首页> 外文OA文献 >Isolation and characterization of Bacillus subtilis genes involved in siderophore biosynthesis: relationship between B. subtilis sfpo and Escherichia coli entD genes.
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Isolation and characterization of Bacillus subtilis genes involved in siderophore biosynthesis: relationship between B. subtilis sfpo and Escherichia coli entD genes.

机译:枯草芽孢杆菌生物合成中涉及的枯草芽孢杆菌基因的分离和鉴定:枯草芽孢杆菌sfpo与大肠杆菌entD基因之间的关系。

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摘要

In response to iron deprivation, Bacillus subtilis secretes a catecholic siderophore, 2,3-dihydroxybenzoyl glycine, which is similar to the precursor of the Escherichia coli siderophore enterobactin. We isolated two sets of B. subtilis DNA sequences that complemented the mutations of several E. coli siderophore-deficient (ent) mutants with defective enterobactin biosynthesis enzymes. One set contained DNA sequences that complemented only an entD mutation. The second set contained DNA sequences that complemented various combinations of entB, entE, entC, and entA mutations. The two sets of DNA sequences did not appear to overlap. AB. subtilis mutant containing an insertion in the region of the entD homolog grew much more poorly in low-iron medium and with markedly different kinetics. These data indicate that (i) at least five of the siderophore biosynthesis genes of B. subtilis can function in E. coli, (ii) the genetic organization of these siderophore genes in B. subtilis is similar to that in E. coli, and (iii) the B. subtilis entD homolog is required for efficient growth in low-iron medium. The nucleotide sequence of the B. subtilis DNA contained in plasmid pENTA22, a clone expressing the B. subtilis entD homolog, revealed the presence of at least two genes. One gene was identified as sfpo, a previously reported gene involved in the production of surfactin in B. subtilis and which is highly homologous to the E. coli entD gene. We present evidence that the E. coli entD and B. subtilis sfpo genes are interchangeable and that their products are members of a new family of proteins which function in the secretion of peptide molecules.
机译:响应铁缺乏,枯草芽孢杆菌分泌一种儿茶酚铁载体2,3-二羟基苯甲酰基甘氨酸,与大肠杆菌铁载体肠杆菌素的前体相似。我们分离了两组枯草芽孢杆菌DNA序列,它们补充了具有缺陷的肠杆菌素生物合成酶的几个大肠杆菌铁载体缺陷(ent)突变体的突变。一组包含仅补充entD突变的DNA序列。第二组包含互补entB,entE,entC和entA突变的各种组合的DNA序列。两组DNA序列似乎没有重叠。 AB。在低铁培养基中,在entD同源物区域内含有插入片段的枯草芽孢杆菌突变体生长较差,并且动力学显着不同。这些数据表明:(i)枯草芽孢杆菌的至少5个铁载体生物合成基因可以在大肠杆菌中起作用;(ii)枯草芽孢杆菌中这些铁载体基因的遗传组织与大肠杆菌相似,并且(iii)在低铁培养基中有效生长需要枯草芽孢杆菌entD同源物。表达枯草芽孢杆菌entD同源物的质粒pENTA22中所含的枯草芽孢杆菌DNA的核苷酸序列揭示了至少两个基因的存在。一个基因被鉴定为sfpo,这是先前报道的与枯草芽孢杆菌中表面活性素产生有关的基因,与大肠杆菌entD基因高度同源。我们目前的证据表明,大肠杆菌entD和枯草芽孢杆菌sfpo基因是可互换的,并且它们的产物是在肽分子分泌中起作用的新蛋白质家族的成员。

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