Literature DB >> 241011

Fatty acid hydroxylation in rat kidney cortex microsomes.

A Ellin, S Orrenius.   

Abstract

Rat kidney microsomes have been found to catalyze the hydroxylation of medium-chained fatty acids to the omega- and (omego-1)-hydroxy derivatives. This reaction, which requires NADPH and molecular oxygen, is a function of monooxygenase system present in the kidney microsomes, containing NADPH-cytochrome c reductase and cytochrome P-450K. NADH is about half as effective as an electron donor as NADPH and there is an additive effect in the presence of both nucleotides. Cytochrome P-450K absorbs light maximally at 452-3 nm, when it is reduced and bound to carbon monoxide. The extinction coefficient of this complex is 91 mM(-1) cm(-1). Electrons from NADPH are transferred to cytochrome P-450K via the NADPH-cytochrome c reductase. The reduction rate of cytochrome P-450K is stimulated by added fatty acids and the reduction kinetics reveal the presence of endogenous substrates bound to cytochrome P-450K. Both cytochrome P-450K concentration and fatty acid hydroxylation activity in kidney microsomes are increased by starvation. On the other hand, phenobarbital treatment of the rats has no effect on either the hemoprotein or the overall hydroxylation reaction and 3,4-benzpyrene administration induces a new species of cytochrome P-450K not involved in fatty acid hydroxylation. Cytochrome P-450K shows, in contrast to liver P-450, high substrate specificity. The only substances forming enzyme-substrate complexes with cytochrome P-450K are the medium-chained fatty acids and certain derivatives of these acids. The chemical requirements for substrate binding include a carbon chain of medium length and at the end of the chain a carbonyl group and a free electron pair on a neighbouring atom. The distance between the binding site for the carbonyl group and the active oxygen is suggested to be in the order of 16 A. This distance fixes the ratio of omega- and (omega-1)-hydroxylated products formed from a certain fatty acid by the single species of cytochrome P-450K involved. The membrane microenvironment seems also to be of importance for the substrate specificity of cytochrome P-450K, since removal of the cytochrome from the membrane lowers its binding specificity to some extent. A comparison between the liver and kidney cytochrome P-450 systems suggests that the kidney cytochrome P-450K system is specialized for fatty acid hydroxylation.

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Year:  1975        PMID: 241011     DOI: 10.1007/bf02116235

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  37 in total

1.  Researches on fat metabolism. II.

Authors:  P E Verkade; J Van Der Lee
Journal:  Biochem J       Date:  1934       Impact factor: 3.857

2.  Preparation of antisera against cytochrome b 5 and NADPH-cytochrome c reductase from rat liver microsomes.

Authors:  M Raftell; S Orrenius
Journal:  Biochim Biophys Acta       Date:  1971-04-13

3.  Studies on the kinetics of cytochrome P-450 reduction in rat liver microsomes.

Authors:  H Diehl; J Schädelin; V Ullrich
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1970-11

4.  Studies on cytochrome P-450 of rat kidney cortex microsomes.

Authors:  A Ellin; S Orrenius
Journal:  Chem Biol Interact       Date:  1971-08       Impact factor: 5.192

5.  A new method for simultaneous purification of cytochrome b5 and NADPH-cytochrome c reductase from rat liver microsomes.

Authors:  T Omura; S Takesue
Journal:  J Biochem       Date:  1970-02       Impact factor: 3.387

6.  Mechanism of inhibition of microsomal mixed-function oxidation by the gut-contents inhibitor of the southern armyworm (Prodenia eridania).

Authors:  S Orrenius; M Berggren; P Moldéus; R I Krieger
Journal:  Biochem J       Date:  1971-09       Impact factor: 3.857

7.  On the fatty acid and hydrocarbon hydroxylation in rat liver microsomes.

Authors:  M L Das; S Orrenius; L Ernster
Journal:  Eur J Biochem       Date:  1968-05

8.  Possible role of P-450 in the oxidation of drugs in liver microsomes.

Authors:  R Kato
Journal:  J Biochem       Date:  1966-06       Impact factor: 3.387

9.  The nature of the reverse type I (modified type II) spectral change in liver microsomes.

Authors:  J B Schenkman; D L Cinti; S Orrenius; P Moldeus; R Kraschnitz
Journal:  Biochemistry       Date:  1972-11-07       Impact factor: 3.162

10.  -Oxidation of fatty acids. I. Mechanism of microsomal 1- and 2-hydroxylation.

Authors:  M Hamberg; I Björkhem
Journal:  J Biol Chem       Date:  1971-12-25       Impact factor: 5.157

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  3 in total

1.  Cytochrome p-450-dependent hydroxylation of lauric Acid at the subterminal position and oxidation of unsaturated analogs in wheat microsomes.

Authors:  A Zimmerlin; J P Salaün; F Durst; C Mioskowski
Journal:  Plant Physiol       Date:  1992-10       Impact factor: 8.340

Review 2.  The renal cytochrome P-450 arachidonic acid system.

Authors:  M Laniado-Schwartzman; N G Abraham
Journal:  Pediatr Nephrol       Date:  1992-09       Impact factor: 3.714

3.  Metabolism of arachidonate through NADPH-dependent oxygenase of renal cortex.

Authors:  A R Morrison; N Pascoe
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

  3 in total

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