Sullivan John T, Brown Steven D, Yocum R Rogers, Ronson Clive W
Department of Microbiology, University of Otago, PO Box 56, Dunedin, New Zealand1.
OmniGene Bioproducts Inc., Cambridge, MA 02138, USA2.
Microbiology (Reading). 2001 May;147(Pt 5):1315-1322. doi: 10.1099/00221287-147-5-1315.
The symbiosis island of Mesorhizobium sp. strain R7A is a 500 kb chromosomal genetic element that upon transfer converts nonsymbiotic mesorhizobia to symbionts able to nodulate and fix nitrogen with Lotus corniculatus. Four genomic species of nonsymbiotic mesorhizobia have been isolated. All were auxotrophic for thiamin and biotin and three were auxotrophic for nicotinate, whereas derivatives of the strains containing the symbiosis island were prototrophic for all three vitamins. In this work, a 13.2 kb region of the island that converts the nonsymbionts to nicotinate and biotin prototrophy was characterized. The region contained orthologues of the Escherichia coli bioBFD and A genes arranged in an operon with a novel gene, bioZ, a nadABC operon, the nitrogen-fixation regulatory gene nifA, and a homologue of the pantothenate biosynthesis gene panD. The bioZ gene product was similar to beta-ketoacyl-acyl carrier protein synthase III (FabH). bioZ::Tn5 mutants grew poorly in the absence of biotin and the bioZ gene complemented an E. coli bioH mutant, suggesting that its product is involved in the synthesis of pimeloyl-COA: The bio operon was not required for symbiosis, as only mutants in the nifA gene were impaired in symbiosis, and a bioA::Tn5 mutant was not impaired in rhizosphere colonization. The rationale for the vitamin biosynthetic loci being located on an acquired genetic element that is absent from nonsymbiotic mesorhizobia remains to be determined.
中慢生根瘤菌属R7A菌株的共生岛是一个500 kb的染色体遗传元件,转移后可将非共生中慢生根瘤菌转化为能够与百脉根结瘤并固氮的共生菌。已分离出四种非共生中慢生根瘤菌基因组种。所有菌株对硫胺素和生物素均为营养缺陷型,三种对烟酸为营养缺陷型,而含有共生岛的菌株衍生物对这三种维生素均为原养型。在本研究中,对该岛上一个13.2 kb的区域进行了表征,该区域可将非共生菌转化为烟酸和生物素原养型。该区域包含大肠杆菌bioBFD和A基因的直系同源物,它们与一个新基因bioZ、一个nadABC操纵子、固氮调节基因nifA以及泛酸生物合成基因panD的一个同源物排列在一个操纵子中。bioZ基因产物与β-酮酰基-酰基载体蛋白合酶III(FabH)相似。bioZ::Tn5突变体在无生物素的情况下生长不良,bioZ基因可互补大肠杆菌bioH突变体,表明其产物参与了庚二酸单酰辅酶A的合成:共生并不需要bio操纵子,因为只有nifA基因的突变体在共生方面受损,而bioA::Tn5突变体在根际定殖方面未受损。维生素生物合成基因座位于非共生中慢生根瘤菌所没有的获得性遗传元件上的原因仍有待确定。