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Isolation and Expression of the xynB Gene and Its Product XynB a Consistent Component of the Clostridium cellulovorans Cellulosome

机译:xynB基因及其产物XynB的分离和表达Cyntricell Cellulovorans Cellulosome的一致组成部分

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摘要

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°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 σA 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.
机译:纤维梭菌xynB基因的核苷酸序列,编码XynB木聚糖酶,由1,821 bp组成,编码607个氨基酸的蛋白质,分子量为65,976。 XynB包含一个典型的N端信号肽,含29个氨基酸残基,后跟一个与4-9族(4族中的9族)碳水化合物结合域同源的147个氨基酸序列。该结构域的下游是糖基水解酶的10族催化结构域。通过短连接子序列与催化结构域隔开的C末端包含负责纤维素小体组装的dockerin结构域。质谱和N末端氨基酸序列分析得出的XynB序列与核苷酸序列推导的序列一致。 XynB对木聚糖具有高活性,但对羧甲基纤维素则无活性。该酶在40°C和pH 5.0时具有最佳活性。 Northern杂交揭示xynB被转录为单顺反子1.9-kb mRNA。 RNA连接酶介导的5'cDNA末端的快速扩增通过PCR(RLM-5'RACE PCR)对C.纤维素核糖核酸的分析确定了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。 xynB启动子区域的比对为高度保守的序列提供了证据,该序列与革兰氏阳性细菌的σ A 共有启动子序列具有很强的相似性。当细胞在纤维二糖上生长时,xynB mRNA的表达从早期到中期指数期增加,而在早期静止期减少。在表达过程中,通过RLM-5'RACE PCR和逆转录酶PCR分析未观察到其他启动子。通过薄层色谱法对木聚糖水解产物的分析表明其内切木聚糖酶活性。结果表明,XynB是在纤维素或木聚糖上生长期间一致且主要的纤维素酶。

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