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微生物木聚糖酶:工程、生产及工业应用。

Microbial xylanases: engineering, production and industrial applications.

机构信息

Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research (A*STAR), 1 Pesek Road, Jurong Island, Singapore 627833, Singapore.

出版信息

Biotechnol Adv. 2012 Nov-Dec;30(6):1219-27. doi: 10.1016/j.biotechadv.2011.11.006. Epub 2011 Nov 25.

Abstract

Enzymatic depolymerization of hemicellulose to monomer sugars needs the synergistic action of multiple enzymes, among them endo-xylanases (EC 3.2.1.8) and β-xylosidases (EC 3.2.1.37) (collectively xylanases) play a vital role in depolymerizing xylan, the major component of hemicellulose. Recent developments in recombinant protein engineering have paved the way for engineering and expressing xylanases in both heterologous and homologous hosts. Functional expression of endo-xylanases has been successful in many hosts including bacteria, yeasts, fungi and plants with yeasts being the most promising expression systems. Functional expression of β-xylosidases is more challenging possibly due to their more complicated structures. The structures of endo-xylanases of glycoside hydrolase families 10 and 11 have been well elucidated. Family F/10 endo-xylanases are composed of a cellulose-binding domain and a catalytic domain connected by a linker peptide with a (β/α)8 fold TIM barrel. Family G/11 endo-xylanases have a β-jelly roll structure and are thought to be able to pass through the pores of hemicellulose network owing to their smaller molecular sizes. The structure of a β-D-xylosidase belonging to family 39 glycoside hydrolase has been elucidated as a tetramer with each monomer being composed of three distinct regions: a catalytic domain of the canonical (β/α)8--TIM barrel fold, a β-sandwich domain and a small α-helical domain with the enzyme active site that binds to D-xylooligomers being present on the upper side of the barrel. Glycosylation is generally considered as one of the most important post-translational modifications of xylanases, but a few examples showed functional expression of eukaryotic xylanases in bacteria. The optimal ratio of these synergistic enzymes is very important in improving hydrolysis efficiency and reducing enzyme dosage but has hardly been addressed in literature. Xylanases have been used in traditional fields such as food, feed and paper industries for a longer time but more and more attention has been paid to using them in producing sugars and other chemicals from lignocelluloses in recent years. Mining new genes from nature, rational engineering of known genes and directed evolution of these genes are required to get tailor-made xylanases for various industrial applications.

摘要

半纤维素的单体糖的酶促解聚需要多种酶的协同作用,其中内切木聚糖酶(EC 3.2.1.8)和β-木糖苷酶(EC 3.2.1.37)(统称木聚糖酶)在木聚糖的解聚中起着至关重要的作用,木聚糖是半纤维素的主要成分。重组蛋白工程的最新进展为在异源和同源宿主中工程化和表达木聚糖酶铺平了道路。内切木聚糖酶在包括细菌、酵母、真菌和植物在内的许多宿主中成功实现了功能表达,酵母是最有前途的表达系统。β-木糖苷酶的功能表达更具挑战性,可能是由于其更复杂的结构。糖苷水解酶家族 10 和 11 的内切木聚糖酶的结构已得到很好的阐明。家族 F/10 内切木聚糖酶由纤维素结合域和催化域组成,通过连接肽连接,具有(β/α)8 折叠 TIM 桶。家族 G/11 内切木聚糖酶具有β-果冻卷结构,由于其较小的分子尺寸,被认为能够穿过半纤维素网络的孔隙。属于糖苷水解酶家族 39 的β-D-木糖苷酶的结构已被阐明为四聚体,每个单体由三个不同的区域组成:具有典型(β/α)8--TIM 桶折叠的催化域、β-夹心结构域和具有酶活性位点的小α-螺旋结构域,该酶活性位点与 D-木寡糖结合位于桶的上侧。糖基化通常被认为是木聚糖酶最重要的翻译后修饰之一,但少数例子表明真核木聚糖酶在细菌中的功能表达。这些协同酶的最佳比例对于提高水解效率和降低酶用量非常重要,但在文献中很少涉及。木聚糖酶在食品、饲料和造纸等传统领域的应用时间较长,但近年来,人们越来越关注利用它们从木质纤维素中生产糖和其他化学品。需要从自然界中挖掘新的基因,对已知基因进行合理的工程改造,并对这些基因进行定向进化,以获得适合各种工业应用的定制木聚糖酶。

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