Lipeski L, Guthrie E P, O'Brien M, Kotarski S F, Salyers A A
Appl Environ Microbiol. 1986 May;51(5):978-84. doi: 10.1128/aem.51.5.978-984.1986.
Three species of colonic bacteria can ferment the mucopolysaccharide chondroitin sulfate: Bacteroides ovatus, Bacteroides sp. strain 3452A (an unnamed DNA homology group), and B. thetaiotaomicron. Proteins associated with the utilization of chondroitin sulfate by B. thetaiotaomicron have been characterized previously. In this report we compare chondroitin lyases and chondroitin sulfate-associated outer membrane polypeptides of B. ovatus and Bacteroides sp. strain 3452A with those of B. thetaiotaomicron. All three species produce two soluble cell-associated chondroitin lyases, chondroitin lyase I and II. Purified enzymes from the three species have similar pH optima, Km values, and molecular weights. However, peptide mapping experiments show that the chondroitin lyases from B. ovatus and Bacteroides sp. strain 3452A are not identical to those of B. thetaiotaomicron. A cloned gene that codes for the chondroitin lyase II from B. thetaiotaomicron hybridized on a Southern blot with DNA from B. ovatus or Bacteroides sp. strain 3452A only when low-stringency conditions were used. Antibody to chondroitin lyase II from B. thetaiotaomicron did not cross-react with chondroitin lyase II from B. ovatus or Bacteroides sp. strain 3452A. Chondroitin lyase activity in all three species was inducible by chondroitin sulfate. B. ovatus and Bacteroides sp. strain 3452A, like B. thetaiotaomicron, have outer membrane polypeptides that appear to be regulated by chondroitin sulfate, but the chondroitin sulfate-associated outer membrane polypeptides differ in molecular weight. Despite these differences, the ability of intact bacteria to utilize chondroitin sulfate, as indicated by growth yields in carbohydrate-limited continuous culture and the rate at which the chondroitin lyases were induced, was the same for all three species.
卵形拟杆菌、拟杆菌属3452A菌株(一个未命名的DNA同源群)和多形拟杆菌。此前已对多形拟杆菌利用硫酸软骨素相关的蛋白质进行了表征。在本报告中,我们将卵形拟杆菌和拟杆菌属3452A菌株的硫酸软骨素裂解酶及与硫酸软骨素相关的外膜多肽与多形拟杆菌的进行了比较。所有这三个菌种均产生两种可溶性细胞相关硫酸软骨素裂解酶,即硫酸软骨素裂解酶I和II。从这三个菌种中纯化得到的酶具有相似的最适pH值、米氏常数和分子量。然而,肽图谱实验表明,卵形拟杆菌和拟杆菌属3452A菌株的硫酸软骨素裂解酶与多形拟杆菌的并不相同。一个编码多形拟杆菌硫酸软骨素裂解酶II的克隆基因,仅在低严谨条件下,才会在Southern杂交中与卵形拟杆菌或拟杆菌属3452A菌株的DNA杂交。针对多形拟杆菌硫酸软骨素裂解酶II的抗体与卵形拟杆菌或拟杆菌属3452A菌株的硫酸软骨素裂解酶II不发生交叉反应。所有这三个菌种中的硫酸软骨素裂解酶活性均可被硫酸软骨素诱导。卵形拟杆菌和拟杆菌属3452A菌株与多形拟杆菌一样,具有似乎受硫酸软骨素调控的外膜多肽,但与硫酸软骨素相关的外膜多肽分子量不同。尽管存在这些差异,但在碳水化合物限制的连续培养中的生长产量以及硫酸软骨素裂解酶的诱导速率所表明的完整细菌利用硫酸软骨素的能力,在所有这三个菌种中是相同的。