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嗜纤维梭菌纤维小体的一个恒定组分xynB基因及其产物XynB的分离与表达

Isolation and expression of the xynB gene and its product, XynB, a consistent component of the Clostridium cellulovorans cellulosome.

作者信息

Han Sung Ok, Yukawa Hideaki, Inui Masayuki, Doi Roy H

机构信息

Section of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.

出版信息

J Bacteriol. 2004 Dec;186(24):8347-55. doi: 10.1128/JB.186.24.8347-8355.2004.

Abstract

The nucleotide sequence of the Clostridium cellulovorans xynB gene, which encodes the XynB xylanase, consists of 1,821 bp and encodes a protein of 607 amino acids with a molecular weight of 65,976. XynB contains a typical N-terminal signal peptide of 29 amino acid residues, followed by a 147-amino-acid sequence that is homologous to the family 4-9 (subfamily 9 in family 4) carbohydrate-binding domain. Downstream of this domain is a family 10 catalytic domain of glycosyl hydrolase. The C terminus separated from the catalytic domain by a short linker sequence contains a dockerin domain responsible for cellulosome assembly. The XynB sequence from mass spectrometry and N-terminal amino acid sequence analyses agreed with that deduced from the nucleotide sequence. XynB was highly active toward xylan, but not active toward carboxymethyl cellulose. The enzyme was optimally active at 40 degrees C and pH 5.0. Northern hybridizations revealed that xynB is transcribed as a monocistronic 1.9-kb mRNA. RNA ligase-mediated rapid amplification of 5' cDNA ends by PCR (RLM-5'RACE PCR) analysis of C. cellulovorans RNA identified a single transcriptional start site of xynB located 47 bp upstream from the first nucleotide of the translation initiation codon. Alignment of the xynB promoter region provided evidence for highly conserved sequences that exhibited strong similarity to the sigmaA consensus promoter sequences of gram-positive bacteria. Expression of xynB mRNA increased from early to middle exponential phase and decreased during the early stationary phase when the cells were grown on cellobiose. No alternative promoter was observed by RLM-5'RACE PCR and reverse transcriptase PCR analyses during expression. The analysis of the products from xylan hydrolysis by thin-layer chromatography indicated its endoxylanase activity. The results suggest that XynB is a consistent and major cellulosomal enzyme during growth on cellulose or xylan.

摘要

编码木聚糖酶XynB的嗜纤维梭菌xynB基因的核苷酸序列由1,821个碱基对组成,编码一个607个氨基酸的蛋白质,分子量为65,976。XynB包含一个典型的29个氨基酸残基的N端信号肽,其后是一个与4-9家族(4家族中的9亚家族)碳水化合物结合结构域同源的147个氨基酸序列。该结构域下游是糖基水解酶的10家族催化结构域。通过短连接序列与催化结构域分离的C端包含一个负责纤维小体组装的锚定蛋白结构域。质谱和N端氨基酸序列分析得到的XynB序列与从核苷酸序列推导的序列一致。XynB对木聚糖具有高活性,但对羧甲基纤维素无活性。该酶在40℃和pH 5.0时活性最佳。Northern杂交显示xynB转录为单顺反子1.9 kb mRNA。通过对嗜纤维梭菌RNA进行RNA连接酶介导的5' cDNA末端PCR快速扩增(RLM-5'RACE PCR)分析,确定xynB的单个转录起始位点位于翻译起始密码子第一个核苷酸上游47 bp处。xynB启动子区域的比对为与革兰氏阳性菌的sigmaA共有启动子序列具有高度相似性的高度保守序列提供了证据。当细胞在纤维二糖上生长时,xynB mRNA的表达从指数早期到中期增加,在稳定期早期下降。在表达过程中,RLM-5'RACE PCR和逆转录酶PCR分析未观察到替代启动子。通过薄层色谱对木聚糖水解产物的分析表明其具有内切木聚糖酶活性。结果表明,XynB是在纤维素或木聚糖上生长期间一种稳定且主要的纤维小体酶。

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