Nakashita H, Kozuka K, Hidaka T, Hara O, Seto H
Institute of Molecular and Cellular Biosciences, The University of Tokyo, Japan.
Biochim Biophys Acta. 2000 Jan 31;1490(1-2):159-62. doi: 10.1016/s0167-4781(99)00249-3.
The first step of C-P compound biosynthesis is a C-P bond formation reaction catalyzed by phosphoenolpyruvate phosphomutase, but this reaction favors the cleavage of the C-P bond. This C-P bond forming reaction is driven by the following reaction catalyzed by phosphonopyruvate (PnPy) decarboxylase. We have cloned and sequenced the gene (bcpC) encoding PnPy decarboxylase, a key enzyme of C-P compound biosynthesis, from the bialaphos (BA) producing microorganism Streptomyces hygroscopicus by complementation methods using Streptomyces wedmorensis NP-7, which is a mutant of a fosfomycin producing strain deficient in this step. The location of this gene in the BA biosynthetic gene cluster was determined by using the expression system in Streptomyces lividans. DNA sequencing of this gene revealed a 1203-bp open reading frame encoding a polypeptide of 401 amino acids.
C-P化合物生物合成的第一步是由磷酸烯醇丙酮酸磷酸变位酶催化的C-P键形成反应,但该反应有利于C-P键的裂解。这种C-P键形成反应由磷酸丙酮酸(PnPy)脱羧酶催化的以下反应驱动。我们通过使用温德链霉菌NP-7的互补方法,从生产双丙氨膦(BA)的吸水链霉菌中克隆并测序了编码PnPy脱羧酶的基因(bcpC),PnPy脱羧酶是C-P化合物生物合成的关键酶,温德链霉菌NP-7是在这一步骤中缺陷的磷霉素生产菌株的突变体。通过使用变铅青链霉菌中的表达系统确定了该基因在BA生物合成基因簇中的位置。该基因的DNA测序揭示了一个1203 bp的开放阅读框,编码一个由401个氨基酸组成的多肽。