CARBON CATABOLITE REPRESSION CAN ACCOUNT FOR THE TEMPORAL PATTERN OF EXPRESSION OF A PENICILLIN BIOSYNTHETIC GENE IN ASPERGILLUS-NIDULANS

被引:77
作者
ESPESO, EA [1 ]
PENALVA, MA [1 ]
机构
[1] CSIC,CTR INVEST BIOL,VELAZQUEZ 144,E-28006 MADRID,SPAIN
关键词
D O I
10.1111/j.1365-2958.1992.tb00866.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aspergillus nidulans synthesizes penicillins as secondary metabolites when grown under certain culture conditions. Broths containing carbon (C) sources that give rise to carbon catabolite repression (CCR) support a much lower antibiotic yield than broths with non-repressing C sources. Steady-state levels of the isopenicillin N synthetase (IPNS) gene transcript are considerably reduced in mycelia grown with repressing C sources and are derepressed in mycelia grown with sugars which do not cause CCR, indicating that penicillin biosynthesis is regulated by CCR through transcriptional control of structural genes. CCR is sufficient to explain the temporal window of expression of the IPNS gene during the growth cycle since (i) the transcript becomes derepressed as soon as the concentration of a repressing C source drops to non-repressing levels and (ii) derepressing C sources sustain derepressed IPNS transcription at all tested moments of the growth cycle. Several tested hypofunctional mutations in creA (the negatively acting regulatory gene which mediates CCR in A. nidulans) do not cause full derepression of IPNS transcript in the presence of a repressing C source. The slight degree of IPNS derepression caused by some creA(d) (derepressed) alleles parallels the strength of the mutation (as determined by the morphological effect they elicit).
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页码:1457 / 1465
页数:9
相关论文
共 33 条
[1]  
[Anonymous], 2001, YEAST
[2]   NITROGEN METABOLITE REPRESSION IN ASPERGILLUS-NIDULANS [J].
ARST, HN ;
COVE, DJ .
MOLECULAR & GENERAL GENETICS, 1973, 126 (02) :111-141
[3]   AN INVERSION TRUNCATING THE CREA GENE OF ASPERGILLUS-NIDULANS RESULTS IN CARBON CATABOLITE DEREPRESSION [J].
ARST, HN ;
TOLLERVEY, D ;
DOWZER, CEA ;
KELLY, JM .
MOLECULAR MICROBIOLOGY, 1990, 4 (05) :851-854
[4]  
Arst HN, 1985, GENE MANIPULATIONS F, P309
[5]  
ARST HN, 1981, SOC GENERAL MICROBIO, V31, P131
[6]  
Arst Jr. HN, 1977, GENETICS PHYSL ASPER, P131
[7]   CARBON CATABOLITE REPRESSION IN ASPERGILLUS-NIDULANS [J].
BAILEY, C ;
ARST, HN .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1975, 51 (02) :573-577
[8]   CLONING AND CHARACTERIZATION OF THE ACYL-COENZYME-A-6-AMINOPENICILLANIC-ACID-ACYLTRANSFERASE GENE OF PENICILLIUM-CHRYSOGENUM [J].
BARREDO, JL ;
VANSOLINGEN, P ;
DIEZ, B ;
ALVAREZ, E ;
CANTORAL, JM ;
KATTEVILDER, A ;
SMAAL, EB ;
GROENEN, MAM ;
VEENSTRA, AE ;
MARTIN, JF .
GENE, 1989, 83 (02) :291-300
[9]   CLONING AND EXPRESSION OF THE ISOPENICILLIN-N SYNTHETASE GENE FROM PENICILLIUM-CHRYSOGENUM [J].
CARR, LG ;
SKATRUD, PL ;
SCHEETZ, ME ;
QUEENER, SW ;
INGOLIA, TD .
GENE, 1986, 48 (2-3) :257-266
[10]   A METHOD FOR ISOLATION OF INTACT, TRANSLATIONALLY ACTIVE RIBONUCLEIC-ACID [J].
CATHALA, G ;
SAVOURET, JF ;
MENDEZ, B ;
WEST, BL ;
KARIN, M ;
MARTIAL, JA ;
BAXTER, JD .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1983, 2 (04) :329-335