Please use this identifier to cite or link to this item:
http://hdl.handle.net/10362/63916| Title: | Molecular cloning and sequence analysis of the gene of the molybdenum‐containing aldehyde oxido‐reductase of Desulfovibrio gigas The deduced amino acid sequence shows similarity to xanthine dehydrogenase |
| Author: | Thoenes, Ulrich Flores, Orfeu L. Neves, Ana Devreese, Bart van Beeumen, Jozef J. Huber, Robert Romão, Maria J. LeGall, Jean Moura, José J.G. Rodrigues‐Pousada, Claudina |
| Keywords: | Biochemistry |
| Issue Date: | 1-Jan-1994 |
| Citation: | Thoenes, U., Flores, O. L., Neves, A., Devreese, B., van Beeumen, J. J., Huber, R., Romão, M. J., LeGall, J., Moura, J. J. G., & Rodrigues‐Pousada, C. (1994). Molecular cloning and sequence analysis of the gene of the molybdenum‐containing aldehyde oxido‐reductase of Desulfovibrio gigas The deduced amino acid sequence shows similarity to xanthine dehydrogenase. European Journal of Biochemistry, 220(3), 901-910. https://doi.org/10.1111/j.1432-1033.1994.tb18693.x |
| Abstract: | In this report, we describe the isolation of a 4020‐bp genomic PstI fragment of Desulfovibrio gigas harboring the aldehyde oxido‐reductase gene. The aldehyde oxido‐reductase gene spans 2718 bp of genomic DNA and codes for a protein with 906 residues. The protein sequence shows an average 52% (± 1.5%) similarity to xanthine dehydrogenase from different organisms. The codon usage of the aldehyde oxidoreductase is almost identical to a calculated codon usage of the Desulfovibrio bacteria. |
| Peer review: | yes |
| URI: | http://www.scopus.com/inward/record.url?scp=0028280650&partnerID=8YFLogxK |
| DOI: | https://doi.org/10.1111/j.1432-1033.1994.tb18693.x |
| ISSN: | 0014-2956 |
| Appears in Collections: | FCT: DQ - Artigos em revista internacional com arbitragem científica |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| THOENES_et_al_1994_European_Journal_of_Biochemistry.pdf | 1,6 MB | Adobe PDF | View/Open |
Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.











