首页> 美国卫生研究院文献>Biochemical Journal >Study of the mode of action and site-specificity of the endo-(1----4)-beta-D-glucanases of the fungus Penicillium pinophilum with normal 1-3H-labelled reduced and chromogenic cello-oligosaccharides.
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Study of the mode of action and site-specificity of the endo-(1----4)-beta-D-glucanases of the fungus Penicillium pinophilum with normal 1-3H-labelled reduced and chromogenic cello-oligosaccharides.

机译:带有正常的1-3H标记的还原的和发色的纤维寡糖的真菌青霉菌内-(1 ---- 4)-β-D-葡聚糖酶的作用方式和位点特异性的研究。

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摘要

The modes of action of the five major endo-(1----4)-beta-D-glucanases (I, II, III, IV and V) purified from Penicillium pinophilum cellulase were compared by h.p.l.c. analysis, with normal, 1-3H-labelled and reduced cello-oligosaccharides and 4-methylumbelliferyl glycosides as substrates. Significant differences were observed in the preferred site of cleavage even when substrates with the same number of glycosidic bonds were compared. Thus, although endoglucanase I was unable to attack normal cello-oligosaccharides shorter than degree of polymerization 6, it hydrolysed reduced cellopentaose to yield cellotriose and cellobi-itol, and it produced cellotriose and 4-methylumbelliferyl glucoside from 4-methylumbelliferyl cellotetraoside. Endoglucanase IV hydrolysed [1-3H]cellotriose but did not attack either cellotri-itol or 4-methylumbelliferyl cellobioside. These and other anomalous results indicated clearly that modification of the reducing glycosyl residue on the cello-oligosaccharides induces in an apparent change in the mode of action of the endoglucanases. It is suggested that, although cello-oligosaccharide derivatives are useful for differentiating and classifying endoglucanases, conclusions on the mechanism of cellulase action resulting from these measurements should be treated cautiously. Unequivocal information on the mode of endoglucanase action on cello-oligosaccharides was obtained with radiolabelled cello-oligosaccharides of degree of polymerization 3 to 5. Indications that transglycosylation was a property of the endoglucanases were particularly evident with the 4-methylumbelliferyl cello-oligosaccharides. Turnover numbers for hydrolysis of the umbelliferyl cello-oligosaccharides were calculated, and these, along with the other analytical data collected on the products of hydrolysis of the normal, reduced and radiolabelled cello-oligosaccharides, suggested that the various endoglucanases had different roles to play in the overall hydrolysis of cellulose to sugars small enough to be transported through the cell membrane.
机译:通过h.p.l.c比较了从嗜绿青霉纤维素酶中纯化的5种主要的内-(1-4)-β-D-葡聚糖酶(I,II,III,IV和V)的作用方式。用正常的1-3H标记和还原的纤维寡糖和4-甲基伞形糖苷作为底物进行分析。即使比较具有相同糖苷键数目的底物,在优选的切割位点也观察到显着差异。因此,尽管内切葡聚糖酶I不能短于聚合度6来攻击正常的纤维寡糖,但是它水解还原的纤维戊糖产生纤维三糖和纤维二糖醇,并且从4-甲基伞形基纤维四糖苷产生纤维素三糖和4-甲基伞形基葡萄糖苷。内切葡聚糖酶IV水解[1-3H]纤维三糖,但不攻击纤维三糖醇或4-甲基伞形基纤维二糖苷。这些和其他异常结果清楚地表明,纤维寡糖上的还原性糖基残基的修饰引起内切葡聚糖酶的作用方式的明显变化。有人建议,尽管纤维寡糖衍生物可用于区分和分类内切葡聚糖酶,但应谨慎对待由这些测量结果产生的纤维素酶作用机理的结论。用聚合度为3到5的放射性标记的纤维寡糖获得了有关内切葡聚糖酶对纤维寡糖作用方式的明确信息。使用4-甲基伞形基纤维寡糖特别表明,转糖基化是内切葡聚糖酶的特性。计算了伞形基纤维寡糖水解的周转数,这些数据以及收集的有关正常,还原和放射性标记的纤维寡糖水解产物的其他分析数据表明,各种内切葡聚糖酶在其中的作用不同。纤维素水解成糖的总水解量要小到足以通过细胞膜转运。

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