Valentine P J, Gherardini F C, Salyers A A
Department of Microbiology, University of Illinois, Urbana 61801.
Appl Environ Microbiol. 1991 Jun;57(6):1615-23. doi: 10.1128/aem.57.6.1615-1623.1991.
An alpha-galactosidase gene has been cloned from the human colonic Bacteroides species Bacteroides ovatus 0038. This alpha-galactosidase appears to be distinct from two previously characterized alpha-galactosidases, I and II, from the same strain and has been designated alpha-galactosidase III. Partially purified alpha-galactosidase III from Escherichia coli EM24 containing pFG61 delta SE had a pI of 7.6, as compared with the reported pI values for the known alpha-galactosidases of 5.6 for I and 6.9 for II. Its molecular weight as estimated on sodium dodecyl sulfate-polyacrylamide gels was 78,000, whereas the molecular weights of alpha-galactosidases I and II were 85,000 and 80,500, respectively. The only substrate hydrolyzed by alpha-galactosidase III was melibiose, whereas the other two alpha-galactosidases were able to degrade melibiose, raffinose, and stachyose and partially degraded guar gum. alpha-Galactosidase III had a pH optimum of 6.7 to 7.2. Finally, a single crossover insertion which disrupted the gene in the B. ovatus chromosome had no effect on expression of alpha-galactosidases I and II. Although this insertion had no effect on the ability of B. ovatus to grow in laboratory medium on any of the galactoside-containing carbohydrates tested, the insertion mutant was outcompeted by wild type when a combination of mutant and wild type was used to colonize germfree mice. Insertions on either side of the gene had the same effect. Thus, the locus which contains alpha-galactosidase III may be important for colonization in vivo.(ABSTRACT TRUNCATED AT 250 WORDS)
已从人结肠拟杆菌属物种卵形拟杆菌0038中克隆出一个α-半乳糖苷酶基因。这种α-半乳糖苷酶似乎与同一菌株中先前鉴定的两种α-半乳糖苷酶I和II不同,被命名为α-半乳糖苷酶III。从含有pFG61δSE的大肠杆菌EM24中部分纯化的α-半乳糖苷酶III的等电点为7.6,而已知α-半乳糖苷酶I的等电点报道为5.6,II为6.9。在十二烷基硫酸钠-聚丙烯酰胺凝胶上估计其分子量为78,000,而α-半乳糖苷酶I和II的分子量分别为85,000和80,500。α-半乳糖苷酶III唯一水解的底物是蜜二糖,而其他两种α-半乳糖苷酶能够降解蜜二糖、棉子糖和水苏糖,并部分降解瓜尔胶。α-半乳糖苷酶III的最适pH为6.7至7.2。最后,在卵形拟杆菌染色体中破坏该基因的单交换插入对α-半乳糖苷酶I和II的表达没有影响。尽管这种插入对卵形拟杆菌在实验室培养基中在所测试的任何含半乳糖苷的碳水化合物上生长的能力没有影响,但当使用突变体和野生型的组合来定殖无菌小鼠时,插入突变体被野生型淘汰。基因两侧的插入具有相同的效果。因此,含有α-半乳糖苷酶III的基因座可能对体内定殖很重要。(摘要截断于250字)