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一种在共生铁获取方面存在缺陷的豌豆根瘤菌突变体。

A Rhizobium leguminosarum mutant defective in symbiotic iron acquisition.

作者信息

Nadler K D, Johnston A W, Chen J W, John T R

机构信息

Department of Botany and Plant Pathology, Michigan State University, East Lansing 48824.

出版信息

J Bacteriol. 1990 Feb;172(2):670-7. doi: 10.1128/jb.172.2.670-677.1990.

Abstract

Iron acquisition by symbiotic Rhizobium spp. is essential for nitrogen fixation in the legume root nodule symbiosis. Rhizobium leguminosarum 116, an ineffective mutant strain with a defect in iron acquisition, was isolated after nitrosoguanidine mutagenesis of the effective strain 1062. The pop-1 mutation in strain 116 imparted to it a complex phenotype, characteristic of iron deficiency: the accumulation of porphyrins (precursors of hemes) so that colonies emitted a characteristic pinkish-red fluorescence when excited by UV light, reduced levels of cytochromes b and c, and wild-type growth on high-iron media but low or no growth in low-iron broth and on solid media supplemented with the iron scavenger dipyridyl. Several iron(III)-solubilizing agents, such as citrate, hydroxyquinoline, and dihydroxybenzoate, stimulated growth of 116 on low-iron solid medium; anthranilic acid, the R. leguminosarum siderophore, inhibited low-iron growth of 116. The initial rate of 55Fe uptake by suspensions of iron-starved 116 cells was 10-fold less than that of iron-starved wild-type cells. Electron microscopic observations revealed no morphological abnormalities in the small, white nodules induced by 116. Nodule cortical cells were filled with vesicles containing apparently normal bacteroids. No premature degeneration of bacteroids or of plant cell organelles was evident. We mapped pop-1 by R plasmid-mediated conjugation and recombination to the ade-27-rib-2 region of the R. leguminosarum chromosome. No segregation of pop-1 and the symbiotic defect was observed among the recombinants from these crosses. Cosmid pKN1, a pLAFR1 derivative containing a 24-kilobase-pair fragment of R. leguminosarum DNA, conferred on 116 the ability to grow on dipyridyl medium and to fix nitrogen symbiotically. These results indicate that the insert cloned in pKN1 encodes an element of the iron acquisition system of R. leguminosarum that is essential for symbiotic nitrogen fixation.

摘要

共生根瘤菌获取铁元素对于豆科植物根瘤共生固氮至关重要。豌豆根瘤菌116是一株在铁获取方面存在缺陷的无效突变菌株,它是由有效菌株1062经亚硝基胍诱变后分离得到的。菌株116中的pop - 1突变赋予其一种复杂的表型,这是缺铁的特征:卟啉(血红素的前体)积累,使得菌落在紫外光激发下发出特征性的粉红色荧光,细胞色素b和c水平降低,在高铁培养基上生长表现为野生型,但在低铁肉汤以及添加铁螯合剂联吡啶的固体培养基上生长缓慢或不生长。几种铁(III)增溶剂,如柠檬酸盐、羟基喹啉和二羟基苯甲酸盐,可刺激116在低铁固体培养基上生长;邻氨基苯甲酸,即豌豆根瘤菌的铁载体,抑制116在低铁条件下的生长。缺铁的116细胞悬液对55Fe的初始摄取速率比缺铁的野生型细胞低10倍。电子显微镜观察显示,116诱导形成的小的白色根瘤没有形态异常。根瘤皮层细胞充满了含有明显正常类菌体的小泡。未观察到类菌体或植物细胞器过早退化。我们通过R质粒介导的接合和重组将pop - 1定位到豌豆根瘤菌染色体的ade - 27 - rib - 2区域。在这些杂交产生的重组体中未观察到pop - 1与共生缺陷的分离。黏粒pKN1是一种pLAFR1衍生物,含有一段24千碱基对的豌豆根瘤菌DNA片段,赋予116在联吡啶培养基上生长并进行共生固氮的能力。这些结果表明,克隆到pKN1中的插入片段编码豌豆根瘤菌铁获取系统的一个元件,该元件对于共生固氮至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a34d/208491/9f54d194685f/jbacter01044-0172-a.jpg

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