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首页> 外文期刊>Journal of applied microbiology >UTILIZATION OF STARCH AND SYNTHESIS OF A COMBINED AMYLASE/ALPHA-GLUCOSIDASE BY THE HUMAN COLONIC ANAEROBE BACTEROIDES OVATUS
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UTILIZATION OF STARCH AND SYNTHESIS OF A COMBINED AMYLASE/ALPHA-GLUCOSIDASE BY THE HUMAN COLONIC ANAEROBE BACTEROIDES OVATUS

机译:人类结肠厌氧杆菌卵的淀粉利用及淀粉酶/α-葡糖苷酶的合成

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摘要

Bacteroides ovatus preferentially utilized starch and pectin when grown on a mixture of polysaccharides in batch culture, indicating that these carbohydrates are important substrates for the bacterium in the human large intestine. Further studies on starch breakdown showed that continuous cultures grew on the polysaccharide when it provided the sole carbohydrate source, to yield a single hydrolytic product at low dilution rates (D = 0.04 h(-1)), with an estimated molecular mass of 13 kDa. In contrast, two major types of oligomeric products were formed at higher dilution rates (D = 0.44 h(-1)), with approximate molecular weights of 11 and 140 kDa. Analysis of cell-associated starch-degrading enzymes produced by Bact. ovatus using ion exchange chromatography and HPLC gel-filtration showed that amylase and alpha-glucosidase activities eluted in the same fractions. The single peak containing amylase and alpha-glucosidase activities obtained by HPLC gel-filtration chromatography corresponded to a molecular mass of approximately 140 kDa, and activity staining of gels for alpha-glucosidase activity after polyacrylamide gel electrophoresis, in the presence of sodium dodecyl sulphate, gave an estimated molecular mass of 70 kDa, indicating this enzyme to be a dimer. After renaturation, the 70 kDa band was cut from the gels and solubilized. The extract hydrolysed gelatinized starch and p-nitrophenyl-alpha-D-glucopyranoside.
机译:当在分批培养中的多糖混合物上生长时,卵形拟杆菌优选利用淀粉和果胶,这表明这些碳水化合物是人大肠中细菌的重要底物。对淀粉分解的进一步研究表明,当多糖提供唯一的碳水化合物来源时,连续培养物就在多糖上生长,从而以低稀释率(D = 0.04 h(-1))产生单一的水解产物,估计分子量为13 kDa 。相反,两种主要类型的寡聚产物以较高的稀释率(D = 0.44 h(-1))形成,分子量约为11和140 kDa。 Bact产生的细胞相关淀粉降解酶的分析。使用离子交换色谱和HPLC凝胶过滤法对卵巢进行分析,结果表明淀粉酶和α-葡萄糖苷酶的活性被洗脱在相同的馏分中。通过HPLC凝胶过滤色谱获得的含有淀粉酶和α-葡萄糖苷酶活性的单个峰对应于约140 kDa的分子量,并且在聚丙烯酰胺凝胶电泳后在十二烷基硫酸钠存在下,凝胶对α-葡萄糖苷酶活性的凝胶染色估计分子量为70 kDa,表明该酶是二聚体。复性后,从凝胶上切下70 kDa条带并溶解。提取物水解糊化淀粉和对硝基苯基-α-D-吡喃葡萄糖苷。

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