The induction of alpha-amylase by starch in Aspergillus oryzae: evidence for controlled mRNA expression
- PMID: 6208985
- DOI: 10.1139/o84-089
The induction of alpha-amylase by starch in Aspergillus oryzae: evidence for controlled mRNA expression
Abstract
The induction of alpha-amylase by starch has been studied in the filamentous fungus Aspergillus oryzae. Low levels of alpha-amylase activity were found in both intracellular and extracellular samples from glucose-grown cultures. However, alpha-amylase activity increased when starch was the sole carbon source. The intracellular enzyme activity was induced by a factor of approximately 6.5, while the extracellular activity increased 20-fold over that found in the glucose-grown cultures. Regardless of the carbon source or cellular location, the molecular weight of the active protein was 52 500 +/- 1800 and only this protein reacted with antibodies specific for alpha-amylase. A parallel study of the in vitro translated proteins directed by poly(A)+ RNA fractions indicated a presumptive alpha-amylase with a similar isoelectric point but with a molecular weight of approximately 54 000. This protein was most prevalent using RNA from early, exponentially growing cultures in starch medium. Immunoprecipitation data indicate that the abundance of alpha-amylase transcripts decreases dramatically after the first 12 h, reflecting an initial transcription control for the expression of this enzyme.
Similar articles
-
Physiological characterisation of recombinant Aspergillus nidulans strains with different creA genotypes expressing A. oryzae alpha-amylase.J Biotechnol. 2002 Jan 18;92(3):279-85. doi: 10.1016/s0168-1656(01)00366-2. J Biotechnol. 2002. PMID: 11689252
-
[Regulation of alpha-amylase biosynthesis in an Aspergillus oryzae 3000 strain based on the principle of feedback from the level of the active enzyme].Acta Microbiol Bulg. 1983;13:91-7. Acta Microbiol Bulg. 1983. PMID: 6606299 Bulgarian. No abstract available.
-
Some studies of alpha-amylase production using Aspergillus oryzae.Pak J Biol Sci. 2008 Nov 15;11(22):2553-9. doi: 10.3923/pjbs.2008.2553.2559. Pak J Biol Sci. 2008. PMID: 19260332
-
Taka-amylase A in the conidia of Aspergillus oryzae RIB40.Biosci Biotechnol Biochem. 2005 Nov;69(11):2035-41. doi: 10.1271/bbb.69.2035. Biosci Biotechnol Biochem. 2005. PMID: 16306682 Review.
-
Evolutionary Trends in Industrial Production of α-amylase.Recent Pat Biotechnol. 2019;13(1):4-18. doi: 10.2174/2211550107666180816093436. Recent Pat Biotechnol. 2019. PMID: 30810102 Review.
Cited by
-
Expression and regulation of glucoamylase from the yeast Schwanniomyces castellii.J Bacteriol. 1990 May;172(5):2360-6. doi: 10.1128/jb.172.5.2360-2366.1990. J Bacteriol. 1990. PMID: 2110140 Free PMC article.
-
Aspergillus nidulans nuclear proteins bind to a CCAAT element and the adjacent upstream sequence in the promoter region of the starch-inducible Taka-amylase A gene.Mol Gen Genet. 1993 Feb;237(1-2):251-60. doi: 10.1007/BF00282807. Mol Gen Genet. 1993. PMID: 8455560
-
β-galactosidase Production by Aspergillus niger ATCC 9142 Using Inexpensive Substrates in Solid-State Fermentation: Optimization by Orthogonal Arrays Design.Iran Biomed J. 2016;20(5):287-294. doi: 10.22045/ibj.2016.06. Epub 2016 May 25. Iran Biomed J. 2016. PMID: 27721510 Free PMC article.
-
Construction of a fusion gene comprising the Taka-amylase A promoter and the Escherichia coli beta-glucuronidase gene and analysis of its expression in Aspergillus oryzae.Mol Gen Genet. 1991 Oct;229(2):301-6. doi: 10.1007/BF00272170. Mol Gen Genet. 1991. PMID: 1921978
-
Cloning and expression of a Saccharomyces diastaticus glucoamylase gene in Saccharomyces cerevisiae and Schizosaccharomyces pombe.J Bacteriol. 1986 May;166(2):484-90. doi: 10.1128/jb.166.2.484-490.1986. J Bacteriol. 1986. PMID: 3009402 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources