Altabe S, Iñón de Iannino N, de Mendoza D, Ugalde R A
Consejo Nacional de Investigaciones Cientificas y Technicas, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Argentina.
J Bacteriol. 1990 May;172(5):2563-7. doi: 10.1128/jb.172.5.2563-2567.1990.
Inner membranes of Azospirillum brasilense incubated with UDP-glucose were unable to synthesize beta-(1-2) glucan and lacked the 235-kilodalton intermediate protein known to be involved in the synthesis of beta-(1-2) glucan in Agrobacterium tumefaciens and Rhizobium meliloti. Inner membranes of A. brasilense strains carrying a cosmid containing the chromosomal virulence genes chvA and chvB of Agrobacterium tumefaciens formed beta-(1-2) glucan in vitro and synthesized the 235-kilodalton intermediate protein. No DNA homology to the chvB region was found in different wild-type strains of A. brasilense, but the introduction of a cosmid containing the Agrobacterium tumefaciens chvA and chvB regions yielded strains in which DNA hybridization with the chvB region was detected, provided that the strains were grown under an antibiotic selective pressure.
与UDP-葡萄糖一起孵育的巴西固氮螺菌内膜无法合成β-(1-2)葡聚糖,并且缺乏已知参与根癌土壤杆菌和苜蓿根瘤菌中β-(1-2)葡聚糖合成的235千道尔顿中间蛋白。携带含有根癌土壤杆菌染色体毒力基因chvA和chvB的黏粒的巴西固氮螺菌菌株的内膜在体外形成β-(1-2)葡聚糖并合成235千道尔顿中间蛋白。在不同的巴西固氮螺菌野生型菌株中未发现与chvB区域的DNA同源性,但引入含有根癌土壤杆菌chvA和chvB区域的黏粒后产生了能检测到与chvB区域DNA杂交的菌株,前提是这些菌株在抗生素选择压力下生长。