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中国对虾几丁质酶(Fcchi-3)的分子特征和表达分析。

Molecular characterization and expression analysis of chitinase (Fcchi-3) from Chinese shrimp, Fenneropenaeus chinensis.

机构信息

Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, People's Republic of China.

出版信息

Mol Biol Rep. 2010 Apr;37(4):1913-21. doi: 10.1007/s11033-009-9633-0. Epub 2009 Jul 30.

Abstract

Complementary DNA (cDNA) and genomic DNA, including flanking regions of the chitinase gene (Fcchi-3) of Fenneropenaeus chinensis, were cloned and sequenced. Fcchi-3 was found to have 92.0 and 91.4% identity at the cDNA level to that of Litopenaeus vannamei and Marsupenaeus japonicus, respectively. The predicted amino acid sequence had an overall similarity with a comparable region of L. vannamei (96.8%) and M. japonicus (93.4%). Based on the cDNA sequence, the genomic structure of the gene was characterized. Sequence analysis revealed that the Fcchi-3 gene was composed of seven exons with 411, 252, 186, 132, 171, 117 and 135 bp and six introns with 232, 196, 121, 90, 159 and 157 bp. Analysis by RT-PCR revealed that Fcchi-3 was a hepatopancreas specific gene. Semi-quantitative RT-PCR analysis revealed that Fcchi-3 transcript was down-regulated significantly in response to the challenge of WSSV at 5 h post-injection and then came back to normal level at 37 h. A fusion protein containing Fcchi-3 was produced and the purified recombinant protein exhibited similar biological function. The result of identification through LC-ESI-MS showed that three peptide fragments (-MAADPVLR-, -ATIDPAYNVPELSK- and -AILAVGGWNEGSPK-) of the recombinant protein were identical to the corresponding sequence of L. vannamei chitinase-3. The recombinant Fcchi-3 could degrade the colloid chitin confirming that the recombinant protein is actually the chitinase.

摘要

对中国对虾几丁质酶基因(Fcchi-3)的 cDNA 和基因组 DNA,包括侧翼序列进行了克隆和测序。Fcchi-3 在 cDNA 水平上与凡纳滨对虾和日本囊对虾的同源性分别为 92.0%和 91.4%。预测的氨基酸序列与凡纳滨对虾(96.8%)和日本囊对虾(93.4%)的可比区域具有总体相似性。基于 cDNA 序列,对基因的基因组结构进行了表征。序列分析表明,Fcchi-3 基因由七个外显子组成,其长度分别为 411、252、186、132、171、117 和 135bp,六个内含子分别为 232、196、121、90、159 和 157bp。RT-PCR 分析显示,Fcchi-3 是一种肝胰腺特异性基因。半定量 RT-PCR 分析显示,Fcchi-3 转录物在 WSSV 攻击后 5 小时显著下调,然后在 37 小时恢复正常水平。表达并纯化了含有 Fcchi-3 的融合蛋白,该重组蛋白表现出相似的生物学功能。LC-ESI-MS 的鉴定结果表明,重组蛋白的三个肽段(-MAADPVLR-、-ATIDPAYNVPELSK-和-AILAVGGWNEGSPK-)与凡纳滨对虾几丁质酶-3 的相应序列相同。重组 Fcchi-3 可以降解胶体几丁质,证实该重组蛋白实际上是几丁质酶。

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