Tahlan Kapil, Park Hyeon Ung, Wong Annie, Beatty Perrin H, Jensen Susan E
Department of Biological Sciences, University of Alberta, Edmonton T6G 2E9, Canada.
Antimicrob Agents Chemother. 2004 Mar;48(3):930-9. doi: 10.1128/AAC.48.3.930-939.2004.
Recently, a second copy of a gene encoding proclavaminate amidinohydrolase (pah1), an enzyme involved in the early stages of clavulanic acid and clavam metabolite biosynthesis in Streptomyces clavuligerus, was identified and isolated. Using Southern analysis, we have now isolated second copies of the genes encoding the carboxyethylarginine synthase (ceaS) and beta-lactam synthetase (bls) enzymes. These new paralogues are given the gene designations ceaS1 and bls1 and are located immediately upstream of pah1 on the chromosome. Furthermore, sequence analysis of the region downstream of pah1 revealed a second copy of a gene encoding ornithine acetyltransferase (oat1), thus indicating the presence of a cluster of paralogue genes. ceaS1, bls1, and oat1 display 73, 60, and 63% identities, respectively, at the nucleotide level to the original ceaS2, bls2, and oat2 genes from the clavulanic acid gene cluster. Single mutants defective in ceaS1, bls1, or oat1 were prepared and characterized and were found to be affected to variable degrees in their ability to produce clavulanic acid and clavam metabolites. Double mutants defective in both copies of the genes were also prepared and tested. The ceaS1/ceaS2 and the bls1/bls2 mutant strains were completely blocked in clavulanic acid and clavam metabolite biosynthesis. On the other hand, oat1/oat2 double mutants still produced some clavulanic acid and clavam metabolites. This may be attributed to the presence of the argJ gene in S. clavuligerus, which encodes yet another ornithine acetyltransferase enzyme that may be able to compensate for the lack of OAT1 and -2 in the double mutants.
最近,编码原棒酸脒水解酶(pah1)的基因的第二个拷贝被鉴定并分离出来,该酶参与棒状链霉菌中棒酸和棒形代谢物生物合成的早期阶段。通过Southern分析,我们现在已经分离出了编码羧乙基精氨酸合酶(ceaS)和β-内酰胺合成酶(bls)的基因的第二个拷贝。这些新的旁系同源物被赋予基因名称ceaS1和bls1,它们位于染色体上pah1的紧邻上游。此外,对pah1下游区域的序列分析揭示了编码鸟氨酸乙酰转移酶(oat1)的基因的第二个拷贝,从而表明存在一组旁系同源基因。ceaS1、bls1和oat1在核苷酸水平上与来自棒酸基因簇的原始ceaS2、bls2和oat2基因分别具有73%、60%和63%的同一性。制备并表征了ceaS1、bls1或oat1有缺陷的单突变体,发现它们在产生棒酸和棒形代谢物的能力上受到不同程度的影响。还制备并测试了基因两个拷贝都有缺陷的双突变体。ceaS1/ceaS2和bls1/bls2突变菌株在棒酸和棒形代谢物生物合成中完全受阻。另一方面,oat1/oat2双突变体仍然产生一些棒酸和棒形代谢物。这可能归因于棒状链霉菌中存在argJ基因,该基因编码另一种鸟氨酸乙酰转移酶,它可能能够补偿双突变体中OAT1和-2的缺失。