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首页> 外文期刊>Biochimica et Biophysica Acta. Protein Structure and Molecular Enzymology >Endoglucanase activity and relative expression of glycoside hydrolase genes of Fibrobacter succinogenes S85 grown on different substrates
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Endoglucanase activity and relative expression of glycoside hydrolase genes of Fibrobacter succinogenes S85 grown on different substrates

机译:生长在不同底物上的琥珀酸根瘤菌S85的内切葡聚糖酶活性和糖苷水解酶基因的相对表达

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摘要

The endoglucanase activity of cells and extracellular culture fluid of Fibrobacter succinogenes S85 grown on glucose, cellobiose, soluble polysaccharides (β-glucan, lichenan) and intact plant polysaccharides, was compared. The specific activity of cells grown on cellulose or forages was 6- to 20-fold higher than that of cells grown on soluble substrates, suggesting an induction of endoglucanases by the insoluble substrates. The ratios of cells to extracellular culture fluid endoglucanase activities measured in cultures grown on sugars or insoluble polysaccharides suggested that the endoglucanases induced by the insoluble polysaccharides remained attached to the cells. The mRNA of all the F. succinogenes glycoside hydrolase genes sequenced so far were then quantified in cells grown on glucose, cellobiose or cellulose. The results show that all these genes were transcribed in growing cells, and that they are all overexpressed in cultures grown on cellulose. Endoglucanase-encoding endB and endA_(FS) genes, and xylanase-encoding xynC gene appeared the most expressed genes in growing cells. EGB and ENDA are thus likely to play a major role in cellulose degradation in F. succinogenes.
机译:比较了在葡萄糖,纤维二糖,可溶性多糖(β-葡聚糖,地衣聚糖)和完整植物多糖上生长的琥珀酸根瘤菌S85细胞和胞外培养液的内切葡聚糖酶活性。在纤维素或牧草上生长的细胞的比活性比在可溶性底物上生长的细胞高6至20倍,表明不溶性底物可诱导内切葡聚糖酶。在糖或不溶性多糖上培养的培养物中测得的细胞与细胞外培养液内切葡聚糖酶活性的比率表明,由不溶性多糖诱导的内切葡聚糖酶保持附着在细胞上。然后,对在葡萄糖,纤维二糖或纤维素上生长的细胞中迄今已测序的所有琥珀酸葡萄球菌糖苷水解酶基因的mRNA进行定量。结果表明,所有这些基因都在生长的细胞中转录,并且它们在纤维素生长的培养物中均过表达。编码内切葡聚糖酶的endB和endA_(FS)基因以及编码木聚糖酶的xynC基因在生长中的细胞中表达最多。因此,EGB和ENDA可能在琥珀酸杆菌的纤维素降解中起主要作用。

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