity similar to that of CPT2; (E) is a protein encoded by one or more polynucleotides (e) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:11 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:11 and encoding a protein having activity similar to that of REF1; (F) a protein encoded by one or more polynucleotides (f) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 13 and encoding a protein having activity similar to that of REF2; (G) A protein encoded by one or more polynucleotides (g) selected from a polynucleotide comprising the base sequence of SEQ ID NO: 15 and a polynucleotide comprising a base sequence having 90% or more identity to the base sequence of SEQ ID NO: 15, and encoding a protein having activity similar to that of REF8; and (H) is a protein encoded by one or more polynucleotides (h) selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17 and a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 17, and encoding a protein having activity similar to that of SRPP1; The construct according to claim 4, which is at least one of the following:

6. The construct according to any one of claims 1 to 5, wherein at least one of the proteins (A) to (H) is a protein derived from a rubber tree.

7. The lipid membrane construct according to any one of claims 1 to 6, wherein the proteoliposome contains a phospholipid.

8. The construct of claim 7 , wherein the phospholipid is a soybean-derived phospholipid.

9. The construct according to any one of claims 1 to 8, wherein the diameter of the proteoliposome is between 50 and 300 nm.

10. A method for producing the lipid membrane construct according to any one of claims 1 to 9, comprising expressing a polynucleotide encoding a protein constituting a composition contained in the construct according to any one of claims 1 to 9 in a cell-free protein production system in the presence of a raw material containing a phospholipid.

11. The polynucleotide encoding a protein constituting the composition contained in the construct according to any one of claims 1 to 9 is (a-1) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO:5, and a polynucleotide comprising a nucleotide sequence having 90% or more identity with the nucleotide sequence of SEQ ID NO:5, which encodes a protein having an activity similar to that of CPT6; or (a-2) one or more polynucleotides selected from a polynucleotide comprising the base sequence of SEQ ID NO: 7 and a polynucleotide comprising a base sequence having 90% or more identity with the base sequence of SEQ ID NO: 7, which encodes a protein having an activity similar to that of CPT7; (b) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 9, and a polynucleotide encoding a protein having an activity similar to that of CPTL, the polynucleotide comprising a polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

9. A method for producing the lipid membrane construct according to claim 10, comprising the steps of:

12. The polynucleotide is a polynucleotide encoding a protein constituting the composition contained in the construct according to claim 3 or 4, (c) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 1, and a polynucleotide encoding a protein having activity similar to that of CPT1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

1. (d) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3, and a polynucleotide encoding a protein having activity similar to that of CPT2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

3. (e) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 11, and a polynucleotide encoding a protein having an activity similar to that of REF1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

11. (f) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 13, and a polynucleotide encoding a protein having activity similar to that of REF2, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

13. (g) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 15, and a polynucleotide encoding a protein having an activity similar to that of REF8, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO: 15, and (h) one or more polynucleotides selected from a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 17, and a polynucleotide encoding a protein having activity similar to that of SRPP1, the polynucleotide comprising a nucleotide sequence having 90% or more identity to the nucleotide sequence of SEQ ID NO:

17. The method for producing a lipid membrane construct according to claim 10 or 11, further comprising at least one of the following steps:

13. A method for producing an isoprene polymerized compound, comprising carrying out an isoprene polymerization reaction using the construct according to any one of claims 1 to 9.

14. The method according to claim 13, wherein the isoprene polymerization reaction is carried out using a low molecular weight allyl compound as a substrate.

15. A construct according to claims 1 to 9, and Low molecular weight allyl compounds A kit for producing an isoprene polymerized compound, comprising:

16. A method for producing rubber, comprising producing rubber by using an isoprene polymer compound produced by the method for producing rubber according to claim 13 or 14.

Images