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 Google Scholar
Google Scholar
Right arrow Articles by Park, M.
Right arrow Articles by Jeon, C. O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Park, M.
Right arrow Articles by Jeon, C. O.
Agricola
Right arrow Articles by Park, M.
Right arrow Articles by Jeon, C. O.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, August 2007, p. 5146-5152, Vol. 73, No. 16
0099-2240/07/$08.00+0     doi:10.1128/AEM.00782-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Molecular and Biochemical Characterization of 3-Hydroxybenzoate 6-Hydroxylase from Polaromonas naphthalenivorans CJ2{triangledown}

Minjeong Park,1 Yeji Jeon,1 Ho Hee Jang,1 Hyun-Su Ro,2 Woojun Park,3 Eugene L. Madsen,4 and Che Ok Jeon1*

Division of Applied Life Science, EB-NCRC, PMBBRC,1 Department of Microbiology, Gyeongsang National University, Jinju 660-701,2 Division of Environmental Science and Ecological Engineering, Korea University, Seoul 136-701, Republic of Korea,3 Department of Microbiology, Cornell University, Ithaca, New York 14853-81014

Received 8 April 2007/ Accepted 8 June 2007

Prior research revealed that Polaromonas naphthalenivorans CJ2 carries and expresses genes encoding the gentisate metabolic pathway for naphthalene. These metabolic genes are split into two clusters, comprising nagRAaGHAbAcAdBFCQEDJI'-orf1-tnpA and nagR2-orf2I''KL (C. O. Jeon, M. Park, H. Ro, W. Park, and E. L. Madsen, Appl. Environ. Microbiol. 72:1086-1095, 2006). BLAST homology searches of sequences in GenBank indicated that the orf2 gene from the small cluster likely encoded a salicylate 5-hydroxylase, presumed to catalyze the conversion of salicylate into gentisate. Here, we report physiological and genetic evidence that orf2 does not encode salicylate 5-hydroxylase. Instead, we have found that orf2 encodes 3-hydroxybenzoate 6-hydroxylase, the enzyme which catalyzes the NADH-dependent conversion of 3-hydroxybenzoate into gentisate. Accordingly, we have renamed orf2 nagX. After expression in Escherichia coli, the NagX enzyme had an approximate molecular mass of 43 kDa, as estimated by gel filtration, and was probably a monomeric protein. The enzyme was able to convert 3-hydroxybenzoate into gentisate without salicylate 5-hydroxylase activity. Like other 3-hydroxybenzoate 6-hydroxylases, NagX utilized both NADH and NADPH as electron donors and exhibited a yellowish color, indicative of a bound flavin adenine dinucleotide. An engineered mutant of P. naphthalenivorans CJ2 defective in nagX failed to grow on 3-hydroxybenzoate but grew normally on naphthalene. These results indicate that the previously described small catabolic cluster in strain CJ2 may be multifunctional and is essential for the degradation of 3-hydroxybenzoate. Because nagX and an adjacent MarR-type regulatory gene are both closely related to homologues in Azoarcus species, this study raises questions about horizontal gene transfer events that contribute to operon evolution.


* Corresponding author. Mailing address: Division of Applied Life Science, EB-NCRC, PMBBRC, Gyeongsang National University, Jinju 660-701, Republic of Korea. Phone: 82 55 751 6252. Fax: 82 55 759 9363. E-mail: cojeon{at}gnu.ac.kr

{triangledown} Published ahead of print on 22 June 2007.


Applied and Environmental Microbiology, August 2007, p. 5146-5152, Vol. 73, No. 16
0099-2240/07/$08.00+0     doi:10.1128/AEM.00782-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.