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

Author:
Bathige, S.D.N.K., Umasuthan, Navaneethaiyer, Kasthuri, Saranya Revathy, Whang, Ilson, Lim, Bong-Soo, Nam, Bo-Hye, Lee, Jehee
Source:
Developmental and comparative immunology 2013 v.41 no.2 pp. 282-294
ISSN:
0145-305X
Subject:
Gram-negative bacteria, Haliotis discus, Hirudo medicinalis, Listeria monocytogenes, Micrococcus luteus, Vibrio parahaemolyticus, Viral hemorrhagic septicemia virus, abalone, active sites, antibacterial properties, binding sites, complementary DNA, cysteine, exons, gene expression, genes, hepatopancreas, immune response, innate immunity, introns, isoelectric point, lysozyme, messenger RNA, molecular weight, open reading frames, pH, phylogeny, promoter regions, recombinant proteins, sequence analysis, transcription (genetics), transcription factors
Abstract:
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 545bp with an open reading frame of 393bp that encodes 131 amino acids. The theoretical molecular mass of mature abLysI was 12.3kDa with an isoelectric point of 8.03. Conserved features in other homologs, such as catalytic sites for lytic activity (Glu30 and Asp41), isopeptidase activity (His107), 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.
Agid:
947292