MOLECULAR-CLONING AND FUNCTIONAL EXPRESSION OF A TALAROMYCES-EMERSONII DERIVED ALPHA-AMYLASE ENCODING GENETIC DETERMINANT IN A HUMAN CELL-LINE

被引:1
作者
BUNNI, L
HACKETT, TJ
MCHALE, L
FLYNN, G
MCHALE, AP
机构
[1] UNIV DUBLIN TRINITY COLL,DEPT MICROBIOL,DUBLIN 2,IRELAND
[2] ARTHUR ANDERSON CONSULTING,LONDON,ENGLAND
关键词
D O I
10.1007/BF00131196
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A cDNA fragment encoding a Talaromyces emersonii acid stable alpha-amylase has, been cloned into a mammalian cell expression vector system. When human HeLa cells were transformed with this DNA, functional enzyme could be detected in extracellular media and cell lysates derived from stable transformants. Expression of the T. emersonii derived cDNA was verified by northern dot blotting hybridisation analysis of mRNA extracted from transformants, using the labelled amylase encoding cDNA determinant as a probe. Results obtained suggest that expression of the fungus derived alpha-amylase in the transformed HeLa cells is glucocorticoid dependent.
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页码:1095 / 1100
页数:6
相关论文
共 13 条
[1]   PRODUCTION, ISOLATION AND PARTIAL CHARACTERIZATION OF AN AMYLASE SYSTEM PRODUCED BY TALAROMYCES-EMERSONII CBS-814.70 [J].
BUNNI, L ;
MCHALE, L ;
MCHALE, AP .
ENZYME AND MICROBIAL TECHNOLOGY, 1989, 11 (06) :370-375
[2]  
BUNNI L, 1989, Biotechnology Techniques, V3, P107, DOI 10.1007/BF01875562
[3]  
BUNNI L, 1992, IN PRESS BIOTECH LET
[4]  
CHEN CA, 1988, BIOTECHNIQUES, V6, P632
[5]   MODIFICATION OF HUMAN SALIVARY AMYLASE USING DEXTRAN-T-70 [J].
DONLAN, B ;
MCHALE, ML ;
MCHALE, AP .
BIOTECHNOLOGY LETTERS, 1988, 10 (08) :559-562
[6]  
JONES B, 1989, Biotechnology Techniques, V3, P355, DOI 10.1007/BF01875636
[7]   GLUCOCORTICOIDS REGULATE EXPRESSION OF DIHYDROFOLATE-REDUCTASE CDNA IN MOUSE MAMMARY-TUMOR VIRUS CHIMAERIC PLASMIDS [J].
LEE, F ;
MULLIGAN, R ;
BERG, P ;
RINGOLD, G .
NATURE, 1981, 294 (5838) :228-232
[8]  
LOTT JA, 1991, ANAL CHEM, V63, P102
[9]  
Maniatis T., 1982, MOL CLONING
[10]  
MCCARTHY U, 1988, BIOCHEM SOC T, V17, P393