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Characterization of a c-type lysozyme of Scophthalmus maximus: Expression, activity, and antibacterial effect
Yu, Lan-ping1,2; Sun, Bo-guang1; Li, Jun1,3; Sun, Li1; Sun, L
2013
发表期刊FISH & SHELLFISH IMMUNOLOGY
ISSN1050-4648
卷号34期号:1页码:46-54
文章类型Article
摘要Lysozyme is a key component of the innate immune system and plays an important role in antibacterial infection. In this study, we analyzed the expression and activity of a chicken-type (c-type) lysozyme (named SmLysC) from turbot (Scophthalmus maximus). SmLysC is composed of 143 residues and shares 67-90% overall sequence identities with the c-type lysozymes of a number of teleost fish. SmLysC possesses a typical c-type lysozyme domain, which contains the conserved residues E50 and D67 that form the putative catalytic site. SmLysC expression was detected, in increasing order, in head kidney, gill, heart, muscle, brain, spleen, blood, and liver. Bacterial infection caused significant inductions of SmLysC expression in head kidney, spleen, and liver in a time-dependent manner. Immunoblot analysis indicated that SmLysC has a subcellular localization in the extracellular milieu. Recombinant SmLysC (rSmLysC) was able to bind to bacterial cells and inhibit bacterial growth. Enzyme assay showed that the optimal temperature and pH of rSmLysC were 37 degrees C and pH 6.0 respectively. In contrast to rSmLysC, the mutant protein rSmLysCM1, which bears alanine substitutions at E50 and D67, displayed drastically reduced bacteriolytic activity. rSmLysC was able to inhibit the growth of several fish bacterial pathogens in a manner that depended on the dose of the protein; however, Gram-positive bacteria were in general more sensitive to rSmLysC than Gram-negative bacteria. Together these results indicate that SmLysC is a functional lysozyme that is likely to participate in innate immune defense against extracellular bacterial pathogens, in particular those of Gram-positive nature. (c) 2012 Elsevier Ltd. All rights reserved.; Lysozyme is a key component of the innate immune system and plays an important role in antibacterial infection. In this study, we analyzed the expression and activity of a chicken-type (c-type) lysozyme (named SmLysC) from turbot (Scophthalmus maximus). SmLysC is composed of 143 residues and shares 67-90% overall sequence identities with the c-type lysozymes of a number of teleost fish. SmLysC possesses a typical c-type lysozyme domain, which contains the conserved residues E50 and D67 that form the putative catalytic site. SmLysC expression was detected, in increasing order, in head kidney, gill, heart, muscle, brain, spleen, blood, and liver. Bacterial infection caused significant inductions of SmLysC expression in head kidney, spleen, and liver in a time-dependent manner. Immunoblot analysis indicated that SmLysC has a subcellular localization in the extracellular milieu. Recombinant SmLysC (rSmLysC) was able to bind to bacterial cells and inhibit bacterial growth. Enzyme assay showed that the optimal temperature and pH of rSmLysC were 37 degrees C and pH 6.0 respectively. In contrast to rSmLysC, the mutant protein rSmLysCM1, which bears alanine substitutions at E50 and D67, displayed drastically reduced bacteriolytic activity. rSmLysC was able to inhibit the growth of several fish bacterial pathogens in a manner that depended on the dose of the protein; however, Gram-positive bacteria were in general more sensitive to rSmLysC than Gram-negative bacteria. Together these results indicate that SmLysC is a functional lysozyme that is likely to participate in innate immune defense against extracellular bacterial pathogens, in particular those of Gram-positive nature. (c) 2012 Elsevier Ltd. All rights reserved.
关键词C-type Lysozyme Scophthalmus Maximus Bacteriolytic Catalytic Site
学科领域Fisheries ; Immunology ; Marine & Freshwater Biology ; Veterinary Sciences
DOI10.1016/j.fsi.2012.10.007
URL查看原文
收录类别SCI
语种英语
WOS研究方向Fisheries ; Immunology ; Marine & Freshwater Biology ; Veterinary Sciences
WOS类目Fisheries ; Immunology ; Marine & Freshwater Biology ; Veterinary Sciences
WOS记录号WOS:000314743600006
WOS关键词GOOSE-TYPE LYSOZYME ; MOLECULAR CHARACTERIZATION ; IMMUNOPROTECTIVE ANALYSIS ; VACCINE CANDIDATE ; CDNA ; IDENTIFICATION ; PHYLOGENY ; INFECTION ; PATTERN ; ANTIGEN
WOS标题词Science & Technology ; Life Sciences & Biomedicine
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被引频次:49[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/16538
专题实验海洋生物学重点实验室
通讯作者Sun, L
作者单位1.Chinese Acad Sci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
2.Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
3.Lake Super State Univ, Sch Biol Sci, Sault Ste Marie, MI USA
第一作者单位实验海洋生物学重点实验室
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Yu, Lan-ping,Sun, Bo-guang,Li, Jun,et al. Characterization of a c-type lysozyme of Scophthalmus maximus: Expression, activity, and antibacterial effect[J]. FISH & SHELLFISH IMMUNOLOGY,2013,34(1):46-54.
APA Yu, Lan-ping,Sun, Bo-guang,Li, Jun,Sun, Li,&Sun, L.(2013).Characterization of a c-type lysozyme of Scophthalmus maximus: Expression, activity, and antibacterial effect.FISH & SHELLFISH IMMUNOLOGY,34(1),46-54.
MLA Yu, Lan-ping,et al."Characterization of a c-type lysozyme of Scophthalmus maximus: Expression, activity, and antibacterial effect".FISH & SHELLFISH IMMUNOLOGY 34.1(2013):46-54.
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