Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13880
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dc.contributor.authorDonpudsa S.
dc.contributor.authorVisetnan S.
dc.contributor.authorSupungul P.
dc.contributor.authorTang S.
dc.contributor.authorTassanakajon A.
dc.contributor.authorRimphanitchayakit V.
dc.date.accessioned2021-04-05T03:32:34Z-
dc.date.available2021-04-05T03:32:34Z-
dc.date.issued2014
dc.identifier.issn0145305X
dc.identifier.other2-s2.0-84904880634
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/13880-
dc.identifier.urihttps://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.abstractAn 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.subjecthumoral antibody
dc.subjectkanamycin
dc.subjectrecombinant crustinPm4 1 protein
dc.subjectrecombinant protein
dc.subjectthioredoxin
dc.subjecttype 1 crustin
dc.subjecttype 2 crustin
dc.subjectunclassified drug
dc.subjectantimicrobial cationic peptide
dc.subjectarthropod protein
dc.subjectamino terminal sequence
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectantimicrobial activity
dc.subjectantiviral activity
dc.subjectarticle
dc.subjectBacillus megaterium
dc.subjectBacillus subtilis
dc.subjectbacterial growth
dc.subjectblood cell
dc.subjectcontrolled study
dc.subjectDNA virus infection
dc.subjectdrug effect
dc.subjectEscherichia coli
dc.subjectgene expression regulation
dc.subjectgenetic variability
dc.subjectgrowth inhibition
dc.subjectLD 50
dc.subjectMicrococcus luteus
dc.subjectnonhuman
dc.subjectnucleotide sequence
dc.subjectPenaeus monodon
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectsequence analysis
dc.subjectStaphylococcus aureus
dc.subjectupregulation
dc.subjectVibrio harveyi
dc.subjectWhite spot syndrome virus
dc.subjectamino acid sequence
dc.subjectanimal
dc.subjectcell culture
dc.subjectchemistry
dc.subjectgenetic variability
dc.subjectgenetics
dc.subjectimmunology
dc.subjectmicrobiology
dc.subjectmolecular genetics
dc.subjectPenaeidae
dc.subjectsequence alignment
dc.subjectvirology
dc.subjectAmino Acid Sequence
dc.subjectAnimals
dc.subjectAntimicrobial Cationic Peptides
dc.subjectArthropod Proteins
dc.subjectCells, Cultured
dc.subjectGenetic Variation
dc.subjectHemocytes
dc.subjectMolecular Sequence Data
dc.subjectPenaeidae
dc.subjectSequence Alignment
dc.titleType I and type II crustins from Penaeus monodon, genetic variation and antimicrobial activity of the most abundant crustinPm4
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationDevelopmental and Comparative Immunology. Vol 47, No.1 (2014), p.95-103
dc.identifier.doi10.1016/j.dci.2014.06.015
Appears in Collections:Scopus 1983-2021

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