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Methods of developing terpene synthase variants

a technology of terpene synthase and terpene, which is applied in the field of developing terpene synthase variants, can solve the problems of limiting the kinetic capacity required for efficient production of terpenes in engineered microbial hosts, unable to improve the kinetic capacity of terpene synthases, and the application of conventional protein engineering strategies such as directed evolution, which is devoid of terpene synthases. , to achiev

Active Publication Date: 2012-08-02
AMYRIS INC
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  • Abstract
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AI Technical Summary

Benefits of technology

[0010]The present disclosure relates to methods of developing terpene synthase variants through engineered host cells. Particularly, the disclosure provides methods of developing terpene synthase variants with improved in vivo performance. The methods also allow for the continued improvement of the in vivo performance of these enzymes.

Problems solved by technology

However, because they are slow enzymes, terpene synthases are often the bottlenecks in the metabolic pathways.
In addition, they can suffer from other shortcomings such as substrate inhibition that limit the kinetic capacity required for efficient production of terpenes in engineered microbial hosts (Crock et al.
However, these studies have fallen short of improving the kinetic capacity of terpene synthases while also maintaining their product specificity.
In addition, the application of conventional protein engineering strategies, such as directed evolution, has been devoid for terpene synthases primarily because of the lack of available and effective high throughput screening methods (Yoshikuni et al.

Method used

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  • Methods of developing terpene synthase variants
  • Methods of developing terpene synthase variants
  • Methods of developing terpene synthase variants

Examples

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example 1

[0200]This example describes methods for making DNA constructs useful in the generation and characterization of terpene synthase variants.

[0201]Expression plasmid pAM36-MevT66 was generated by inserting the MevT66 operon into vector pAM36. Vector pAM36 was generated by removing the tet resistance gene from and adding an oligonucleotide cassette containing AscI-SfiI-AsiSI-XhoI-PacI-FslI-PmeI restriction sites into the pACYC184 vector (GenBank accession number XO6403). The MevT66 operon encoded the set of MEV pathway enzymes that together transform the ubiquitous precursor acetyl-CoA to (R)-mevalonate, namely acetoacetyl-CoA thiolase, HMG-CoA synthase, and HMG-CoA reductase. The MevT66 operon was synthetically generated and comprised the atoB gene of Escherichia coli (GenBank accession number NC—000913 REGION: 2324131 . . . 2325315; encodes an acetoacetyl-CoA thiolase) codon-optimized for expression in Escherichia coli, the coding sequence of the ERG13 gene of Saccharomyces cerevisiae...

example 2

[0234]This example describes methods for making yeast strains useful in the generation and characterization of terpene synthases variants.

[0235]Strains Y93 (MAT A) and Y94 (MAT alpha) were generated by replacing the promoter of the ERG9 gene of yeast strains Y002 and Y003 (CEN.PK2 background MAT A or MAT alpha, respectively; ura3-52; trp1-289; leu2-3,112; his3Δ1; MAL2-8C; SUC2; van Dijken et al. (2000) Enzyme Microb. Technol. 26:706-714), respectively, with the promoter of the MET3 gene of Saccharomyces cerevisia. To this end, exponentially growing Y002 and Y003 cells were transformed with integration construct i8 (SEQ ID NO: 87), which comprised the kanamycin resistance marker (KanMX) flanked by the promoter and terminator of the Tef1 gene of Kluyveromyces lactis, the ERG9 coding sequence, a truncated segment of the ERG9 promoter (trune. PERG9), and the MET3 promoter (PMET3), flanked by ERG9 upstream and downstream sequences (FIG. 1A). Host cell transformants were selected on mediu...

example 3

[0283]This example demonstrates the feasibility of using FPP starvation based selection in Escherichia coli to screen for terpene synthases with improved in vivo performance.

[0284]DH5αchemical- or electro-competent Escherichia coli cells (Invitrogen, Carlsbad, Calif.) were transformed with 5 ng of an expression plasmid selected from the group consisting of expression plasmids pAM1668 (negative control), pAM1670, pAM2096, pAM2097, pAM2098, pAM2101, and pAM2104. Host cell transformants were plated on agar plates comprising carbenicillin, and the plates were incubated at 30° C. for 2-3 days.

[0285]As shown in FIG. 2, cells transformed with expression plasmid pAM2097 or pAM2096 produced colonies of similar size as cells transformed with empty vector (pAM1668). However, cells transformed with expression plasmid pAM1670, pAM2098, as well as cells transformed with expression plasmids pAM2104 or pAM2101 (data not shown), produced colonies that were smaller than those produced by the control....

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Abstract

The present disclosure relates to methods of developing terpene synthase variants through engineered host cells. Particularly, the disclosure provides methods of developing terpene synthase variants with improved in vivo performance that are useful in the commercial production of terpene products. Further encompassed in the present disclosure are superior terpene synthase variants and host cells comprising such terpene synthase variants.

Description

1. CROSS-REFERENCE TO RELATED APPLICATION[0001]This application claims the benefit of priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Ser. No. 61 / 438,948 filed Feb. 2, 2011, which is incorporated herein by reference.2. FIELD OF THE INVENTION[0002]The present disclosure relates to methods of developing terpene synthase variants through engineered host cells. Particularly, the disclosure provides methods of developing terpene synthase variants with improved in vivo performance that are useful in the commercial production of terpene products. Further encompassed in the present disclosure are superior terpene synthase variants, and host cells comprising such terpene synthase variants.3. BACKGROUND[0003]Terpenes are a large class of hydrocarbons that are produced in many organisms. They are derived by linking units of isoprene (C5H8), and are classified by the number of isoprene units present. Hemiterpenes consist of a single isoprene unit. Isoprene itself is cons...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12Q1/02
CPCC12Q1/527C12N9/88C12Y402/03047C12Q1/25C12N15/52
Inventor ZHAO, LISHANXU, LANWESTFALL, PATRICKMAIN, ANDREW
Owner AMYRIS INC
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