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  4. Candida yeast long chain fatty alcohol oxidase is a c-type haemoprotein and plays an important role in long chain fatty acid metabolism
 
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Titre

Candida yeast long chain fatty alcohol oxidase is a c-type haemoprotein and plays an important role in long chain fatty acid metabolism

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids  
Auteur(s)
Cheng, Q.
Auteure/Auteur
Sanglard, D.
Auteure/Auteur
Vanhanen, S.
Auteure/Auteur
Liu, H. T.
Auteure/Auteur
Bombelli, P.
Auteure/Auteur
Smith, A.
Auteure/Auteur
Slabas, A. R.
Auteure/Auteur
Liens vers les personnes
Sanglard, Dominique  
Liens vers les unités
Institut universitaire de microbiologie  
ISSN
1388-1981
Statut éditorial
Publié
Date de publication
2005-08
Volume
1735
Numéro
3
Première page
192
Dernière page/numéro d’article
203
Peer-reviewed
Oui
Notes
Journal Article Research Support, Non-U.S. Gov't --- Old month value: Aug 15
Résumé
The industrial yeasts Candida tropicalis or Candida cloacae are able to grow on a variety of long chain alkanes and fatty acids as the sole carbon source. The complete oxidation of these substrates involves two sequential oxidative pathways: omega-oxidation, comprising the P450 alkane oxidase, a flavin-dependent membrane-bound long chain fatty alcohol oxidase [FAO] and a possible separate aldehyde oxidase [F.M. Dickinson, C. Wadforth, Purification and some properties of alcohol oxidase from alkane-grown Candida tropicalis, Biochem. J. 282 (1992) 325-331], and the beta-oxidation pathway, which utilises acylCoA substrates. We recently purified the membrane-bound long chain fatty alcohol oxidase FAO1 and confirmed it is also a c-type haemoprotein. Multiple isoforms may exist for many of these long chain fatty alcohol oxidases and the in vivo requirements for individual genes with respect to specific substrates are still being elucidated. In vitro reconstitution experiments have demonstrated that in Candida maltosa, the cytochrome P450 52A3 gene product can completely oxidise alkanes to dicarboxylic acids [U. Scheller, T. Zimmer, D. Becher, F. Schauer, W. Schunck, Oxygenation Cascade in Conversion of n-Alkanes to, -Dioic Acids Catalyzed by Cytochrome P450 52A3, J. Biol. Chem. 273 (1998) 32528-32534], potentially obviating requirements for a long chain alcohol oxidase. Here, we directly determine in vivo the role of the long chain alcohol oxidase (FAOT) in C. tropicalis, grown on a variety of substrates, followed by gene deletion. The faot double knockout has no detectable faot activity and is incapable of growth on octadecane, but it grows well on oleic acid, palmitic acid and shorter chain alkanes/fatty acids. A spontaneous mutation[s] may have occurred in the faot double gene knockout of C. tropicalis resulting in its inability to grow on oleic acid and hexadecane. The mutations demonstrate that different pathways of octadecane, hexadecane, oleic acid and palmitic acid utilisation exist in C. tropicalis.
Sujets

Alcohol Oxidoreductas...

PID Serval
serval:BIB_C5330022BA7E
DOI
10.1016/j.bbalip.2005.06.006
PMID
16046182
WOS
000231413500005
Permalien
https://iris.unil.ch/handle/iris/228838
Date de création
2008-01-25T13:40:42.305Z
Date de création dans IRIS
2025-05-21T04:55:36Z
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