Phylogenetic analysis reveals the surprising diversity of an oxygenase class

被引:19
作者
Capyk, Jenna K. [2 ]
Eltis, Lindsay D. [1 ,2 ]
机构
[1] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
来源
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY | 2012年 / 17卷 / 03期
关键词
Rieske oxygenase; Enzyme family; Phylogenetic analysis; Enzyme classification; Structure-based sequence alignment; RING-HYDROXYLATING DIOXYGENASE; CRYSTAL-STRUCTURE; NAPHTHALENE 1,2-DIOXYGENASE; SEQUENCE ALIGNMENT; RIESKE OXYGENASE; CARBAZOLE 1,9A-DIOXYGENASE; COMPONENT; IRON; PROTEIN; DEGRADATION;
D O I
10.1007/s00775-011-0865-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As metalloenzymes capable of transforming a broad range of substrates with high stereo- and regiospecificity, the multicomponent Rieske oxygenases (ROs) have been studied in bacterial systems for applications in bioremediation and industrial biocatalysis. These studies include genetic and biochemical investigations, determination of enzyme structure, phylogenetic analysis, and enzyme classification. Although RO terminal oxygenase components (RO-Os) share a conserved domain structure, their sequences are highly divergent and present significant challenges for identification and classification. Herein, we present the first global phylogenetic analysis of a broad range of RO-Os from diverse taxonomic groups. We employed objective, structure-based criteria to significantly reduce the inclusion of erroneously aligned sequences in the analysis. Our findings reveal that RO biochemical studies to date have been largely concentrated in an unexpectedly narrow portion of the RO-O sequence landscape. Additionally, our analysis demonstrates the existence two distinct groups of RO-O sequences. Finally, the sequence diversity recognized in this study necessitates a new RO-O classification scheme. We therefore propose a P450-like naming system. Our results reveal a diversity of sequence and potential catalytic functionality that has been wholly unappreciated in the RO literature. This study also demonstrates that many commonly used bioinformatic tools may not be sufficient to analyze the vast amount of data available in current databases. These findings facilitate the expanded exploration of RO catalytic capabilities in both biological and technological contexts and increase the potential for practical exploitation of their activities.
引用
收藏
页码:425 / 436
页数:12
相关论文
共 50 条
[1]  
Ballou D, 1988, Prog Clin Biol Res, V274, P211
[2]  
Batie CJ., 1991, CHEM BIOCH FLAVOENZY, P543
[3]   Arene cis-dihydrodiol formation:: from biology to application [J].
Boyd, DR ;
Bugg, TDH .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2006, 4 (02) :181-192
[4]   Mycobacterial Cytochrome P450 125 (Cyp125) Catalyzes the Terminal Hydroxylation of C27 Steroids [J].
Capyk, Jenna K. ;
Kalscheuer, Rainer ;
Stewart, Gordon R. ;
Liu, Jie ;
Kwon, Hyukin ;
Zhao, Rafael ;
Okamoto, Sachi ;
Jacobs, William R., Jr. ;
Eltis, Lindsay D. ;
Mohn, William W. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (51) :35534-35542
[5]   Characterization of 3-Ketosteroid 9α-Hydroxylase, a Rieske Oxygenase in the Cholesterol Degradation Pathway of Mycobacterium tuberculosis [J].
Capyk, Jenna K. ;
D'Angelo, Igor ;
Strynadka, Natalie C. ;
Eltis, Lindsay D. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (15) :9937-9946
[6]   Crystal structure of the terminal oxygenase component of cumene dioxygenase from Pseudomonas fluorescens IP01 [J].
Dong, XS ;
Fushinobu, S ;
Fukuda, E ;
Terada, T ;
Nakamura, S ;
Shimizu, K ;
Nojiri, H ;
Omori, T ;
Shoun, H ;
Wakagi, T .
JOURNAL OF BACTERIOLOGY, 2005, 187 (07) :2483-2490
[7]  
Drummond A. J., 2010, GENEIOUS VERSION 5 5
[8]   Crystal Structure of Dicamba Monooxygenase: A Rieske Nonheme Oxygenase that Catalyzes Oxidative Demethylation [J].
Dumitru, Razvan ;
Jiang, Wen Zhi ;
Weeks, Donald P. ;
Wilson, Mark A. .
JOURNAL OF MOLECULAR BIOLOGY, 2009, 392 (02) :498-510
[9]   MUSCLE: multiple sequence alignment with high accuracy and high throughput [J].
Edgar, RC .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :1792-1797
[10]  
Felsenstein J, 1989, CLADISTICS, V5, P164