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芽孢杆菌属JDR-2菌株木聚糖利用系统的转录组分析

Transcriptomic analysis of xylan utilization systems in Paenibacillus sp. strain JDR-2.

作者信息

Sawhney Neha, Crooks Casey, St John Franz, Preston James F

出版信息

Appl Environ Microbiol. 2015 Feb;81(4):1490-501. doi: 10.1128/AEM.03523-14.

Abstract

Xylans, including methylglucuronoxylans (MeGX(n)) and methylglucuronoarabinoxylans (MeGAXn), are the predominant polysaccharidesin hemicellulose fractions of dicots and monocots available for conversion to biofuels and chemicals. Paenibacillus sp. strain JDR-2 (Pjdr2) efficiently depolymerizes MeGX(n) and MeGAX(n) and assimilates the generated oligosaccharides, resulting in efficient saccharification and subsequent metabolism of these polysaccharides. A xylan utilization regulon encoding a cellassociated GH10 (glycoside hydrolase family 10) endoxylanase, transcriptional regulators, ABC (ATP binding cassette) transporters, an intracellular GH67 -glucuronidase, and other glycoside hydrolases contributes to complete metabolism. This GH10/GH67 system has been proposed to account for preferential utilization of xylans compared to free oligo- and monosaccharides. To identify additional genes contributing to MeGX(n) and MeGAXn utilization, the transcriptome of Pjdr2 has been sequenced following growth on each of these substrates as well as xylose and arabinose. Increased expression of genes with different substrates identified pathways common or unique to the utilization of MeGX(n) or MeGAX(n). Coordinate upregulation of genes comprising the GH10/GH67 xylan utilization regulon is accompanied with upregulation of genes encoding a GH11 endoxylanase and a GH115 -glucuronidase, providing evidence for a novel complementary pathway for processing xylans. Elevated expression of genes encoding a GH43 arabinoxylan arabinofuranohydrolase and an arabinose ABC transporter on MeGAX(n) but not on MeGX(n) supports a process in which arabinose may be removed extracellularly followed by its rapid assimilation.Further development of Pjdr2 for direct conversion of xylans to targeted products or introduction of these systems into fermentative strains of related bacteria may lead to biocatalysts for consolidated bioprocessing of hemicelluloses released from lignocellulose.

摘要

木聚糖,包括甲基葡萄糖醛酸木聚糖(MeGX(n))和甲基葡萄糖醛酸阿拉伯木聚糖(MeGAXn),是双子叶植物和单子叶植物半纤维素组分中的主要多糖,可用于转化为生物燃料和化学品。芽孢杆菌属菌株JDR-2(Pjdr2)能有效地使MeGX(n)和MeGAX(n)解聚,并同化产生的寡糖,从而实现这些多糖的高效糖化及后续代谢。一个编码细胞相关的GH10(糖苷水解酶家族10)内切木聚糖酶、转录调节因子、ABC(ATP结合盒)转运蛋白、一种细胞内GH67 -葡萄糖醛酸酶及其他糖苷水解酶的木聚糖利用操纵子有助于实现完全代谢。有人提出,与游离寡糖和单糖相比,这种GH10/GH67系统可解释木聚糖的优先利用。为了鉴定有助于利用MeGX(n)和MeGAXn的其他基因,已对Pjdr2在这些底物以及木糖和阿拉伯糖上生长后的转录组进行了测序。不同底物条件下基因表达的增加确定了MeGX(n)或MeGAX(n)利用过程中的共同或独特途径。构成GH10/GH67木聚糖利用操纵子的基因协同上调,同时编码GH11内切木聚糖酶和GH115 -葡萄糖醛酸酶的基因也上调,这为处理木聚糖的新互补途径提供了证据。编码GH43阿拉伯木聚糖阿拉伯呋喃水解酶和阿拉伯糖ABC转运蛋白的基因在MeGAX(n)上表达升高,但在MeGX(n)上不升高,这支持了一种过程,即阿拉伯糖可能在细胞外被去除,随后迅速被同化。进一步开发Pjdr2以将木聚糖直接转化为目标产物,或将这些系统引入相关细菌的发酵菌株中,可能会产生用于木质纤维素释放的半纤维素联合生物加工的生物催化剂。

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