Ishii-Hyakutake Manami, Sakurai Tetsuo, Tsuge Takeharu
Department of Materials Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502, Japan.
Microorganisms. 2021 Sep 14;9(9):1949. doi: 10.3390/microorganisms9091949.
A high-throughput screening method based on the degree of polymerization (DP) of polyhydroxyalkanoate (PHA) was developed using high-performance liquid chromatography (HPLC). In this method, PHA production was achieved using recombinant supplemented with benzyl alcohol as a chain terminal compound. The cultured cells containing benzyl alcohol-capped PHA were decomposed by alkaline treatment, and the peaks of the decomposed monomer and benzyl alcohol were detected using HPLC. The DP of PHA could be determined from the peak ratio of the decomposed monomer to terminal benzyl alcohol. The measured DP was validated by other instrumental analyses using purified PHA samples. Using this system, mutants of PHA synthase from YB-4 (PhaRC) were screened, and some enzymes capable of producing PHA with higher DP than the wild-type enzyme were obtained. The PHA yields of two of these enzymes were equivalent to the yield of the wild-type enzyme. Therefore, this screening method is suitable for the selection of beneficial mutants that can produce high molecular weight PHAs.
利用高效液相色谱法(HPLC)开发了一种基于聚羟基脂肪酸酯(PHA)聚合度(DP)的高通量筛选方法。在该方法中,使用补充了苄醇作为链端化合物的重组菌实现PHA的生产。含苄醇封端PHA的培养细胞经碱处理分解,用HPLC检测分解后的单体和苄醇的峰。PHA的DP可由分解单体与末端苄醇的峰面积比确定。通过对纯化的PHA样品进行其他仪器分析验证了测得的DP。利用该系统,筛选了来自YB - 4的PHA合酶(PhaRC)突变体,获得了一些能够产生比野生型酶具有更高DP的PHA的酶。其中两种酶的PHA产量与野生型酶的产量相当。因此,这种筛选方法适用于选择能够产生高分子量PHA的有益突变体。