Phytase enzymes, nucleic acids encoding phytase enzymes and vectors and host cells incorporating same

Inactive Publication Date: 2006-02-23
STAFFORD CHRISTIAN +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Benefits of technology

[0107] Another advantage of the present invention is that, by virtue of providing a polynucleotide encoding a protein having phytase activity, it is possible to produce through recombinant means a host cell which is capable of producing the protein having phytase activity in relatively large quantities.
[0108] Yet another advantage of the present invention is that commercial application of proteins having phytase activity is made practical. For example, the present invention provides animal feed incorpora

Problems solved by technology

The bioavailability of phosphorus in this form is generally quite low for non-ruminants, such as poultry and swine, because they lack digestive enzymes for separating phosphorus from the phytate molecule.
For example, expense is incurred when inorganic phosphorus (e.g., dicalcium phosphate, defluorinated phosphate) or animal products (e.g., meat and bone meal, fish meal) are added to

Method used

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  • Phytase enzymes, nucleic acids encoding phytase enzymes and vectors and host cells incorporating same
  • Phytase enzymes, nucleic acids encoding phytase enzymes and vectors and host cells incorporating same
  • Phytase enzymes, nucleic acids encoding phytase enzymes and vectors and host cells incorporating same

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Effect test

example 1

Evidence of Phytate Hydrolysing Activity in Liquid Culture

[0191]P. piceum (ATCC No. 10519) and P. hordei (ATCC No. 22053) were grown in defined media containing various concentrations of inorganic phosphate, and growth characteristics and phytase production were assayed and compared. Spore suspensions were used (2×106 spores / ml final con) to inoculate a minimal media (Vogels) where the phosphate concentration was altered to see how this would affect growth and phytase production. Cultures were grown in 50 ml of medium in shake flask culture at 25° C. (P. hordei) or 30° C. (P. piceum). Cultures were harvested at 24, 48, 72 and 96 hours. Cultures supernatants were assayed for phytase activity using the method of Fiske and SubbaRow. Growth was determined by dry weight (P. hordei) or OD readings (P. piceum).

1A. Effect of Different Media Conditions on Growth and Morphology

[0192] The series of Penicillium growth curves that were produced, such as the P. piceum growth curve of FIG. 3 a...

example 2

PCR Amplification of Phytase Gene Fragments

2A. Degenerate Primer Design

[0209] Based on alignments of published phytase amino acid sequences, a range of degenerate primers were designed against conserved structural and catalytic regions. Such regions included those that were highly conserved among the phytases, as well as those known to be important for enzyme structure and function.

[0210] In one study, amino acid sequences for 4 published phytases were aligned. The sequences were of phytases from: (i) A. niger (DEFINITION: A. niger phyA gene.; ACCESSION: Z16414; van Hartingsveldt, W., et al, 1992); (ii) A. fumigatus (DEFINITION: Aspergillus fumigatus phytase gene, complete cds.; ACCESSION: U59804; Pasamontes, L., et al, 1997); (iii) A. terreus (DEFINITION: Aspergillus terreus 9A1 phytase gene, complete cds.; ACCESSION: U59805; Mitchell, D. B., et al, 1997); and (iv) Myceliophtora thermophilus (DEFINITION: Myceliophthora thermophila phytase gene, complete cds.; ACCESSION: U59806;...

example 3

Southern Analysis for Library Production

[0223] Genomic DNA from P. hordei, P. piceum and A. niger were digested with a range of restriction enzymes overnight at 37° C. Successfully digested DNA was run out on a 1% agarose gel in preparation for transfer to the nylon membrane. After completion of electrophoresis, the agarose gel was soaked for 10 min. in 0.2M HCl to depurinate the DNA and then rinsed briefly in ddH2O. The DNA was transferred to the Hybond™-N+ membrane (Amersham International PLC) by alkali capillary blotting. The blot was set up so that the nylon filter was sandwiched between the gel and a stack of absorbent paper towels. A wick of Whatman 3MM paper (Schleicher and Schuell, Dassel, Germany) was prepared on a glass plate over a reservoir of transfer buffer (0.4M NaOH). The gel was inverted on the wick, taking care to avoid the formation of air bubbles, and surrounded by strips of Nescofilm to prevent the blotting action of the paper towels from by-passing the gel at ...

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Abstract

A novel DNA is provided which encodes an enzyme having phytase activity isolated from Penicillium. Also provided for is a method of isolating DNA encoding an enzyme having phytase activity from organisms which possess such DNA, transformation of the DNA into a suitable host organism, expression of the transformed DNA and the use of the expressed phytase protein in feed as a supplement.

Description

RELATED APPLICATIONS [0001] The present application claims priority to U.S. Provisional Patent Application No. 60 / 148,960 filed Aug. 13, 1999, which is hereby incorporated by reference in its entirety.FIELD OF THE INVENTION [0002] The present invention relates to phytase, nucleic acids encoding phytase, as well as the production of phytase and its use. REFERENCES [0003] Altschul, S. F., Gish, W., Miller, W., Myers, E. W. & Lipman, D. J. (1990) “Basic local alignment search tool.” J. Mol. Biol. 215:403-410. [0004] Altschul, S. F., Madden, T. L., Schäffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.” Nucleic Acids Res. 25:3389-3402. [0005] Ausubel et al. (eds.), Current Protocols In Molecular Biology, Vol. 1, John Wiley & Sons, Inc. 1987. [0006] Benton, W. and Davis, R., 1977, Science 196:180. [0007] Berger and Kimmel, 1987, Guide to Molecular Cloning Techniques, Methods in Enzymology...

Claims

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Application Information

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IPC IPC(8): C07H21/04C12N9/16C12N1/16A23K1/165A23L33/00C12N1/19C12N15/09C12N15/55C12P7/22
CPCC12P7/22C12N9/16C12N15/52
Inventor STAFFORD, CHRISTIANTRINCI, ANTHONYBROOKMAN, JAYNE
Owner STAFFORD CHRISTIAN
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