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首页> 外文期刊>Applied and Environmental Microbiology >Importance of mucopolysaccharides as substrates for Bacteroides thetaiotaomicron growing in intestinal tracts of exgermfree mice.
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Importance of mucopolysaccharides as substrates for Bacteroides thetaiotaomicron growing in intestinal tracts of exgermfree mice.

机译:黏多糖作为无细菌小鼠肠道中生长的拟杆菌的底物的重要性。

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摘要

We used two approaches to determine whether the mucopolysaccharide chondroitin sulfate is an important source of carbon and energy for Bacteroides thetaiotaomicron in the intestinal tracts of germfree mice. First, we tested the ability of three mutants that grew poorly or not at all on chondroitin sulfate to colonize the intestinal tract of a germfree mouse and to compete with wild-type B. thetaiotaomicron in this model system. One mutant (CG10) was rapidly outcompeted by the wild type. However, since this mutant was unable to grow on chondroitin sulfate because it could not grow on N-acetyl-galactosamine, one of its monosaccharide components, this mutant might also be unable to utilize glycoprotein mucins. Two mutants (46-1 and 46-4) were isolated that grew poorly on chondroitin sulfate but normally on both component sugars. One of them was outcompeted by the wild type, but the percent wild type increased more slowly than with CG10. In one experiment, the percent wild type never reached 100%. The other (46-4) was not outcompeted by the wild type. These results indicate that, although chondroitin sulfate may be a carbon source in the animal, it is not of major importance. Our second approach was to determine by immunoblot analysis whether a 28-kilodalton outer membrane protein that is produced by B. thetaiotaomicron only when it is grown on chondroitin sulfate or hyaluronic acid was being produced at induced level by B. thetaiotaomicron growing in the ceca of exgermfree mice. There was no evidence for induction of this protein in vivo. Thus, the immunoblot results are consistent with results of the mutant competition experiments.
机译:我们使用两种方法来确定粘多糖硫酸软骨素是否是无菌小鼠肠道中拟杆菌(Bacteroides thetaiotaomicron)的碳和能量的重要来源。首先,我们测试了在硫酸软骨素上生长不佳或根本没有生长的三个突变体在此模型系统中定植于无菌小鼠肠道中并与野生型B. thetaiotaomicron竞争的能力。一种突变体(CG10)被野生型迅速竞争。然而,由于该突变体不能在硫酸软骨素上生长,因为它不能在其单糖成分之一的N-乙酰基-半乳糖胺上生长,因此该突变体也可能无法利用糖蛋白粘蛋白。分离出两个突变体(46-1和46-4),它们在硫酸软骨素上生长较差,但在两种糖上均正常生长。其中之一在野生型方面胜过竞争,但野生型百分比的增长速度比CG10慢。在一个实验中,野生型百分比从未达到100%。另一个(46-4)没有被野生型竞争。这些结果表明,尽管硫酸软骨素可能是动物中的碳源,但并不是很重要。我们的第二种方法是通过免疫印迹分析来确定仅在硫酸软骨素或透明质酸上生长时,由泰氏芽孢杆菌产生的28千达尔顿外膜蛋白是否由在大肠杆菌中生长的B. thetaiotaomicron诱导水平产生。无胚小鼠。没有证据可以在体内诱导这种蛋白质。因此,免疫印迹结果与突变竞争实验的结果一致。

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