Ugalde R A, Coira J A, Brill W J
J Bacteriol. 1986 Oct;168(1):270-5. doi: 10.1128/jb.168.1.270-275.1986.
Previous work showed that two different strains derived from a culture of Rhizobium meliloti 102F51 differed with respect to phage specificity, agglutinability by alfalfa seed lectin, and synthesis of a galactose-containing polysaccharide (R. A. Ugalde, H. Handelsman, and W. J. Brill, J. Bacteriol. 166:148-154, 1986). Inner membranes from the more competitive strain incorporated galactose from UDP-galactose when a thermostable factor was present. This factor has now been identified as UDP-galacturonic acid. UDP-glucuronic acid was also active as a donor; however, this activity may be due to the presence of a 4-epimerase. Galacturonic acid, together with galactose, is incorporated into the reaction product, which appears to be a polysaccharide formed by several repeating units of these two monosaccharides. Partial acid hydrolysis liberates the disaccharide with galactose at the reducing end.
先前的研究表明,源自苜蓿中华根瘤菌102F51培养物的两种不同菌株在噬菌体特异性、苜蓿种子凝集素的凝集性以及含半乳糖多糖的合成方面存在差异(R. A. 乌加尔德、H. 汉德尔斯曼和W. J. 布里尔,《细菌学杂志》166:148 - 154,1986年)。当存在一种热稳定因子时,更具竞争力的菌株的内膜会从UDP - 半乳糖中掺入半乳糖。现在已确定该因子为UDP - 半乳糖醛酸。UDP - 葡萄糖醛酸作为供体也具有活性;然而,这种活性可能归因于4 - 表异构酶的存在。半乳糖醛酸与半乳糖一起被掺入反应产物中,该反应产物似乎是由这两种单糖的几个重复单元形成的多糖。部分酸水解会释放出还原端带有半乳糖的二糖。