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Appl Environ Microbiol, March 1998, p. 843-849, Vol. 64, No. 3
Lehrstuhl für Mikrobiologie,
Universität München, D-80638 Munich, Federal Republic of
Germany
Received 21 May 1997/Accepted 21 November 1997
The
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Regulation of the Aspergillus nidulans
Penicillin Biosynthesis Gene acvA (pcbAB) by
Amino Acids: Implication for Involvement of Transcription Factor
PACC
-lactam antibiotic penicillin is produced as an end product
by some filamentous fungi only. It is synthesized from the amino acid
precursors L-
-aminoadipic acid, L-cysteine,
and L-valine. Previous data suggested that certain amino
acids play a role in the regulation of its biosynthesis. Therefore, in
this study the effects of externally added amino acids on both
Aspergillus (Emericella) nidulans
penicillin production and expression of the bidirectionally oriented
biosynthesis genes acvA (pcbAB) and
ipnA (pcbC) were comprehensively investigated.
Different effects caused by amino acids on the expression of penicillin
biosynthesis genes and penicillin production were observed. Amino acids
with a major negative effect on the expression of acvA-uidA
and ipnA-lacZ gene fusions, i.e., histidine, valine,
lysine, and methionine, led to a decreased ambient pH during
cultivation of the fungus. An analysis of deletion clones lacking
binding sites for the pH-dependent transcriptional factor PACC in the
intergenic regions between acvA-uidA and
ipnA-lacZ gene fusions and in a pacC5 mutant
(PacC5-5) suggested that the negative effects of histidine and valine
on acvA-uidA expression were due to reduced activation by
PACC under acidic conditions. These data also implied that PACC
regulates the expression of acvA, predominantly through
PACC binding site ipnA3. The repressing effect caused by lysine and
methionine on acvA expression, however, was even enhanced
in one of the deletion clones and the pacC5 mutant strain,
suggesting that regulators other than PACC are also involved.
*
Corresponding author. Mailing address: Lehrstuhl
für Mikrobiologie, Universität München,
Maria-Ward-Straße 1a, D-80638 Munich, Federal Republic of Germany.
Phone: 49 89 17919867. Fax: 49 89 17919862. E-mail:
A.Brakhage{at}lrz.uni-muenchen.de.
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