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担子菌齐整小核菌高效生产甘露聚糖降解酶。

Efficient production of mannan-degrading enzymes by the basidiomycete Sclerotium rolfsii.

作者信息

Sachslehner A, Haltrich D, Gübitz G, Nidetzky B, Kulbe K D

机构信息

Abteilung Biochemische Technologie, Universität für Bodenkultur BOKU (University of Agricultural Sciences, Vienna), Wien, Austria.

出版信息

Appl Biochem Biotechnol. 1998 Spring;70-72:939-53. doi: 10.1007/BF02920205.

Abstract

Sclerotium rolfsii CBS 191.62 was cultivated on a number of carbon (C) sources, including mono- and disaccharides, as well as on polysaccharides, to study the formation of different mannan-degrading enzyme activities. Highest levels of mannanase activity were obtained when alpha-cellulose-based media were used for growth, but formation of mannanase could not be enhanced by employing galactomannan as the only carbon source. Although both xylanase and cellulase formation was almost completely repressed when S. rolfsii was grown on more readily metabolizable carbohydrates, including glucose or mannose, considerable amounts of mannanase activity were secreted under these growth conditions. Enhanced mannanase production only commenced when glucose was depleted in the medium. The maximal mannanase activity of 240 IU/mL obtained in a laboratory fermentation is remarkable. Mannanase activity formed under these derepressed conditions could be mainly attributed to one major, acidic mannanase isoenzyme with a pI value of 2.75.

摘要

将齐整小核菌CBS 191.62接种在多种碳源上进行培养,这些碳源包括单糖和双糖以及多糖,以研究不同甘露聚糖降解酶活性的形成。当使用基于α-纤维素的培养基进行生长时,甘露聚糖酶活性达到最高水平,但以半乳甘露聚糖作为唯一碳源并不能增强甘露聚糖酶的形成。尽管当齐整小核菌在更易代谢的碳水化合物(包括葡萄糖或甘露糖)上生长时,木聚糖酶和纤维素酶的形成几乎完全受到抑制,但在这些生长条件下仍分泌了大量的甘露聚糖酶活性。只有当培养基中的葡萄糖耗尽时,甘露聚糖酶的产量才开始增加。在实验室发酵中获得的最大甘露聚糖酶活性为240 IU/mL,这一结果令人瞩目。在这些去阻遏条件下形成的甘露聚糖酶活性主要可归因于一种主要的酸性甘露聚糖酶同工酶,其pI值为2.75。

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