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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2005-5-23
pubmed:databankReference
pubmed:abstractText
A full-length zebrafish (Danio rerio) cytochrome P450 (CYP) 2K6 cDNA, was obtained (GenBank accession No. AF283813) through polymerase chain reaction cloning using degenerated primers based on a consensus CYP2 sequence and the heme-binding domain. This first CYP2K family member cloned from zebrafish had 1861 bp which contained 27 bp of 5'-untranslated region (5'-UTR), an open reading frame (ORF) of 1518 bp, and a 300 bp 3'-UTR with a poly A tail. The deduced 506 amino acid sequence of CYP2K6 had 63%, 62% and 59% identity with rainbow trout CYP2K1, CYP2K4 and CYP2K3, respectively; and 45%, 42%, and 42% identity with rabbit CYP2C1, human CYP2C19 and mouse CYP2C39, respectively. CYP2K6 mapped to 107.49cR on LG3 using the LN54 radiation hybrid panel. Its mRNA was detected at 5 days post-fertilization and in the adult liver and ovary among nine tissues examined. The ORF, including the 27 bp of the 5'-UTR, was cloned into pFastBac donor vector and then transferred into the baculovirus genome (bacmid DNA) in DH10Bac competent cells. The recombinant bacmid DNA was used to infect Spodoptera frugiperda insect cells to express the CYP2K6 protein (Bv-2K6). As its ortholog, rainbow trout Bv-2K1 [Yang, Y.H., Miranda, C.L., Henderson, M.C., Wang-Buhler, J.-L., Buhler, D.R., 2000. Heterologous expression of CYP2K1 and identification of the expressed protein (Bv-2K1) as lauric acid (omega-1)-hydroxylase and aflatoxin B1 exo-epoxidase. Drug Metab. Disp. 28,1279-83.], Bv-2K6 also catalyzed the conversion of aflatoxin B1 (AFB1) to its exo-8,9-epoxide as assessed by the trapping of a glutathione (GSH) adduct in the presence of a specific mouse alpha class glutathione S-transferase. The identity of the AFB1-GSH adduct was verified by liquid chromatography-mass spectrometry (LC-MS) and mass spectrometry-mass spectrometry (MS-MS) analysis. Although rainbow trout Bv-2K1 was capable of oxidizing lauric acid, zebrafish Bv-2K6 protein showed no activity against this substrate.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1532-0456
pubmed:author
pubmed:issnType
Print
pubmed:volume
140
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
207-19
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15907766-Aflatoxin B1, pubmed-meshheading:15907766-Alkane 1-Monooxygenase, pubmed-meshheading:15907766-Amino Acid Sequence, pubmed-meshheading:15907766-Animals, pubmed-meshheading:15907766-Aryl Hydrocarbon Hydroxylases, pubmed-meshheading:15907766-Baculoviridae, pubmed-meshheading:15907766-Base Sequence, pubmed-meshheading:15907766-Biotransformation, pubmed-meshheading:15907766-Chromatography, High Pressure Liquid, pubmed-meshheading:15907766-Chromatography, Liquid, pubmed-meshheading:15907766-Cloning, Molecular, pubmed-meshheading:15907766-Embryo, Nonmammalian, pubmed-meshheading:15907766-Fish Proteins, pubmed-meshheading:15907766-Gene Library, pubmed-meshheading:15907766-Mass Spectrometry, pubmed-meshheading:15907766-Molecular Sequence Data, pubmed-meshheading:15907766-Polymerase Chain Reaction, pubmed-meshheading:15907766-Recombinant Proteins, pubmed-meshheading:15907766-Sequence Alignment, pubmed-meshheading:15907766-Spodoptera, pubmed-meshheading:15907766-Steroid Hydroxylases, pubmed-meshheading:15907766-Tissue Distribution, pubmed-meshheading:15907766-Zebrafish
pubmed:year
2005
pubmed:articleTitle
CYP2K6 from zebrafish (Danio rerio): cloning, mapping, developmental/tissue expression, and aflatoxin B1 activation by baculovirus expressed enzyme.
pubmed:affiliation
Environmental and Molecular Toxicology, Environmental Health Sciences Center and Marine/Freshwater Biomedical Sciences Center, Oregon State University, Corvallis, OR 97331, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, N.I.H., Extramural