Department of Marine Life Sciences, School of Marine Biomedical Sciences, Jeju National University, Jeju Self-Governing Province 690-756, Republic of Korea.
Dev Comp Immunol. 2013 Oct;41(2):282-94. doi: 10.1016/j.dci.2013.06.009. Epub 2013 Jun 22.
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 abLysI 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 abLysI. Genomic sequence analysis with respect to its cDNA showed that abLysI 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 abLysI 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 abLysI is mainly transcribed in hepatopancreas followed by mantle. In addition, abLysI 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 Micrococcus 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 °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.
溶菌酶是先天免疫系统中的一种重要酶,在抵抗微生物感染方面发挥着至关重要的作用。在本研究中,我们从盘鲍(Haliotis discus discus)中鉴定、克隆并表征了一种编码无脊椎动物溶菌酶的基因(abLysI)。abLysI 的全长 cDNA 由 545bp 组成,开放阅读框为 393bp,编码 131 个氨基酸。成熟 abLysI 的理论分子质量为 12.3 kDa,等电点为 8.03。abLysI 中鉴定到其他同源物的保守特征,如溶菌活性的催化位点(Glu(30)和 Asp(41))、肽酶活性(His(107))和 10 个半胱氨酸残基。其 cDNA 的基因组序列分析表明,abLysI 由四个外显子组成,被三个内含子打断。在假定的启动子区域发现了几个免疫相关转录因子结合位点。abLysI 的同源性和系统发育分析分别显示与医用水蛭的 annelid i 型溶菌酶具有高度的同一性和更接近的亲缘关系,表明 abLysI 是一种新型的软体动物 i 型溶菌酶。组织特异性表达研究表明,abLysI 主要在肝胰腺中转录,其次是套膜。此外,abLysI mRNA 的表达在受到细菌(副溶血弧菌和单核细胞增生李斯特菌)和病毒(病毒性出血性败血症病毒)挑战后被诱导。重组表达的 abLysI[(r)abLysI]对微球菌溶菌酶表现出强烈的溶菌活性、肽酶活性和对几种革兰氏阳性和革兰氏阴性菌的抗菌活性。此外,(r)abLysI 在 pH4.0 和 60°C 时表现出最佳的溶菌活性,而在 pH7.0 时表现出最佳的肽酶活性。总之,这些结果表明 abLysI 可能参与了盘鲍的免疫反应,以保护其免受入侵者的侵害。