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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Comparative study of beta-glucan-degrading enzymes from Coprinopsis cinerea for their capacities to induce stipe cell wall extension
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Comparative study of beta-glucan-degrading enzymes from Coprinopsis cinerea for their capacities to induce stipe cell wall extension

机译:Coprinopsis inereaβ-葡聚糖降解酶的比较研究诱导静电细胞壁延伸的能力

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We previously reported endo-beta-1,3-glucanase ENG in combination with beta-glucosidase BGL2 at low concentration induced stipe cell wall extension. This study further explored ENG could be replaced by endo-beta-1,3(4)-glucanase ENG16A in combination with BGL2 to induce stipe cell wall extension; similarly, BGL2 could be replaced by beta-glucosidase BGL1 to cooperate with ENG to induce stipe cell wall extension. However, ENG could not be replaced by exo-beta-1,3-glucanase EXG in combination with BGL2 to induce stipe cell wall extension, although EXG alone released higher level of soluble sugars from the stipe cell walls during the reconstituted wall extension than that released from the stipe cell walls by a combination of ENG16A or ENG and BGL2 or BGL1, which was different from chitinase-mediated stipe cell wall extension. These results indicate enclo-beta-1,3-glucanases loosen the stipe cell wall, whereas exo-beta-1,3-glucanases and beta-glucosidases play a synergistic role to maintain a low and efficient concentration of endo-beta-1,3-glucanases for stipe cell wall extension. Furthermore, ENG was expressed at a very high level in the matured pilei, in contrast, ENG16A was expressed at a very high level in the elongating apical stipe. Therefore, ENG16A might be involved in stipe elongation growth, while ENG might participate in autolysis of pilei. (C) 2020 Elsevier B.V. All rights reserved.
机译:在低浓度诱导的静止细胞壁延伸,我们先前报道了Endo-Beta-1,3-葡聚糖酶ANG与β-葡糖苷酶BGL2组合。该研究进一步探索了ENG,可以由Endo-β-1,3(4)葡聚糖酶ENG16A与BGL2组合诱导诱导柄单元壁延伸;类似地,BGL2可以用β-葡糖苷酶BGL1代替,以与ENG配合以诱导静止细胞壁延伸。然而,ENGβ-1,3-葡聚糖酶EXG不能与BGL2组合代替,以诱导柄部壁延伸,尽管在重构的墙壁延伸期间EXG单独释放来自柄部壁壁的溶解糖的较高水平通过ENG16A或ENG和BGL2或BGL1的组合从柄单元壁释放,这与几丁质酶介导的静电单元壁延伸不同。这些结果表明嵌入式β-1,3-葡聚糖酶松开垫片细胞壁,而Exo-β-1,3-葡聚糖酶和β-葡糖苷酶发挥协同作用,以维持低且有效的endo-beta-1的浓度,用于静止细胞壁延伸的3葡聚糖酶。此外,ENG在成熟的李中的一个非常高的水平表示,相反,ENG16A在伸长的顶端垫片中的非常高的水平表示。因此,ENG16A可能涉及静止伸长率的增长,而ENG可能参与潜水艇的自水解。 (c)2020 Elsevier B.v.保留所有权利。

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