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Expression profile of amylolytic genes in Aspergillus nidulans.

Bioscience, biotechnology, and biochemistry (2006-10-13)
Takashi Nakamura, Yuki Maeda, Nami Tanoue, Tomohiro Makita, Masashi Kato, Tetsuo Kobayashi
RESUMEN

Aspergillus nidulans possessed 16 putative amylolytic genes consisting of 7 alpha-glucosidase (agdA-F), 7 alpha-amylase (amyA-F), and 2 glucoamylase (glaA and B) genes on the genome. Among them, the agdA, agdB, agdE, agdF, amyA, amyB, amyF, and glaB genes were induced by isomaltose. AmyR, a Zn(II)(2)Cys(6) transcription factor, was required for the induction. The isomaltose-inducible genes possessed at least one consensus sequence for AmyR binding, 5'-CGGN(8)CGG, on each promoter region. None of the amylolytic genes was induced by maltose. The mRNA levels of the amylolytic genes except for agdC, amyD, and amyG increased under carbon-starved conditions. Release from CreA-dependent carbon catabolite repression was the main cause of the increase, but, the mRNA levels of agdB, agdF, amyB, amyF, and glaB increased to some extent even in a creA mutant. Therefore, both CreA-dependent and -independent mechanisms are involved in the up-regulation of the amylolytic genes under carbon-starved conditions.

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Sigma-Aldrich
Creatinase from microorganisms, lyophilized powder, ≥4 units/mg solid
Sigma-Aldrich
Creatinase from Pseudomonas sp., recombinant, expressed in E. coli, lyophilized powder, 10-15 units/mg protein