Gerngross T U, Snell K D, Peoples O P, Sinskey A J, Csuhai E, Masamune S, Stubbe J
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139-4307.
Biochemistry. 1994 Aug 9;33(31):9311-20. doi: 10.1021/bi00197a035.
Polyhydroxyalkanoate (PHA) synthase has been expressed in Escherichia coli by reengineering the 5'-end of the wild-type (wt) gene and subsequent transformation of this gene into protease-deficient E. coli UT5600 (ompT-). Induction with IPTG results in soluble PHA synthase, which is approximately 5% of the total protein. The soluble synthase has been purified to > 90% homogeneity using FPLC chromatography on hydroxylapatite and Q-Sepharose and has a specific activity of 5 mumol min-1 mg-1. The molecular weight of the PHA product is approximately 10(6) Da based on PlGel chromatography and calibration using polystyrene molecular weight markers. The synthase in the absence of substrate appears to exist in both monomeric and dimeric forms. Incubation of the synthase with an excess of substrate converts it into a form that is now extractable into CHCl3 and sediments on sucrose density ultracentrifugation with PHA. Studies in which the ratio of substrate, 3-D-hydroxybutyrylCoA, to synthase is varied suggest that during polymerization the elongation process occurs at a rate much faster than during the initiation process. A mechanistic model has been proposed for the polymerization process [Griebel, R., Smith, Z., & Merrick, J. (1968) Biochemistry 7, 3676-3681] in which two cysteines are required for catalysis. This model is based on the well-characterized enzymes involved in fatty acid biosynthesis. To test this model, several site-directed mutants of synthase, selected based on sequence conservation among synthases, have been prepared. The C459S mutant has activity approximately 90% that of the wt protein, while the C319S and C319A synthases possess < 0.01% the activity of the wt protein. CD and antibody studies suggest that the mutant proteins are properly folded. The detection of only a single essential cysteine by mutagenesis and the requirement for posttranslational modification by phosphopantetheine to provide a second thiol in many enzymes utilizing coenzyme A thiol ester substrates made us consider the possibility that posttranslational modification was required for synthase activity as well. This hypothesis was confirmed when the plasmid containing PHA synthase (pKAS4) was transformed into E. coli SJ16, requiring beta-alanine for growth. Growth of SJ16/pKAS4 on [3H]-beta-alanine followed by Coomassie staining of the protein and autoradiography revealed that PHA synthase is overexpressed and that beta-alanine is incorporated into the protein. These results suggest PHA synthase is posttranslationally modified by phosphopantetheine.(ABSTRACT TRUNCATED AT 400 WORDS)
通过对野生型(wt)基因的5'端进行改造,并随后将该基因转化到蛋白酶缺陷型大肠杆菌UT5600(ompT-)中,聚羟基链烷酸酯(PHA)合酶已在大肠杆菌中得到表达。用异丙基-β-D-硫代半乳糖苷(IPTG)诱导可产生可溶性PHA合酶,其含量约占总蛋白的5%。利用羟基磷灰石和Q-琼脂糖凝胶的快速蛋白质液相色谱(FPLC),已将可溶性合酶纯化至>90%的纯度,其比活性为5 μmol min-1 mg-1。基于聚丙烯酰胺凝胶(PlGel)色谱分析以及使用聚苯乙烯分子量标准物进行校准,PHA产物的分子量约为10(6) Da。在没有底物的情况下,合酶似乎以单体和二聚体两种形式存在。将合酶与过量底物一起温育,可将其转化为一种现在可萃取到氯仿中并在蔗糖密度超速离心时与PHA一起沉淀的形式。对底物3-D-羟基丁酰辅酶A与合酶的比例进行变化研究表明,在聚合过程中,延伸过程的发生速度比起始过程快得多。已针对聚合过程提出了一个机制模型[Griebel, R., Smith, Z., & Merrick, J. (1968) Biochemistry 7, 3676 - 3681],其中催化作用需要两个半胱氨酸。该模型基于脂肪酸生物合成中特性明确的酶。为了验证该模型,已制备了几个基于合酶之间序列保守性选择的合酶定点突变体。C459S突变体的活性约为野生型蛋白的90%,而C319S和C319A合酶的活性不到野生型蛋白的0.01%。圆二色性(CD)和抗体研究表明突变蛋白折叠正确。通过诱变仅检测到一个必需的半胱氨酸,并且在许多利用辅酶A硫酯底物的酶中,需要通过磷酸泛酰巯基乙胺进行翻译后修饰以提供第二个硫醇,这使我们考虑到合酶活性也需要翻译后修饰的可能性。当将含有PHA合酶的质粒(pKAS4)转化到需要β-丙氨酸才能生长的大肠杆菌SJ16中时,这一假设得到了证实。SJ16/pKAS4在[3H]-β-丙氨酸上生长,随后对蛋白质进行考马斯亮蓝染色和放射自显影,结果表明PHA合酶过表达,并且β-丙氨酸被掺入到蛋白质中。这些结果表明PHA合酶通过磷酸泛酰巯基乙胺进行翻译后修饰。(摘要截短至400字)