Lu Qiuhe, Han Jing, Zhou Ligang, Zhou Jian, Xiang Hua
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Datun Road, Chaoyang District, Beijing 100101, Peoples Republic of China.
J Bacteriol. 2008 Jun;190(12):4173-80. doi: 10.1128/JB.00134-08. Epub 2008 Apr 11.
The haloarchaeon Haloferax mediterranei has shown promise for the economical production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), a desirable bioplastic. However, little is known at present about the genes involved in PHBV synthesis in the domain Archaea. In this study, we cloned the gene cluster (phaEC(Hme)) encoding a polyhydroxyalkanoate (PHA) synthase in H. mediterranei CGMCC 1.2087 via thermal asymmetric interlaced PCR. Western blotting revealed that the phaE(Hme) and phaC(Hme) genes were constitutively expressed, and both the PhaE(Hme) and PhaC(Hme) proteins were strongly bound to the PHBV granules. Interestingly, CGMCC 1.2087 could synthesize PHBV in either nutrient-limited medium (supplemented with 1% starch) or nutrient-rich medium, up to 24 or 18% (wt/wt) in shaking flasks. Knockout of the phaEC(Hme) genes in CGMCC 1.2087 led to a complete loss of PHBV synthesis, and only complementation with the phaEC(Hme) genes together (but not either one alone) could restore to this mutant the capability for PHBV accumulation. The known haloarchaeal PhaC subunits are much longer at their C termini than their bacterial counterparts, and the C-terminal extension of PhaC(Hme) was proven to be indispensable for its function in vivo. Moreover, the mixture of purified PhaE(Hme)/PhaC(Hme) (1:1) showed significant activity of PHA synthase in vitro. Taken together, our results indicated that a novel member of the class III PHA synthases, composed of PhaC(Hme) and PhaE(Hme), accounted for the PHBV synthesis in H. mediterranei.
嗜盐古菌地中海嗜盐嗜盐放线菌已显示出有望经济地生产聚(3-羟基丁酸酯-co-3-羟基戊酸酯)(PHBV),这是一种理想的生物塑料。然而,目前对于古菌域中参与PHBV合成的基因知之甚少。在本研究中,我们通过热不对称交错PCR克隆了地中海嗜盐放线菌CGMCC 1.2087中编码聚羟基脂肪酸酯(PHA)合酶的基因簇(phaEC(Hme))。蛋白质免疫印迹分析表明phaE(Hme)和phaC(Hme)基因组成性表达,并且PhaE(Hme)和PhaC(Hme)蛋白都与PHBV颗粒紧密结合。有趣的是,CGMCC 1.2087在营养限制培养基(补充1%淀粉)或营养丰富的培养基中都能合成PHBV,在摇瓶中产量分别高达24%或18%(重量/重量)。敲除CGMCC 1.2087中的phaEC(Hme)基因导致PHBV合成完全丧失,只有同时互补phaEC(Hme)基因(而不是单独一个基因)才能使该突变体恢复PHBV积累能力。已知的嗜盐古菌PhaC亚基在其C末端比细菌对应物长得多,并且已证明PhaC(Hme)的C末端延伸对于其体内功能是不可或缺的。此外,纯化的PhaE(Hme)/PhaC(Hme)(1:1)混合物在体外显示出显著的PHA合酶活性。综上所述,我们的结果表明由PhaC(Hme)和PhaE(Hme)组成的III类PHA合酶新成员负责地中海嗜盐放线菌中的PHBV合成。