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1-Deoxy-d-Xylulose 5-Phosphate Synthase, the Gene Product of Open Reading Frame (ORF) 2816 and ORF 2895 in Rhodobacter capsulatus

机译:1-脱氧-d-木酮糖5-磷酸合酶,在荚膜红细菌中的开放阅读框(ORF)2816和ORF 2895的基因产物

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摘要

In eubacteria, green algae, and plant chloroplasts, isopentenyl diphosphate, a key intermediate in the biosynthesis of isoprenoids, is synthesized by the methylerythritol phosphate pathway. The five carbons of the basic isoprenoid unit are assembled by joining pyruvate and d-glyceraldehyde 3-phosphate. The reaction is catalyzed by the thiamine diphosphate-dependent enzyme 1-deoxy-d-xylulose 5-phosphate synthase. In Rhodobacter capsulatus, two open reading frames (ORFs) carry the genes that encode 1-deoxy-d-xylulose 5-phosphate synthase. ORF 2816 is located in the photosynthesis-related gene cluster, along with most of the genes required for synthesis of the photosynthetic machinery of the bacterium, whereas ORF 2895 is located elsewhere in the genome. The proteins encoded by ORF 2816 and ORF 2895, 1-deoxy-d-xylulose 5-phosphate synthase A and B, containing a His6 tag, were synthesized in Escherichia coli and purified to greater than 95% homogeneity in two steps. 1-Deoxy-d-xylulose 5-phosphate synthase A appears to be a homodimer with 68 kDa subunits. A new assay was developed, and the following steady-state kinetic constants were determined for 1-deoxy-d-xylulose 5-phosphate synthase A and B: Kmpyruvate = 0.61 and 3.0 mM, Kmd-glyceraldehyde 3-phosphate = 150 and 120 μM, and Vmax = 1.9 and 1.4 μmol/min/mg in 200 mM sodium citrate (pH 7.4). The ORF encoding 1-deoxy-d-xylulose 5-phosphate synthase B complemented the disrupted essential dxs gene in E. coli strain FH11.
机译:在真细菌,绿藻和植物叶绿体中,异戊二烯二磷酸(类异戊二烯生物合成的关键中间体)是通过甲基赤藓糖醇磷酸途径合成的。异戊二烯基单元的五个碳原子是通过丙酮酸和3-磷酸d-甘油醛的连接而组装的。硫胺二磷酸依赖性酶1-脱氧-d-木酮糖5-磷酸合酶催化该反应。在荚膜红细菌中,两个开放阅读框(ORF)携带编码1-脱氧-d-木酮糖5-磷酸合酶的基因。 ORF 2816与合成细菌光合作用所需的大多数基因一起位于光合作用相关的基因簇中,而ORF 2895位于基因组中的其他地方。由ORF 2816和ORF 2895编码的蛋白(含His6标签的1-脱氧-d-木酮糖5-磷酸合酶A和B)在大肠杆菌中合成,并通过两步纯化达到95%以上的同质性。 1-脱氧-d-木酮糖5-磷酸合酶A似乎是具有68kDa亚基的同型二聚体。开发了一种新的测定方法,并确定了1-脱氧-d-木酮糖5-磷酸合酶A和B的以下稳态动力学常数:丙酮酸= 0.61和3.0 mM,Kmd-甘油醛3-磷酸= 150和120μM ,在200 mM柠檬酸钠(pH 7.4)中,Vmax = 1.9和1.4μmol/ min / mg。编码1-脱氧-d-木酮糖5-磷酸合酶B的ORF补充了大肠杆菌菌株FH11中被破坏的必需dxs基因。

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