Mutiple gene expression for engineering novel pathways and hyperexpression of foreign proteins in plants

a technology of foreign protein and gene expression, applied in the field of mutation gene expression for engineering novel pathways and hyperexpression of foreign proteins in plants, can solve the problems of increasing the toxicity of organomercurials, threatening the safety, and other techniques, such as mechanical and bacterial bioremediation, which have little success in implementation

Inactive Publication Date: 2003-02-27
UNIV OF CENT FLORIDA RES FOUND INC +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

This poses a serious problem when engineering multiple genes in plants.
In the past other techniques, such as mechanical and bacterial bioremediation were implemented with little success, since they were costly and threatened the safety of our environment.
Organomercurials are more toxic due to its increased hydrophobicity, which allows it to cross lipid membranes because it is more hydrophobic than mercury.
In water, mercury pollution also poses a problem.
During their life span, they can accumulate high levels of methylmercury that can reach 1.0 ppm in normal water and 30 ppm in areas of high pollution with mercury (http://ehpnet.niehs.nih.gov) Then, humans and birds feed on contaminated fish and accumulation in their tissue cause severe neurological damage.
One of the drawbacks of nuclear genetic engineerig is that it requires several back crosses to create the complete pathway that detoxifies mercury and organomercurials (Bizily et al.
Polycistrons have been observed in chloroplasts in the past but processing RNA sequences present in between individual transcripts, proteins or enzymes involved in processing or cofactors necessary for processing of polycistrons have not yet been characterized Therefore, it was not obvious to one skilled in the art that multiple foreign gene transcripts would be properly processed and translated when expressed from a heterologous promoter.
Prior to this patent application there were no published reports of expression of multiple genes in chloroplasts and there were valid reasons to suggest that it would be problematic.
Indeed, despite several reports of foreign gene expression

Method used

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  • Mutiple gene expression for engineering novel pathways and hyperexpression of foreign proteins in plants
  • Mutiple gene expression for engineering novel pathways and hyperexpression of foreign proteins in plants
  • Mutiple gene expression for engineering novel pathways and hyperexpression of foreign proteins in plants

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example 2

[0123] E. Coli Transformants. Due to the similarity of protein synthetic machinery (Brixey et al. 1997), expression of all metal resistance conferring chloroplast vectors are first tested in E. coli before their use in tobacco transformation The activity of the enzymes, mercury ion reductase (merA) and organomercurial lyase (merB) are tested by transforming E. coli (XLI-blue) with the recombinant plasmids and growing them in LB solid medium with HgCl.sub.2 (FIG. 9). The cells, control (XLI-bue), pLD-merAB and pLDmerAB-3'UTR are grown in different concentrations of Hg Cl.sub.2. Control cells do not grow even at concentrations less than 25 .mu.M Hg Cl.sub.2 but the transformed cells grow well even at 100 .mu.M HgCl.sub.2-(FIG. 10). The ability to grow at these high concentrations of mercury in which control is not able to grow, confirms the functionality of both enzymes. Control and transformed clones are grown in LB with 500 .mu.g / ml of spectinomycin for 24 hours at 37.degree. C. Whe...

example 3

[0133] Chlorella vulgaris transformation vector: The region 16S to 23S of the Chlorella vulgaris chloroplast genome is amplified by PCR using specific primers complementary to rrn16 and to rrn23. The PCR product will be cloned into pCR 2.1 vector available from Promega. The PCR product 16S to 23S is removed from the pCR2.1 vector by a blunt end restriction endonuclease and cloned into the pUC19 in which the multiple cloning site has been removed using a blunt end restriction enzyme (Pvu1I). Then the cassette containing the promoter, the antibiotic resistance gene and the merAB genes is inserted into the new vector (Chlorella transformation vector) using a blunt end restriction enzyme (HincII) that is present in the spacer region between trnA and trnT. The final construct is used for the transformation of Chlorella vulgaris (FIG. 12).

[0134] Bombardment and transformation of Chlorella vulgaris: The biolistic transformation method (Sanford et al. 1993) is optimized for transformation o...

example 4

[0138] Synechocystis transformation vector: The region 16S to 23S of the Synechocystis genome is amplified by PCR using specific primers complementary to rrn 116 and to rrn23. The PCR product is cloned into the pCR 2.1 vector available from Promega. The PCR product 16S to 23S is removed from the pCR2.1 vector by a blunt end restriction endonuclease and cloned into pUC19 in which the multiple cloning site has been removed using a blunt end restriction enzyme (Pvu1I). Then the cassette containing the promoter, the antibiotic resistance gene and the merAB genes is inserted into the new vector (Synechocystis transformation vector) using a blunt end restriction enzyme (HincII) that is present in the spacer region between trnI and trnA. The final construct will be used for the transformation of Synechocystis (FIG. 13).

[0139] Transformation of Synechocystis: A fresh culture of wild type in BG-11 (heterotrophic medium) plus glucose is grown to OD.sub.730=0.5 after 2-3 days of culture. Cells...

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Abstract

Introducing blocks of foreign genes in a single operon would avoid complications such as position effect and gene silencing inherent in putting one gene at a time into random locations in the nuclear genome. Cloning several genes into a single T-DNA does not avoid the compounded variable expression problem encountered in nuclear transgenic plants. This disclosure shows that a bacterial operon can be expressed in a single integration event as opposed to multiple events requiring several years to accomplish. Expression of multiple genes via a single transformation event opens the possibility of expressing foreign pathways or pharmaceutical proteins involving multiple genes. Expressing the Cry2aA2 operon, including a putative chaperonin to aid in protein folding, in the chloroplast via a single transformation event leads to production of crystalized insecticidal proteins. Expressing the Mer operon via a single transformation event leads to a phytoremediation system.

Description

[0001] This patent application claims the benefit of U.S. Provisional Applications Nos. 60 / 185,660, filed Feb. 29, 2000, 60 / 257,408, filed Dec. 22, 2000, 60 / 259,248 filed Dec. 29, 2000 and 60 / 266,121 filed Feb. 2, 2001. All applications are here incorporated by reference.[0003] This application pertains to the field of genetic engineering of plant genomes, particularly plastids and to methods of and engineered plants with operons that lead to and result in overexpression of the gene of interest. This application also pertains to the field of genetic engineering of algal and bacterial genomes.DESCRIPTION OF RELATED ART[0004] Karamata, in U.S. Pat. No. 4,797,279, proposed the generation of Bacillus thuringiensis hybrids that have insecticidal properties through conjugation. Conjugation is mediated by a conjugative plasmid functional in the B.t. kurstaki strain and the B.t. tenebrionis strain. The resulting hybrid is capable of producing each of the delta-endotoxin crystals typical for...

Claims

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Application Information

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IPC IPC(8): C07K14/325C12N15/74C12N15/79C12N15/82
CPCC07K14/325C12N15/74C12N15/79C12N15/8214C12N15/8216C12N15/8241C12N15/8257C12N15/8259C12N15/8271C12N15/8286Y02A40/146
Inventor DANIELL, HENRYMOAR, WILLIAM
Owner UNIV OF CENT FLORIDA RES FOUND INC
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