Espeso E A, Peñalva M A
Centro de Investigaciones Biológicas del CSIC, Madrid, Spain.
Mol Microbiol. 1992 Jun;6(11):1457-65. doi: 10.1111/j.1365-2958.1992.tb00866.x.
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 depressed 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 creAd (derepressed) alleles parallels the strength of the mutation (as determined by the morphological effect they elicit).
构巢曲霉在特定培养条件下生长时会合成青霉素作为次级代谢产物。含有导致碳分解代谢物阻遏(CCR)的碳(C)源的发酵液所支持的抗生素产量远低于含有非阻遏性C源的发酵液。在使用阻遏性C源生长的菌丝体中,异青霉素N合成酶(IPNS)基因转录本的稳态水平显著降低,而在使用不会引起CCR的糖类生长的菌丝体中则受到抑制,这表明青霉素生物合成通过对结构基因的转录控制受CCR调节。CCR足以解释IPNS基因在生长周期中的表达时间窗口,因为(i)一旦阻遏性C源的浓度降至非阻遏水平,转录本就会去阻遏,并且(ii)在生长周期的所有测试时刻,去阻遏性C源都能维持IPNS转录的去阻遏状态。在creA(构巢曲霉中介导CCR的负向作用调节基因)中测试的几个功能减退突变,在存在阻遏性C源的情况下不会导致IPNS转录本完全去阻遏。一些creAd(去阻遏)等位基因引起的IPNS轻微去阻遏程度与突变强度平行(由它们引发的形态学效应确定)。