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铜绿假单胞菌脂肪酶基因的染色体定位与克隆

Chromosomal mapping and cloning of the lipase gene of Pseudomonas aeruginosa.

作者信息

Wohlfarth S, Winkler U K

机构信息

Ruhr-Universität Bochum, Lehrstuhl für Biologie der Mikroorganismen, FRG.

出版信息

J Gen Microbiol. 1988 Feb;134(2):433-40. doi: 10.1099/00221287-134-2-433.

Abstract

Various mutants (lip) of Pseudomonas aeruginosa PAO 2302 that lacked extracellular lipase activity were isolated. They were selected on a calcium-triolein agar. The phenotypic characteristics of two of these mutants suggested that they were defective in the gene coding for lipase: both lip mutants produced no lipase in liquid- and on solid medium. They were nonpleiotropic with regard to various other exoproducts. None of the mutants released any putatively cell-bound lipase after treatment of cells with Triton X-100 or alginate. The electrophoretic protein- and LPS-profiles of outer membranes derived from lip mutants and the parental strain were identical. The lip locus was mapped on the chromosome of P. aeruginosa PAO 1 by FP5- and R68. 45-mediated crossings and by transduction with phage G101. The lip locus was cotransduced with pyrF only (60%) indicating a map position at about 57 min. The lipase gene was cloned on a 3.1 kb SalI fragment using vector pKT248. The newly constructed plasmid was able to complement the lipase deficiency of the two lip mutants of P. aeruginosa.

摘要

分离出了铜绿假单胞菌PAO 2302的各种缺乏胞外脂肪酶活性的突变体(lip)。它们是在钙-三油酸甘油酯琼脂上筛选出来的。其中两个突变体的表型特征表明它们在编码脂肪酶的基因上存在缺陷:这两个lip突变体在液体培养基和固体培养基中均不产生脂肪酶。它们在其他各种胞外产物方面没有多效性。在用Triton X-100或藻酸盐处理细胞后,没有一个突变体释放出任何假定的细胞结合脂肪酶。来自lip突变体和亲本菌株的外膜的电泳蛋白质谱和脂多糖谱是相同的。通过FP5和R68.45介导的杂交以及用噬菌体G101进行转导,将lip基因座定位在铜绿假单胞菌PAO 1的染色体上。lip基因座仅与pyrF共转导(60%),表明其图谱位置约在57分钟处。使用载体pKT248将脂肪酶基因克隆在一个3.1 kb的SalI片段上。新构建的质粒能够弥补铜绿假单胞菌两个lip突变体的脂肪酶缺陷。

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