Okada K, Kainou T, Tanaka K, Nakagawa T, Matsuda H, Kawamukai M
Department of Applied Bioscience and Biotechnology, Faculty of Life and Environmental Science, Nishikawatsu, Matsue, Japan.
Eur J Biochem. 1998 Jul 1;255(1):52-9. doi: 10.1046/j.1432-1327.1998.2550052.x.
Decaprenyl diphosphate (decaprenyl-PP) synthase catalyzes the consecutive condensation of isopentenyl diphosphate with allylic diphosphates to produce decaprenyl-PP, which is used for the side chain of ubiquinone (Q)-10. We have cloned the synthase gene, designated ddsA, from Gluconobacter suboxydans and expressed it in Escherichia coli. Sequence analysis revealed the presence of an ORF of 948 bp capable of encoding a 33,898-Da polypeptide that displays high similarity (30-50%) to other prenyl diphosphate synthases. Expression of the ddsA gene complemented the lethality resulting from a defect in the octaprenyl diphosphate synthase gene of E. coli and produced Q-10, indicating that Q-10 can substitute for the function of Q-8. The His-tagged DdsA protein was purified to characterize its enzymatic properties. This enzyme required detergent (0.05% Triton X-100) and 10 mM Mg2+, for full activity. The Michaelis constants for geranyl diphosphate, all-E-farnesyl diphosphate and all-E-geranylgeranyl diphosphate were 7.00, 0.50 and 0.32 microM, respectively. Nine single-amino-acid substitutions were introduced upstream of conserved region II or VI. Most of the mutants showed a considerable decrease in catalytic activity or shortening of the ultimate chain length. However, the A70G mutant produced a longer-chain-length product than wild-type decaprenyl-PP synthase, and the A70Y mutant completely abolished the decaprenyl-PP synthase function, indicating that Ala70 is important for enzyme activity and the determination of the chain-length properties of DdsA.
癸异戊二烯基二磷酸合酶催化异戊烯基二磷酸与烯丙基二磷酸的连续缩合反应,生成癸异戊二烯基二磷酸,该产物用于泛醌(Q)-10的侧链合成。我们已经从氧化葡萄糖杆菌中克隆了该合酶基因,命名为ddsA,并在大肠杆菌中进行了表达。序列分析显示存在一个948 bp的开放阅读框,能够编码一个33898 Da的多肽,该多肽与其他异戊二烯基二磷酸合酶具有高度相似性(30 - 50%)。ddsA基因的表达弥补了大肠杆菌八异戊二烯基二磷酸合酶基因缺陷导致的致死性,并产生了Q-10,这表明Q-10可以替代Q-8的功能。带有组氨酸标签的DdsA蛋白被纯化以表征其酶学性质。该酶需要去污剂(0.05% Triton X-100)和10 mM Mg2+才能达到完全活性。香叶基二磷酸、全-E-法尼基二磷酸和全-E-香叶基香叶基二磷酸的米氏常数分别为7.00、0.50和0.32 microM。在保守区域II或VI的上游引入了9个单氨基酸替换。大多数突变体的催化活性显著降低或最终链长缩短。然而,A70G突变体产生的产物链长比野生型癸异戊二烯基二磷酸合酶更长,而A70Y突变体完全消除了癸异戊二烯基二磷酸合酶的功能,这表明丙氨酸70对于酶活性和DdsA链长性质的确定很重要。