首页> 外文期刊>Journal of Bioscience and Bioengineering >In vitro synthesis of polyhydroxyalkanoates using thermostable acetyl-CoA synthetase, CoA transferase, and PHA synthase from thermotorelant bacteria
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In vitro synthesis of polyhydroxyalkanoates using thermostable acetyl-CoA synthetase, CoA transferase, and PHA synthase from thermotorelant bacteria

机译:使用热稳定的细菌中的热稳定的乙酰辅酶A合成酶,辅酶A转移酶和PHA合成酶体外合成聚羟基链烷酸酯

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Thermostable enzymes are required for the rapid and sustainable production of polyhydroxyalkanoate (PHA) in vitro. The in vitro synthesis of PHA using the engineered thermostable synthase PhaC1(SG)(STQK) has been reported; however, the non-thermostable enzymes acetyl-CoA synthetase (ACS) and CoA transferase (CT) from mesophilic strains were used as monomer-supplying enzymes in this system. In the present study, acs and ct were cloned from the thermophilic bacteria Pelotomaculum thermopropionicum JCM10971 and Thermus thermophilus JCM10941 to construct an in vitro PHA synthesis system using only thermostable enzymes. ACS from P. thermopropionicum (ACS(Pt)) and CT from I thermophilus (CTTt) were confirmed to have high thermostability, and their optimal temperatures were around 60 degrees C and 75 degrees C, respectively. The in vitro PHA synthesis was successfully performed by ACS(Pt), CTTt, PhaC1(SG)(STQK), and poly(3-hydroxybutyrate) [P(3HB)] was synthesized at 45 degrees C. Furthermore, the yields of P(3HB) and P(lactate-co-3HB) at 37 degrees C were 1.4-fold higher than those of the in vitro synthesis system with non-thermostable ACS and CT from mesophilic strains. Overall, the thermostable ACS and CT were demonstrated to be useful for the efficient in vitro PHA synthesis at relatively high temperatures. (C) 2016, The Society for Biotechnology, Japan. All rights reserved.
机译:在体外快速且可持续地生产聚羟基链烷酸酯(PHA)需要热稳定酶。已经报道了使用工程热稳定合酶PhaC1(SG)(STQK)体外合成PHA的方法。然而,来自嗜温菌株的非恒温酶乙酰辅酶A合成酶(ACS)和辅酶A转移酶(CT)被用作该系统中的单体供应酶。在本研究中,从嗜热细菌Petroomaculum thermopropionicum JCM10971和Thermus thermophilus JCM10941克隆了acs和ct,以仅使用热稳定酶构建体外PHA合成系统。证实了丙酸热丙酸杆菌的ACS(ACS(Pt))和嗜热嗜热杆菌的CT(CTTt)具有很高的热稳定性,它们的最佳温度分别为60摄氏度和75摄氏度。通过ACS(Pt),CTTt,PhaC1(SG)(STQK)成功地进行了体外PHA合成,并在45摄氏度下合成了聚(3-羟基丁酸酯)[P(3HB)]。此外,P的收率(3HB)和P(乳酸-co-3HB)在37摄氏度时比具有嗜温菌株的非恒温ACS和CT的体外合成系统高1.4倍。总体而言,热稳定的ACS和CT被证明可用于在相对较高的温度下有效地进行体外PHA合成。 (C)2016年,日本生物技术学会。版权所有。

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