This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Skory, C. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Skory, C. D.
Agricola
Right arrow Articles by Skory, C. D.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, June 2000, p. 2343-2348, Vol. 66, No. 6
0099-2240/00/$04.00+0

Isolation and Expression of Lactate Dehydrogenase Genes from Rhizopus oryzae

Christopher D. Skory*

Fermentation Biochemistry Research, National Center for Agricultural Utilization Research, Agricultural Research Service, U.S. Department of Agriculture, Peoria, Illinois 61604-3902

Received 15 July 1999/Accepted 31 January 2000

Rhizopus oryzae is used for industrial production of lactic acid, yet little is known about the genetics of this fungus. In this study I cloned two genes, ldhA and ldhB, which code for NAD+-dependent L-lactate dehydrogenases (LDH) (EC 1.1.1.27), from a lactic acid-producing strain of R. oryzae. These genes are similar to each other and exhibit more than 90% nucleotide sequence identity and they contain no introns. This is the first description of ldh genes in a fungus, and sequence comparisons revealed that these genes are distinct from previously isolated prokaryotic and eukaryotic ldh genes. Protein sequencing of the LDH isolated from R. oryzae during lactic acid production confirmed that ldhA codes for a 36-kDa protein that converts pyruvate to lactate. Production of LdhA was greatest when glucose was the carbon source, followed by xylose and trehalose; all of these sugars could be fermented to lactic acid. Transcripts from ldhB were not detected when R. oryzae was grown on any of these sugars but were present when R. oryzae was grown on glycerol, ethanol, and lactate. I hypothesize that ldhB encodes a second NAD+-dependent LDH that is capable of converting L-lactate to pyruvate and is produced by cultures grown on these nonfermentable substrates. Both ldhA and ldhB restored fermentative growth to Escherichia coli (ldhA pfl) mutants so that they grew anaerobically and produced lactic acid.


* Mailing address: NCAUR---USDA/ARS, 1815 N. University St., Peoria, IL 61604-3902. Phone: (309) 681-6275. Fax: (309) 681-6427. E-mail: skorycd{at}mail.ncaur.usda.gov.


Applied and Environmental Microbiology, June 2000, p. 2343-2348, Vol. 66, No. 6
0099-2240/00/$04.00+0



This article has been cited by other articles:

  • Abe, A., Oda, Y., Asano, K., Sone, T. (2007). Rhizopus delemar is the proper name for Rhizopus oryzae fumaric-malic acid producers.. Mycologia 99: 714-722 [Abstract] [Full Text]  
  • Kawaguchi, H., Vertes, A. A., Okino, S., Inui, M., Yukawa, H. (2006). Engineering of a Xylose Metabolic Pathway in Corynebacterium glutamicum.. Appl. Environ. Microbiol. 72: 3418-3428 [Abstract] [Full Text]  
  • Zhou, S., Shanmugam, K. T., Ingram, L. O. (2003). Functional Replacement of the Escherichia coliD-(-)-Lactate Dehydrogenase Gene (ldhA) with the L-(+)-Lactate Dehydrogenase Gene (ldhL) from Pediococcus acidilactici. Appl. Environ. Microbiol. 69: 2237-2244 [Abstract] [Full Text]  
  • Zhou, S., Causey, T. B., Hasona, A., Shanmugam, K. T., Ingram, L. O. (2003). Production of Optically Pure D-Lactic Acid in Mineral Salts Medium by Metabolically Engineered Escherichia coli W3110. Appl. Environ. Microbiol. 69: 399-407 [Abstract] [Full Text]