Literature DB >> 2064373

P450BM-3 and other inducible bacterial P450 cytochromes: biochemistry and regulation.

A J Fulco1.   

Abstract

When I began this review my goal was to present a coherent overview of the biochemistry and regulation of the inducible P450 cytochromes of bacteria. Now, at the end, I wonder if a unified perspective is possible at this time. On the basis of admittedly limited data, bacterial P450 systems seem as different from each other as they are, as a group, from the mammalian P450 cytochromes. The most obvious physical difference between the bacterial monooxygenases and their mammalian counterparts is solubility; with several possible exceptions (69, 70, 76), bacterial P450s are soluble whereas the microsomal and mitochondrial P450s are membrane-associated proteins. In structure and organization, however, the few well-characterized prokaryotic P450-dependent systems vary widely. The three-component arrangement is probably most common but even here variation is apparent. The P450cam putidaredoxin reductase contains only FAD and is quite specific for NADH (35, 39); the P450meg megaredoxin reductase contains only FMN and is specific for NADPH (59, 60). Putitive two-component P450 systems in bacteria have not yet been adequately characterized but the P450oct and P450npd monooxygenases (69, 70, 93) could well be organized in this way. The catalytically self-sufficient P450BM-3 is currently the only single-component P450-dependent monooxygenase known but additional examples of this arrangement may well be found in other bacteria. Paradoxically, P450BM-3 is structurally much more analogous to liver microsomal P450 systems than to any other bacterial P450 monooxygenase characterized to date. Another generally recognized difference between prokaryotic and eukaryotic P450s pertains to function; most known bacterial P450-dependent systems initiate the oxidation of recalcitrant carbon compounds so that the hosts can utilize them as sole carbon sources for growth. Some lower eukaryotes [certain yeasts, for example (134)] also employ P450-dependent systems in this way but, among most fungi as well as in higher eukaryotes, P450 cytochromes are involved in specific pathways of sterol or other lipid syntheses or, as in the mammalian liver microsomal systems, in detoxification reactions.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 2064373     DOI: 10.1146/annurev.pa.31.040191.001141

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  17 in total

1.  Brain nitric oxide synthase is a haemoprotein.

Authors:  P Klatt; K Schmidt; B Mayer
Journal:  Biochem J       Date:  1992-11-15       Impact factor: 3.857

Review 2.  Phenobarbital induction of cytochrome P-450 gene expression.

Authors:  D J Waxman; L Azaroff
Journal:  Biochem J       Date:  1992-02-01       Impact factor: 3.857

Review 3.  The other kind of biological NMR--studies of enzyme-substrate interactions.

Authors:  G C Roberts
Journal:  Neurochem Res       Date:  1996-09       Impact factor: 3.996

4.  A 53-base-pair inverted repeat negatively regulates expression of the adjacent and divergently oriented cytochrome P450(BM-1) gene and its regulatory gene, bm1P1, in Bacillus megaterium.

Authors:  G C Shaw; C C Sung; C H Liu; H S Kao
Journal:  J Bacteriol       Date:  1997-01       Impact factor: 3.490

5.  Fatty acid signals in Bacillus megaterium are attenuated by cytochrome P-450-mediated hydroxylation.

Authors:  N English; C N Palmer; W L Alworth; L Kang; V Hughes; C R Wolf
Journal:  Biochem J       Date:  1997-10-15       Impact factor: 3.857

6.  Benzoic acid 2-hydroxylase, a soluble oxygenase from tobacco, catalyzes salicylic acid biosynthesis.

Authors:  J León; V Shulaev; N Yalpani; M A Lawton; I Raskin
Journal:  Proc Natl Acad Sci U S A       Date:  1995-10-24       Impact factor: 11.205

Review 7.  In search of a function for tetrahydrobiopterin in the biosynthesis of nitric oxide.

Authors:  B Mayer; E R Werner
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1995-05       Impact factor: 3.000

8.  Exploring the electron transfer properties of neuronal nitric-oxide synthase by reversal of the FMN redox potential.

Authors:  Huiying Li; Aditi Das; Hiruy Sibhatu; Joumana Jamal; Stephen G Sligar; Thomas L Poulos
Journal:  J Biol Chem       Date:  2008-10-13       Impact factor: 5.157

9.  Effect of replacement of ferriprotoporphyrin IX in the haem domain of cytochrome P-450 BM-3 on substrate binding and catalytic activity.

Authors:  S Modi; W U Primrose; L Y Lian; G C Roberts
Journal:  Biochem J       Date:  1995-09-15       Impact factor: 3.857

10.  Cloning and expression of a member of a new cytochrome P-450 family: cytochrome P-450lin (CYP111) from Pseudomonas incognita.

Authors:  J D Ropp; I C Gunsalus; S G Sligar
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.