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Biosynthesis of polylactic acid and its copolymers using evolved propionate CoA transferase and PHA synthase

✍ Scribed by Taek Ho Yang; Tae Wan Kim; Hye Ok Kang; Sang-Hyun Lee; Eun Jeong Lee; Sung-Chul Lim; Sun Ok Oh; Ae-Jin Song; Si Jae Park; Sang Yup Lee


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
462 KB
Volume
105
Category
Article
ISSN
0006-3592

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✦ Synopsis


Abstract

For the synthesis of polylactic acid (PLA) and its copolymers by one‐step fermentation process, heterologous pathways involving Clostridium propionicum propionate CoA transferase (Pct~Cp~) and Pseudomonas sp. MBEL 6‐19 polyhydroxyalkanoate (PHA) synthase 1 (PhaC1~__Ps__6‐19~) were introduced into Escherichia coli for the generation of lactyl‐CoA endogenously and incorporation of lactyl‐CoA into the polymer, respectively. Since the wild‐type PhaC1~__Ps__6‐19~ did not efficiently accept lactyl‐CoA as a substrate, site directed mutagenesis as well as saturation mutagenesis were performed to improve the enzyme. The wild‐type Pct~Cp~ was not able to efficiently convert lactate to lactyl‐CoA and was found to exert inhibitory effect on cell growth, random mutagenesis by error‐prone PCR was carried out. By employing engineered PhaC1~__Ps__6‐19~ and Pct~Cp~, poly(3‐hydroxybutyrate‐co‐lactate), P(3HB‐co‐LA), containing 20–49 mol% lactate could be produced up to 62 wt% from glucose and 3HB. By controlling the 3HB concentration in the medium, PLA homopolymer and P(3HB‐co‐LA) containing lactate as a major monomer unit could be synthesized. Also, P(3HB‐co‐LA) copolymers containing various lactate fractions could be produced from glucose alone by introducing the Cupriavidus necator β‐ketothiolase and acetoacetyl‐CoA reductase genes. Fed‐batch cultures were performed to produce P(3HB‐co‐LA) copolymers having 9–64 mol% of lactate, and their molecular weights, thermal properties, and melt flow properties were determined. Biotechnol. Bioeng. 2010; 105: 150–160. © 2009 Wiley Periodicals, Inc.


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Biosynthesis of Polyhydroxyalkanoate (PH
✍ Takeharu Tsuge; Kotaro Yano; Shin-ichi Imazu; Keiji Numata; Yoshihiro Kikkawa; H 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB

## Abstract Summary: Eleven laboratory‐evolved polyhydroxyalkanoate (PHA) synthases which originated from __Pseudomonas__ sp. 61‐3 enzyme (PhaC1~Ps~), together with the wild‐type enzyme, were applied for PHA synthesis from fructose using __Ralstonia eutropha__ PHB^‐^4 as a host strain. The evolved