THE PORCINE THROMBOXANE SYNTHASE-ENCODING CDNA - SEQUENCE MESSENGER-RNA EXPRESSION AND ENZYME-PRODUCTION IN SF9 INSECT CELLS

被引:16
作者
SHEN, RF
ZHANG, LQ
BAEK, SJ
TAI, HH
LEE, KD
机构
[1] UNIV MARYLAND, INST BIOTECHNOL, CTR MED BIOTECHNOL, BALTIMORE, MD 21201 USA
[2] UNIV KENTUCKY, COLL PHARM, LEXINGTON, KY 40506 USA
关键词
MOLECULAR CLONING; SEQUENCE COMPARISON; RECOMBINANT BACULOVIRUS;
D O I
10.1016/0378-1119(94)90555-X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A full-length cDNA encoding porcine thromboxane synthase (TS) was isolated and sequenced. The open reading frame encodes a 534-amino acid (aa) protein (M(r) 60451) which shares more than 75% identity with TS from other species and is 30% homologous to several enzymes of the cytochrome P-450 III family. Sequence comparison among porcine (p), human (h). and murine (m) TS indicated conservation of eight Cys residues and one putative N-glycosylation site. Several highly conserved regions were identified at the near N terminus, middle and C terminus. The most divergent region lies at aa residues 290-325, within which a Lys308 residue was unique to pTS. Between aa residues 70 and 90, considerable divergence was observed in mTS. Northern analysis showed that the pTS gene was expressed as a 2.3-kb transcript primarily in lung, kidney and thymus. A high-titer recombinant (re-) baculovirus containing pTS cDNA was developed to conduct a time course study of enzyme production in Spodoptera frugiperda (Sf9) cells. TS activity was detectable in the microsomes of Sf9 cells 12-h post-infection and reached maximum by 48 h. The produced TS resembles purified pTS in catalysis. as well as inhibition by a substrate analog inhibitor.
引用
收藏
页码:261 / 265
页数:5
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