首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Dietary fibre degradation and fermentation by two xylanolytic bacteria Bacteroides xylanisolvens XB1AT and Roseburia intestinalis XB6B4 from the human intestine
Authors:C Mirande  E Kadlecikova  M Matulova  P Capek  A Bernalier‐Donadille  E Forano  C Béra‐Maillet
Institution:1. INRA, UR454 Unité de Microbiologie, Centre de Recherches de Clermont‐Ferrand/Theix, Saint‐Genès‐Champanelle, France;2. Institute of Chemistry, Centre for Glycomics, Slovak Academy of Sciences, Bratislava, Slovak Republic
Abstract:AimsZ: To characterize fibre degradation, colonization and fermentation, and xylanase activity of two xylanolytic bacteria Bacteroides xylanisolvens XB1AT and Roseburia intestinalis XB6B4 from the human colon. Methods and Results: The bacteria grew well on all the substrates chosen to represent dietary fibres: wheat and corn bran, pea, cabbage and leek fibres, and also on purified xylans. Roseburia intestinalis colonized the substrates more efficiently than Bact. xylanisolvens. For the two bacteria, 80–99% of the total xylanase activity was associated with the cells whatever the substrate and time of growth. Optimal specific activities of cells were obtained on oat spelt xylan; they were higher than those previously measured for xylanolytic bacteria from the human gut. Roseburia intestinalis produced high molecular mass xylanases (100–70 kDa), while Bact. xylanisolvens produced lower molecular mass enzymes, including a cell‐associated xylanase of 37 kDa. Conclusions: The two bacteria display very high xylanolytic activity on the different substrates. Differences were observed on substrate attachment and enzyme systems, suggesting that the two species occupy different niches within the gut microbiota. Significance and Impact of the Study: This study characterizes xylan degradation by two major species of the human intestine.
Keywords:Bacteroides xylanisolvens  fibre  human gut microbiota  Roseburia intestinalis  xylanase
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号