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牙龈卟啉菌牙龈蛋白酶K的基因克隆和序列分析
引用本文:张凤秋, 杨连甲, 吴织芬, 杨聚才,. 牙龈卟啉菌牙龈蛋白酶K的基因克隆和序列分析[J]. 微生物学通报, 2004, 31(1): 79-81
作者姓名:张凤秋   杨连甲   吴织芬   杨聚才  
作者单位:第四军医大学口腔医学院,西安,710032
摘    要:利用PCR方法 ,分别扩增牙龈卟啉菌牙龈蛋白酶K (KGP)的催化结构域 (KGPcd)和凝集素结构域 (KGP-hag)的基因片段 ,将基因片段插入pGEM-T easyVector,通过限制性酶切和核苷酸序列分析鉴定, KGPcdKGP hag的序列与国外文献报道一致。克隆到牙龈卟啉菌KGPKGPcdKGP hag基因 ,为体外表达其活性蛋白奠定了基础。

关 键 词:牙龈卟啉菌   牙龈蛋白酶K   序列测定和分析  
文章编号:0253-2654(2004)01-0079-03
修稿时间:2002-11-11

CLONING AND SEQUENCING ANALYSIS OF GINGIPAIN K OF PORPHYROMONAS GINGIVALIS
ZHANG Feng-Qiu YANG Lian-Jia WU Zhi-Fen YANG Ju-Cai. CLONING AND SEQUENCING ANALYSIS OF GINGIPAIN K OF PORPHYROMONAS GINGIVALIS[J]. Microbiology China, 2004, 31(1): 79-81
Authors:ZHANG Feng-Qiu YANG Lian-Jia WU Zhi-Fen YANG Ju-Cai
Abstract:The desired DNA product of KGPcd and KGP-hag was obtained from the total DNA of Porphyromonas gingivalis by PCR with two pairs of gene specific primers. The segment of KGPcd and KGP-hag (about 1.5kb and 1.6kb) was inserted into pGEM-T easy Vector. The double-stranded DNA of the postitive clone was analyzed by restriction endonuclease mapping and DNA sequenceing. The sequences of KGPcd and KGP-hag were consistent with those of the references appeared. The proteins of KGPcd and KGP-hag will be obtained for further study.
Keywords:Porphyromonas gingivalis  Gingipain K  Sequencing and Characterization  
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