A bifunctional invertebrate-type lysozyme from the disk abalone, Haliotis discus discus: Genome organization, transcriptional profiling and biological activities of recombinant protein

被引:36
作者
Bathige, S. D. N. K. [1 ]
Umasuthan, Navaneethaiyer [1 ]
Kasthuri, Saranya Revathy [1 ]
Whang, Ilson [1 ]
Lim, Bong-Soo [2 ]
Nam, Bo-Hye [3 ]
Lee, Jehee [1 ,2 ]
机构
[1] Jeju Natl Univ, Sch Marine Biomed Sci, Dept Marine Life Sci, Cheju 690756, Jeju Self Gover, South Korea
[2] Jeju Natl Univ, Marine & Environm Inst, Cheju 690814, Jeju Self Gover, South Korea
[3] Natl Fisheries Res & Dev Inst, Biotechnol Res Div, Pusan 619705, South Korea
关键词
Invertebrate-type lysozyme; Haliotis discus discus; Genomic structure; Lytic activity; Isopeptidase activity; Immune response; GOOSE-TYPE LYSOZYME; C-TYPE; MOLECULAR CHARACTERIZATION; DIVERSICOLOR-SUPERTEXTA; EXPRESSION ANALYSIS; VIRUS-INFECTION; GENE; CLONING; OYSTER; IDENTIFICATION;
D O I
10.1016/j.dci.2013.06.009
中图分类号
S9 [水产、渔业];
学科分类号
090805 [渔业资源学];
摘要
Lysozyme is an important enzyme in the innate immune system that plays a vital role in fighting microbial infections. In the current study, we identified, cloned, and characterized a gene that encodes an invertebrate-type lysozyme from the disk abalone, Haliotis discus discus (abLysI). The full-length cDNA of abLysl consisted of 545 bp with an open reading frame of 393 bp that encodes 131 amino acids. The theoretical molecular mass of mature abLysI was 12.3 kDa with an isoelectric point of 8.03. Conserved features in other homologs, such as catalytic sites for lytic activity (Glu(30) and Asp(41)), isopeptidase activity (His(107)), and ten cysteine residues were identified in abLysl. Genomic sequence analysis with respect to its cDNA showed that abLysl was organized into four exons interrupted by three introns. Several immune-related transcription factor binding sites were discovered in the putative promoter region. Homology and phylogeny analysis of abLysl depicted high identity and closer proximity, respectively, with an annelid i-type lysozyme from Hirudo medicinalis, and indicated that abLysI is a novel molluscan i-type lysozyme. Tissue-specific expressional studies revealed that abLysl is mainly transcribed in hepatopancreas followed by mantle. In addition, abLysl mRNA expression was induced following bacterial (Vibrio parahaemolyticus and Listeria monocytogenes) and viral (viral hemorrhagic septicemia virus) challenges. Recombinantly expressed abLysI [(r)abLysI] demonstrated strong lytic activity against Micro coccus lysodeikticus, isopeptidase activity, and antibacterial activity against several Gram-positive and Gram-negative bacteria. Moreover, (r)abLysI showed optimum lytic activity at pH 4.0 and 60 degrees C, while exhibiting optimum isopeptidase activity at pH 7.0. Taken together, these results indicate that abLysI is potentially involved in immune responses of the disk abalone to protect it from invaders. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:282 / 294
页数:13
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