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 Galkin, A.
Right arrow Articles by Esaki, N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Galkin, A.
Right arrow Articles by Esaki, N.
Agricola
Right arrow Articles by Galkin, A.
Right arrow Articles by Esaki, N.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, September 1999, p. 4014-4020, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Cold-Adapted Alanine Dehydrogenases from Two Antarctic Bacterial Strains: Gene Cloning, Protein Characterization, and Comparison with Mesophilic and Thermophilic Counterparts

Andrey Galkin,1 Ljudmila Kulakova,1 Hiroyuki Ashida,2 Yoshihiro Sawa,2 and Nobuyoshi Esaki1,*

Institute for Chemical Research, Kyoto University, Uji, Kyoto-Fu 611,1 and Department of Applied Biochemistry, Faculty of Agriculture, Shimane University, Matsue,2 Japan

Received 8 March 1999/Accepted 28 June 1999

The genes encoding NAD+-dependent alanine dehydrogenases (AlaDHs) (EC 1.4.1.1) from the Antarctic bacterial organisms Shewanella sp. strain Ac10 (SheAlaDH) and Carnobacterium sp. strain St2 (CarAlaDH) were cloned and expressed in Escherichia coli. Of all of the AlaDHs that have been sequenced, SheAlaDH exhibited the highest level of sequence similarity to the AlaDH from the gram-negative bacterium Vibrio proteolyticus (VprAlaDH). CarAlaDH was most similar to AlaDHs from mesophilic and thermophilic Bacillus strains. SheAlaDH and CarAlaDH had features typical of cold-adapted enzymes; both the optimal temperature for catalytic activity and the temperature limit for retaining thermostability were lower than the values obtained for the mesophilic counterparts. The kcat/Km value for the SheAlaDH reaction was about three times higher than the kcat/Km value for VprAlaDH, but it was much lower than the kcat/Km value for the AlaDH from Bacillus subtilis. Homology-based structural models of various AlaDHs, including the two psychrotrophic AlaDHs, were constructed. The thermal instability of SheAlaDH and CarAlaDH may result from relatively low numbers of salt bridges in these proteins.


* Corresponding author. Mailing address: Institute for Chemical Research, Kyoto University, Uji, Kyoto-Fu 611-0011, Japan. Phone: 81-774-38-3240. Fax: 81-774-38-3248. E-mail: esaki{at}scl.kyoto-u.ac.jp.


Applied and Environmental Microbiology, September 1999, p. 4014-4020, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Kawamoto, J., Kurihara, T., Yamamoto, K., Nagayasu, M., Tani, Y., Mihara, H., Hosokawa, M., Baba, T., Sato, S. B., Esaki, N. (2009). Eicosapentaenoic Acid Plays a Beneficial Role in Membrane Organization and Cell Division of a Cold-Adapted Bacterium, Shewanella livingstonensis Ac10. J. Bacteriol. 191: 632-640 [Abstract] [Full Text]  
  • Schroder, I., Vadas, A., Johnson, E., Lim, S., Monbouquette, H. G. (2004). A Novel Archaeal Alanine Dehydrogenase Homologous to Ornithine Cyclodeaminase and {micro}-Crystallin. J. Bacteriol. 186: 7680-7689 [Abstract] [Full Text]  
  • Orikoshi, H., Baba, N., Nakayama, S., Kashu, H., Miyamoto, K., Yasuda, M., Inamori, Y., Tsujibo, H. (2003). Molecular Analysis of the Gene Encoding a Novel Cold-Adapted Chitinase (ChiB) from a Marine Bacterium, Alteromonas sp. Strain O-7. J. Bacteriol. 185: 1153-1160 [Abstract] [Full Text]  
  • Lonhienne, T., Mavromatis, K., Vorgias, C. E., Buchon, L., Gerday, C., Bouriotis, V. (2001). Cloning, Sequences, and Characterization of Two Chitinase Genes from the Antarctic Arthrobacter sp. Strain TAD20: Isolation and Partial Characterization of the Enzymes. J. Bacteriol. 183: 1773-1779 [Abstract] [Full Text]