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来自豌豆根瘤菌蚕豆生物型的脲酶基因簇的特性分析。

Characterization of the urease gene cluster from Rhizobium leguminosarum bv. viciae.

作者信息

Toffanin Annita, Cadahia Esther, Imperial Juan, Ruiz-Argüeso Tomás, Palacios Manuel

机构信息

Departmento de Biotecnología, Escuela Técnica Superior de Ingenieros Agrónomos, Universidad Politécnica de Madrid, Ciudad Universitaria s/n, Spain.

出版信息

Arch Microbiol. 2002 Apr;177(4):290-8. doi: 10.1007/s00203-001-0392-0. Epub 2002 Jan 31.

Abstract

Moderate levels of urease activity (ca. 300 mU mg(-1)) were detected in Rhizobium leguminosarum bv. viciae UPM791 vegetative cells. This activity did not require urea for induction and was partially repressed by the addition of ammonium into the medium. Lower levels of urease activity (ca. 100 mU mg(-1)) were detected also in pea bacteroids. A DNA region of ca. 9 kb containing the urease structural genes ( ureA, ureB and ureC), accessory genes ( ureD, ureE, ureF, and ureG), and five additional ORFs ( orf83, orf135, orf207, orf223, and orf287) encoding proteins of unknown function was sequenced. Three of these ORFs ( orf83, orf135 and orf207) have a homologous counterpart in a gene cluster from Sinorhizobium meliloti, reported to be involved in urease and hydrogenase activities. R. leguminosarum mutant strains carrying Tn 5 insertions within this region exhibited a urease-negative phenotype, but induced wild-type levels of hydrogenase and nitrogenase activities in bacteroids. orf287 encodes a potential transmembrane protein with a C-terminal GGDEF domain. A mutant affected in orf287 exhibited normal levels of urease activity in culture cells. Experiments aimed at cross-complementing Ni-binding proteins required for urease and hydrogenase synthesis (UreE and HypB, respectively) indicated that these two proteins are not functionally interchangeable in R. leguminosarum.

摘要

在豌豆根瘤菌蚕豆生物型UPM791的营养细胞中检测到中等水平的脲酶活性(约300 mU mg⁻¹)。该活性不需要尿素诱导,并且通过向培养基中添加铵而部分受到抑制。在豌豆类菌体中也检测到较低水平的脲酶活性(约100 mU mg⁻¹)。对一个约9 kb的DNA区域进行了测序,该区域包含脲酶结构基因(ureA、ureB和ureC)、辅助基因(ureD、ureE、ureF和ureG)以及另外五个编码功能未知蛋白质的开放阅读框(orf83、orf135、orf207、orf223和orf287)。这些开放阅读框中的三个(orf83、orf135和orf207)在苜蓿中华根瘤菌的一个基因簇中有同源对应物,据报道该基因簇与脲酶和氢化酶活性有关。在该区域内携带Tn5插入的豌豆根瘤菌突变菌株表现出脲酶阴性表型,但在类菌体中诱导出野生型水平的氢化酶和固氮酶活性。orf287编码一种具有C端GGDEF结构域的潜在跨膜蛋白。一个受orf287影响的突变体在培养细胞中表现出正常水平的脲酶活性。旨在对脲酶和氢化酶合成所需的镍结合蛋白(分别为UreE和HypB)进行交叉互补的实验表明,这两种蛋白在豌豆根瘤菌中功能上不可互换。

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