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科研成果

论文题目:	A patatin-like protein associated with the polyhydroxyalkanoate (PHA) granules of Haloferax mediterranei acts as an efficient depolymerase in degradation of native PHA
作者:	Liu Guiming Hou Jing, Cai Shuangfeng, Zhao Dahe, Cai Lei, Han Jing, Zhou Jian, Xiang Hua*.
联系作者:
刊物名称:	Appl Environ Microbiol
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年份:	2015
影响因子:	4.486
论文下载:	下载地址
摘要:	The key enzymes and pathways involved in polyhydroxyalkanoate (PHA) biosynthesis in haloarchaea have been identified in recent years, but the haloarchaeal enzymes for PHA degradation remain unknown. In this study, a patatin-like PHA depolymerase, PhaZh1, was determined to be located on the PHA granules in the haloarchaeon Haloferax mediterranei. PhaZh1 hydrolyzed the native PHA (nPHA, including nPHB and nPHBV in this study) granules in vitro with 3-hydroxybutyrate (3HB) monomer as the primary product. The site-directed mutagenesis of PhaZh1 indicated that Gly16, Ser47 (in a classical lipase box G-X-S47-X-G) and Asp195 of this depolymerase were essential for its activity in nPHA granule hydrolysis. Notably, phaZh1 and bdhA (encoding putative 3HB dehydrogenase) form a gene cluster (HFX_6463-6464) in H. mediterranei. The 3HB monomer generated from nPHA degradation by the PhaZh1 could be further converted into acetoacetate by BdhA, indicating that PhaZh1-BdhA may constitute the first part of a PHA degradation pathway in vivo. Interestingly, although PhaZh1 showed efficient activity and was most likely the key enzyme in nPHA granule hydrolysis in vitro, the knockout of phaZh1 had no significant effect on the intracellular PHA mobilization, implying the existence of alternative PHA mobilization pathway(s) that function effectively within the cells of H. mediterranei. Therefore, identification of this patatin-like depolymerase of haloarchaea may provide a new strategy for producing the high value-added chiral compound (R)-3HB, and may also shed light on the PHA mobilization in haloarchaea.