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中国明对虾溶菌酶基因克隆、重组表达与性质分析
引用本文:卜兴江,杜欣军,周文杰,赵小凡,王金星. 中国明对虾溶菌酶基因克隆、重组表达与性质分析[J]. 微生物学报, 2008, 24(5): 723-732
作者姓名:卜兴江  杜欣军  周文杰  赵小凡  王金星
作者单位:山东大学生命科学学院, 济南 250100; 安徽师范大学生命科学学院, 芜湖 241000;山东大学生命科学学院, 济南 250100;衡水学院生命科学系, 衡水 053000;山东大学生命科学学院, 济南 250100;山东大学生命科学学院, 济南 250100
基金项目:国家自然科学基金(No. 30770282)和863计划(No. 2007AA09Z425, 2006AA100311)资助。
摘    要:溶菌酶是机体先天免疫系统中一个重要的效应分子, 参与机体多种免疫反应, 在溶菌过程中形成一个水解体系, 破坏和消除侵入体内的病原, 从而实现机体的免疫防御。从中国明对虾中克隆得到了溶菌酶基因(称为FcLyz基因), 该基因全长709 bp, 其完整的阅读框为477 bp, 编码158个氨基酸, 前18个氨基酸(-1~-18)为信号肽, 成熟肽由140个氨基酸组成(1-140aa), 其分子量为16.2 kD。经SMART分析,该基因具有1个溶菌酶1(LYZ1)结构域(19-130aa)。半定量RT-PCR分析结果表明溶菌酶虽在多种组织中有较低水平的组成性表达, 但在细菌诱导的血细胞、心脏、肝胰腺和鳃等多种组织中表达上调。将中国明对虾溶菌酶基因的成熟肽亚克隆进原核表达载体pET-30a (+)中, 转化大肠杆菌BL21(DE3), 再进行诱导表达和亲和纯化, 得到了纯化的重组溶菌酶, 并进行了抑菌活性检测。结果表明, 重组对虾溶菌酶对革兰氏阳性菌的抑菌能力较强, 最小抑菌浓度达到3.43 mmol/L, 但对革兰氏阴性菌抑制作用较小。上述结果表明, 该溶菌酶作为一种重要的免疫效应分子, 参与了对虾的免疫防御反应。

关 键 词:中国明对虾   溶菌酶   先天免疫   重组表达

Molecular Cloning, Recombinant Expression and Characterization of Lysozyme from Chinese Shrimp Fenneropenaeus chinensis
Xingjiang Bu,Xinjun Du,Wenjie Zhou,Xiaofan Zhao and Jinxing Wang. Molecular Cloning, Recombinant Expression and Characterization of Lysozyme from Chinese Shrimp Fenneropenaeus chinensis[J]. Acta microbiologica Sinica, 2008, 24(5): 723-732
Authors:Xingjiang Bu  Xinjun Du  Wenjie Zhou  Xiaofan Zhao  Jinxing Wang
Affiliation:School of Life Sciences, Shandong University, Jinan 250100, China; School of Life Sciences, Anhui Normal University, Wuhu 241000, China;School of Life Sciences, Shandong University, Jinan 250100, China;Department of Life Scences, Hengshui College, Hengshui 053000, China;School of Life Sciences, Shandong University, Jinan 250100, China;School of Life Sciences, Shandong University, Jinan 250100, China
Abstract:Lysozyme hydrolyses bacterial cell walls and acts as a nonspecific innate immunity molecule against the invasion of bacterial pathogens. We cloned the cDNA of lysozyme from Fenneropenaeus chinensis and named Fc-lysozyme (FcLyz in short). The full length of the gene was of 709 bp, and the open reading frame (477 bp) encoded 158 amino acids. The predicted protein had a signal peptide (-1~ -18 residue) and molecular weight of the mature protein (residue 1~140) was of 16.2 kD. A Lyz 1 domain (residue 1~130) in the lysozyme was found by SMART analysis. The results of semiquantity RT-PCR showed that FcLyz was constitutively expressed in tested tissues in a low level in normal shrimp, and up-regulated in hemocytes, heart, hepatopancreas and gill of bacterial challenged shrimp. The DNA fragment of mature Fc-Lys was subcloned to pET-30a (+) expression vector, the recombinant plasmid was transformed into Escherichia coli BL21 (DE3) and then induced by isopropylthio-b-D-galactoside (IPTG). The antibacterial activity of the purified recombinant FcLys was analyzed and minimal inhibitory concentration (MIC) was assayed. The recombinant protein showed high antibacterial activity against some Gram-positive bacteria, and MIC reached 3.43 mmol/L, and relatively low activity against Gram-negative bacteria. All together, the Fc-Lys was regulated by pathogen infection and had anti- bacterial activity. This suggested that the FcLyz may be one of the important molecules against pathogens in innate immunity of the shrimp.
Keywords:Chinese shrimp (Fenneropenaeus chinensis)   lysozyme   innate immunity   recombinant expression
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