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DC Field | Value | Language |
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dc.contributor.author | Donpudsa S. | |
dc.contributor.author | Visetnan S. | |
dc.contributor.author | Supungul P. | |
dc.contributor.author | Tang S. | |
dc.contributor.author | Tassanakajon A. | |
dc.contributor.author | Rimphanitchayakit V. | |
dc.date.accessioned | 2021-04-05T03:32:34Z | - |
dc.date.available | 2021-04-05T03:32:34Z | - |
dc.date.issued | 2014 | |
dc.identifier.issn | 0145305X | |
dc.identifier.other | 2-s2.0-84904880634 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13880 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904880634&doi=10.1016%2fj.dci.2014.06.015&partnerID=40&md5=c7058ef3605abcd19f09aefb0032cf6d | |
dc.description.abstract | An antimicrobial protein, crustin, is involved in the innate immunity of crustacean by defending the host directly against the microbial pathogens. By data mining the Penaeus monodon EST database, two type I crustins, carcinin. Pm1 and 2, and ten type II crustins, crustin. Pm1-10, were identified. The abundant crustins were crustin. Pm1, 4 and 7, each with variation in the length of Gly-rich repeat among its members. A few crustin. Pm1, 4 and 7 with deletion in the Cys-rich region were also observed. Furthermore, the crustin. Pm4 with the longest N-terminal Gly-rich region was characterized. The crustinPm4 allelic genes were expressed mainly from the hemocytes. Its expression was up-regulated readily by WSSV infection and gradually decreased to normal level afterwards. The recombinant crustin. Pm4-1 (rcrustin. Pm4-1) isoform was produced using the Escherichia coli expression system and tested for its antimicrobial activity. The rcrustin. Pm4-1 was able to inhibit the growth of a Gram-positive bacterium, Bacillus megaterium but not Bacillus subtilis, Micrococcus luteus and Staphylococcus aureus. It also inhibited the growth of two Gram-negative bacteria, E. coli 363 and Vibrio harveyi 639 at lower potency. The rcrustin. Pm4-1 affected the WSSV infection because the expression of an intermediate early gene ie1 in WSSV-infected hemocyte cell culture was reduced. It was shown further that the rcrustin. Pm4-1 could delay by about one and a half days the manifestation of disease by WSSV. © 2014 Elsevier Ltd. | |
dc.subject | humoral antibody | |
dc.subject | kanamycin | |
dc.subject | recombinant crustinPm4 1 protein | |
dc.subject | recombinant protein | |
dc.subject | thioredoxin | |
dc.subject | type 1 crustin | |
dc.subject | type 2 crustin | |
dc.subject | unclassified drug | |
dc.subject | antimicrobial cationic peptide | |
dc.subject | arthropod protein | |
dc.subject | amino terminal sequence | |
dc.subject | animal cell | |
dc.subject | animal experiment | |
dc.subject | animal tissue | |
dc.subject | antimicrobial activity | |
dc.subject | antiviral activity | |
dc.subject | article | |
dc.subject | Bacillus megaterium | |
dc.subject | Bacillus subtilis | |
dc.subject | bacterial growth | |
dc.subject | blood cell | |
dc.subject | controlled study | |
dc.subject | DNA virus infection | |
dc.subject | drug effect | |
dc.subject | Escherichia coli | |
dc.subject | gene expression regulation | |
dc.subject | genetic variability | |
dc.subject | growth inhibition | |
dc.subject | LD 50 | |
dc.subject | Micrococcus luteus | |
dc.subject | nonhuman | |
dc.subject | nucleotide sequence | |
dc.subject | Penaeus monodon | |
dc.subject | priority journal | |
dc.subject | protein expression | |
dc.subject | sequence analysis | |
dc.subject | Staphylococcus aureus | |
dc.subject | upregulation | |
dc.subject | Vibrio harveyi | |
dc.subject | White spot syndrome virus | |
dc.subject | amino acid sequence | |
dc.subject | animal | |
dc.subject | cell culture | |
dc.subject | chemistry | |
dc.subject | genetic variability | |
dc.subject | genetics | |
dc.subject | immunology | |
dc.subject | microbiology | |
dc.subject | molecular genetics | |
dc.subject | Penaeidae | |
dc.subject | sequence alignment | |
dc.subject | virology | |
dc.subject | Amino Acid Sequence | |
dc.subject | Animals | |
dc.subject | Antimicrobial Cationic Peptides | |
dc.subject | Arthropod Proteins | |
dc.subject | Cells, Cultured | |
dc.subject | Genetic Variation | |
dc.subject | Hemocytes | |
dc.subject | Molecular Sequence Data | |
dc.subject | Penaeidae | |
dc.subject | Sequence Alignment | |
dc.title | Type I and type II crustins from Penaeus monodon, genetic variation and antimicrobial activity of the most abundant crustinPm4 | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Developmental and Comparative Immunology. Vol 47, No.1 (2014), p.95-103 | |
dc.identifier.doi | 10.1016/j.dci.2014.06.015 | |
Appears in Collections: | Scopus 1983-2021 |
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