Methods and compositions for cellular and metabolic engineering

a metabolic engineering and cellular technology, applied in the field of methods and compositions for cellular and metabolic engineering, can solve the problems of unsuitable intracellular location of proteins, unsuitable folding, improper modification, etc., and achieve the effect of improving the ability to catalyz

Inactive Publication Date: 2006-11-16
MAXYGEN
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Benefits of technology

[0025] (4) screening at least one further recombinant gene from the further library of recombinant genes that confers enhanced ability to catalyze the second reaction of interest in the cell relative to a previous recombinant gene;

Problems solved by technology

Bailey (Science 252:1668-1674 (1991)) describes the application of metabolic engineering to the recruitment of heterologous genes for the improvement of a strain, with the caveat that such introduction can result in new compounds that may subsequently undergo further reactions, or that expression of a heterologous protein can result in proteolysis, improper folding, improper modification, or unsuitable intracellular location of the protein, or lack of access to required substrates.

Method used

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  • Methods and compositions for cellular and metabolic engineering

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examples

I. Alteration of Enzyme Activity and Specificity.

[0208] In this example, recursive sequence recombination techniques of the instant invention were used to expand the range of substrates efficiently hydrolyzed by E. coli β-galactosidase. The goal was to evolve wild type E. coli β-galactosidase into a fucosidase. The enzyme showed very weak activity with both ρ-nitrophenyl-β-D-fucopyranoside and o-nitrophenyl-β-D-fucopyranoside (estimated respectively as 80- and 160-fold less efficient than for ρ-nitrophenyl-β-D-galactopyranoside).

[0209] To increase the activity of E. coli β-galactosidase against these fucopyranoside derivatives, a lacZ gene (a 3.8 kb Hind III-BamHI fragment from plasmid pCH110, Pharmacia) encoding E. coli β-galactosidase was subcloned into plasmid p18SFI-BLA-SFI (Stemmer, Nature, 370:389-391 (1994)). The resulting plasmid, p18-lacZ, was used for recursive sequence recombination and mutant screening.

[0210] Purified plasmid p18-lacZ (4-5 μg) was used directly for D...

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Abstract

The present invention is generally directed to the evolution of new metabolic pathways and the enhancement of bioprocessing through a process herein termed recursive sequence recombination. Recursive sequence recombination entails performing iterative cycles of recombination and screening or selection to “evolve” individual genes, whole plasmids or viruses, multigene clusters, or even whole genomes. Such techniques do not require the extensive analysis and computation required by conventional methods for metabolic engineering.

Description

[0001] This application is a continuation-in-part of U.S. patent application Ser. No. 08 / 198,431, filed Feb. 17, 1994, Serial No. PCT / US95 / 02126, filed, Feb. 17, 1995, Ser. No. 08 / 537,874, filed Oct. 30, 1995, Ser. No. 08 / 621,859, filed Mar. 25, 1996, Ser. No. 08 / 621,430, filed Mar. 25, 1996, and Ser. No. 08 / 425,684, filed Apr. 18, 1995, the specifications of which are herein incorporated by reference in their entirety for all purposes.BACKGROUND OF THE INVENTION [0002] Metabolic engineering is the manipulation of intermediary metabolism through the use of both classical genetics and genetic engineering techniques. Cellular engineering is generally a more inclusive term referring to the modification of cellular properties. Cameron et al. (Applied Biochem. Biotech. 38:105-140 (1993)) provide a summary of equivalent terms to describe this type of engineering, including “metabolic engineering”, which is most often used in the context of industrial microbiology and bioprocess engineerin...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C40B30/06C40B40/08
CPCC12N15/1058C12N15/1027
Inventor MINSHULL, JEREMYSTEMMER, WILLEM
Owner MAXYGEN
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