Hara O, Anzai H, Imai S, Kumada Y, Murakami T, Itoh R, Takano E, Satoh A, Nagaoka K
Pharmaceutical Research Laboratories, Meiji Seika Kaisha, Ltd., Yokohama, Japan.
J Antibiot (Tokyo). 1988 Apr;41(4):538-47. doi: 10.7164/antibiotics.41.538.
We have isolated and studied the genes involved in the alanylation step in the biosynthesis of a herbicide, bialaphos which is produced by Streptomyces hygroscopicus. Three bialaphos-nonproducing mutants, NP60, NP61 and NP62, isolated from S. hygroscopicus by treatment with N-methyl-N'-nitro-N-nitrosoguanidine were defective for the alanylation step and were not restored to productivity by any locus of the gene cluster previously cloned. Three plasmids were isolated using NP60, NP61 and NP62 as recipients. The genes which restored productivity to NP61 and NP62 hybridized to the contiguous region of the bialaphos biosynthetic gene cluster. The gene cluster involved in the bialaphos production was about 35 kb long. The gene which restored productivity to NP60 did not hybridize to the bialaphos biosynthetic gene cluster. VM3 and VM4, putative alanylation blocked mutants, were derived from a bialaphos producer by gene replacement of an unidentified region of the biosynthetic gene cluster with an in vitro altered DNA sequence. The genes which restored productivity to VM3 and VM4 were located between the genes which code for phosphinomethylmalic acid synthase and demethylphosphinothricin acetyltransferase in the cluster. These results suggest that multiple genes are involved in the alanylation step.
我们已经分离并研究了参与除草剂双丙氨膦生物合成丙氨酰化步骤的基因,双丙氨膦由吸水链霉菌产生。通过用N-甲基-N'-硝基-N-亚硝基胍处理从吸水链霉菌中分离出三个不产生双丙氨膦的突变体NP60、NP61和NP62,它们在丙氨酰化步骤中存在缺陷,并且先前克隆的基因簇的任何位点都不能恢复其生产能力。以NP60、NP61和NP62为受体分离出三个质粒。使NP61和NP62恢复生产能力的基因与双丙氨膦生物合成基因簇的相邻区域杂交。参与双丙氨膦生产的基因簇约35kb长。使NP60恢复生产能力的基因与双丙氨膦生物合成基因簇不杂交。VM3和VM4是假定的丙氨酰化受阻突变体,通过用体外改变的DNA序列替换生物合成基因簇的一个未鉴定区域,从双丙氨膦生产者中获得。使VM3和VM4恢复生产能力的基因位于该簇中编码膦酰基甲基苹果酸合酶和脱甲基膦丝菌素乙酰转移酶的基因之间。这些结果表明,丙氨酰化步骤涉及多个基因。