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作 者:Yingzhu WEI Zhiqing WEI Xuelian LIN Huanying PANG Na WANG
机构地区:[1]Fisheries College,Guangdong Ocean University,Zhanjiang 524025,China [2]Guangdong Provincial Key Laboratory of Aquatic Animal Disease Control and Healthy Culture&Key Laboratory of Control for Diseases of Aquatic Economic Animals of Guangdong Higher Education Institutes,Zhanjiang 524025,China [3]Chinese Academy of Inspection and Quarantine,Beijing 100176,China
出 处:《Asian Agricultural Research》2024年第8期32-37,共6页亚洲农业研究(英文)
基 金:Supported by National Natural Science Foundation of China(32073015);Graduate Education Innovation Program of Guangdong Province(YJYH[2022]1);Undergraduate Innovation and Entrepreneurship Training Program of Guangdong Ocean University(CXXL2024007);Undergraduate Innovation Team of Guangdong Ocean University(CCTD201802).
摘 要:[Objectives]To clone the sucC gene of Vibrio alginolyticus strain HY9901 and conduct the bioinformatics analysis.[Methods]Based on the sucC gene of V.alginolyticus strain HY9901,specific primers were designed to amplify the full length sequence by PCR and make further analysis.[Results]The theoretical molecular weight of SucC protein was about 41528.45 Da,and the full length was 1167 bp,encoding 388 amino acids.It has no signal peptide and transmembrane region,and has a variety of functional sites.It is predicted that it is mainly located in the cytoplasm,and the ubiquitin and lactate modification sites overlap,and it has high gene homology with Vibrio parahaemolyticus.Theα-helix,random coil and extended strand are the main secondary structures.The similarity between the constructed three-level structure model and the template is high.[Conclusions]This study reveals the structural characteristics and functional potential of SucC protein,and provides a theoretical basis for the study of drug resistance mechanism and prevention strategies.
关 键 词:VIBRIO ALGINOLYTICUS GENE amplification sucC GENE Succinyl-Coa SYNTHETASE Protein POST-TRANSLATIONAL modification Bioinformatics analysis
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