Cloning, characterisation, and heterologous expression of the Candida utilis malic enzyme gene View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-04

AUTHORS

M. Saayman, W. H. van Zyl, M. Viljoen-Bloom

ABSTRACT

The Candida utilis malic enzyme gene, CME1, was isolated from a cDNA library and characterised on a molecular and biochemical level. Sequence analysis revealed an open reading frame of 1,926 bp, encoding a 641 amino acid polypeptide with a predicted molecular weight of approximately 70.2 kDa. The inferred amino acid sequence suggested a cytosolic localisation for the malic enzyme, as well as 37 and 68% homologies with the malic enzymes of Schizosaccharomyces pombe and Saccharomyces cerevisiae, respectively. Expression of the CME1 gene was subject to carbon catabolite repression and substrate induction, similar to the regulatory mechanisms observed for the C. utilis dicarboxylic acid permease. The CME1 gene was successfully expressed in S. cerevisiae under control of the S. cerevisiae PGK1 promoter and terminator. When coexpressed with the S. pombe malate permease gene (mae1), it resulted in a recombinant S. cerevisiae strain able to completely degrade 90% of the extracellular L-malate within 24 h. More... »

PAGES

248-258

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00294-005-0052-z

DOI

http://dx.doi.org/10.1007/s00294-005-0052-z

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1003397844

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16437252


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