| Content Provider |
World Health Organization (WHO)-Global Index Medicus |
| Author |
Hokamura, Ayaka Wakida, Izumi Miyahara, Yuki Tsuge, Takeharu Shiratsuchi, Hideki Tanaka, Kenji Matsusaki, Hiromi |
| Description |
Country affiliation: Japan Author Affiliation: Hokamura A ( Department of Food and Health Sciences, Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, 3-1-100 Tsukide, Higashi-ku, Kumamoto 862-8502, Japan.); Wakida I ( Department of Food and Health Sciences, Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, 3-1-100 Tsukide, Higashi-ku, Kumamoto 862-8502, Japan.); Miyahara Y ( Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502, Japan.); Tsuge T ( Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502, Japan.); Shiratsuchi H ( Department of Food and Health Sciences, Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, 3-1-100 Tsukide, Higashi-ku, Kumamoto 862-8502, Japan.); Tanaka K ( Department of Biological and Environmental Chemistry, Faculty of Humanity-Oriented Sciences and Engineering, Kinki University, Kayanomori, Iizuka-shi, Fukuoka 820-8555, Japan.); Matsusaki H ( Department of Food and Health Sciences, Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, 3-1-100 Tsukide, Higashi-ku, Kumamoto 862-8502, Japan. Electronic address: matusaki@pu-kumamoto.ac.jp.) |
| Abstract |
The polyhydroxyalkanoate (PHA) copolymers consisting of short-chain-length (scl) and medium-chain-length (mcl) monomers have various properties ranging from stiff to flexible depending on the molar fraction of the monomer compositions. It has been reported that PhaG, which is first known as a (R)-3-hydroxyacyl-acyl carrier protein (ACP)-CoA transferase, actually functions as a 3-hydroxyacyl-ACP thioesterase, and the product of PP0763 gene from Pseudomonas putida KT2440 has a (R)-3-hydroxyacyl (3HA)-CoA ligase activity (Wang et al., Appl. Environ. Microbiol., 78, 519-527, 2012). In this study, we found a new (R)-3HA-CoA ligase (the product of PA3924 gene) from Pseudomonas aeruginosa PAO. The PA3924 gene was coexpressed with PHA synthase 1 gene (phaC1Ps) and phaGPs gene from Pseudomonas sp. 61-3, and ß-ketothiolase gene (phbARe) and acetoacetyl-CoA reductase gene (phbBRe) from Ralstonia eutropha in Escherichia coli LS5218 at 25°C. As a result, the copolymer containing 94.6 mol% 3-hydroxybutyrate (3HB) and 5.4 mol% mcl-3-hydroxyalkanoates (3HA) consisting of C8, C10, C12 and C14 was synthesized by recombinant E. coli LS5218 from glucose as the sole carbon source. The concentration of P(3HB-co-3HA) (scl-co-mcl-PHA) synthesized by the recombinant E. coli LS5218 harboring phaC1Ps, phaGPs, phbABRe and the PA3924 genes was approximately 7-fold higher than that of the recombinant LS5218 harboring phaC1Ps, phaGPs, phbABRe and the PP0763 genes. The number-average molecular weight of the P(3HB-co-5.4% 3HA) copolymer was 233 × 10(3), which was relatively high molecular weight. In addition, the physical and the mechanical properties of the copolymer were demonstrated to improve the brittleness of P(3HB) homopolymer. |
| File Format |
HTM / HTML |
| ISSN |
13891723 |
| Issue Number |
3 |
| Volume Number |
120 |
| e-ISSN |
13474421 |
| Journal |
Journal of Bioscience and Bioengineering |
| Language |
English |
| Publisher |
Elsevier |
| Publisher Date |
2015-09-01 |
| Publisher Place |
Japan |
| Access Restriction |
One Nation One Subscription (ONOS) |
| Subject Keyword |
Discipline Biomedical Engineering Discipline Microbiology Biopolymers Biosynthesis Escherichia Coli Genetics Metabolism Glucose Polyesters Chemistry 3-hydroxybutyric Acid Acyltransferases Alcohol Oxidoreductases Coenzyme A Ligases Cupriavidus Necator Enzymology Hydroxybutyrates Molecular Weight Pseudomonas Journal Article Research Support, Non-u.s. Gov't |
| Content Type |
Text |
| Resource Type |
Article |
| Subject |
Bioengineering Applied Microbiology and Biotechnology Biotechnology |
