Han Ji Hee, Lee Kwang Sik, Li Jianhong, Kim Iksoo, Je Yeon Ho, Kim Doh Hoon, Sohn Hung Dae, Jin Byung Rae
College of Natural Resources and Life Science, Dong-A University, Busan 604-714, Korea.
Comp Biochem Physiol B Biochem Mol Biol. 2005 Mar;140(3):427-35. doi: 10.1016/j.cbpc.2004.11.009.
A fat body-specific chitinase cDNA was cloned from the spider, Araneus ventricosus. The cDNA encoding A. ventricosus chitinase (AvChit1) is 1515 bp long with an open reading frame (ORF) of 431 amino acid residues. AvChit1 possesses the chitinase family 18 active site signature and one N-glycosylation site. The deduced amino acid sequence of AvChit1 cDNA showed 43% identity to both Glossina morsitans morsitans chitinase and a human chitotriosidase, and 30-40% to some insect chitinases which lack both the serine/threonine and chitin binding domains. Southern blot analysis of genomic DNA suggested the presence of AvChit1 gene as a single copy. Northern and Western blot analysis and enzyme activity assay showed the tissue-specific expression of AvChit1 in the A. ventricosus fat body. The AvChit1 cDNA was expressed as a 61 kDa polypeptide in baculovirus-infected insect Sf9 cells and the recombinant AvChit1 showed activity in the chitinase enzyme assay using 0.1% glycol chitin as a substrate. Treatment of recombinant virus-infected Sf9 cells with tunicamycin, a specific inhibitor of N-glycosylation, revealed that AvChit1 is N-glycosylated, but the carbohydrate moieties are not essential for chitinolytic activity.
从蜘蛛大腹园蛛中克隆出一个脂肪体特异性几丁质酶cDNA。编码大腹园蛛几丁质酶(AvChit1)的cDNA长1515 bp,具有一个431个氨基酸残基的开放阅读框(ORF)。AvChit1具有18家族几丁质酶活性位点特征和一个N - 糖基化位点。AvChit1 cDNA推导的氨基酸序列与采采蝇几丁质酶和人几丁质三糖苷酶的序列一致性均为43%,与一些缺乏丝氨酸/苏氨酸和几丁质结合结构域的昆虫几丁质酶的序列一致性为30 - 40%。基因组DNA的Southern印迹分析表明AvChit1基因以单拷贝形式存在。Northern和Western印迹分析以及酶活性测定显示AvChit1在大腹园蛛脂肪体中存在组织特异性表达。AvChit1 cDNA在杆状病毒感染的昆虫Sf9细胞中表达为一个61 kDa的多肽,重组AvChit1在以0.1%乙二醇几丁质为底物的几丁质酶活性测定中显示出活性。用N - 糖基化特异性抑制剂衣霉素处理重组病毒感染的Sf9细胞,结果表明AvChit1是N - 糖基化的,但碳水化合物部分对几丁质分解活性并非必需。