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Applied and Environmental Microbiology, December 2007, p. 7882-7890, Vol. 73, No. 24
0099-2240/07/$08.00+0     doi:10.1128/AEM.01097-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Anaerobic 1-Alkene Metabolism by the Alkane- and Alkene-Degrading Sulfate Reducer Desulfatibacillum aliphaticivorans Strain CV2803T{triangledown}

Vincent Grossi,1,2* Cristiana Cravo-Laureau,3 Alain Méou,4 Danielle Raphel,1 Frédéric Garzino,4 and Agnès Hirschler-Réa5

Laboratoire de Microbiologie, Géochimie et Ecologie Marines, Centre d'Océanologie de Marseille, UMR6117 CNRS, Faculté des Sciences de Luminy, case 901, 13288 Marseille cedex 09,1 Paléoenvironnements et Paléobiosphère, UMR5125 CNRS, Université Lyon 1, Campus de la Doua, Bâtiment Géode, 69622 Villeurbanne cedex,2 Equipe Environnement et Microbiologie, UMR5254 IPREM CNRS, IBEAS Université de Pau et des Pays de l'Adour, BP1155, 64013 Pau cedex,3 GCOM2, UMR6114 CNRS, Faculté des Sciences de Luminy, case 901, 13288 Marseille cedex 09,4 Laboratoire de Microbiologie et de Biotechnologie des Environnements Chauds, UMR_D 180, IRD, Universités de Provence et de la Méditerranée, case 925, 13288 Marseille cedex 09, France5

Received 16 May 2007/ Accepted 15 October 2007

The alkane- and alkene-degrading, marine sulfate-reducing bacterium Desulfatibacillum aliphaticivorans strain CV2803T, known to oxidize n-alkanes anaerobically by fumarate addition at C-2, was investigated for its 1-alkene metabolism. The total cellular fatty acids of this strain were predominantly C-(even number) (C-even) when it was grown on C-even 1-alkenes and predominantly C-(odd number) (C-odd) when it was grown on C-odd 1-alkenes. Detailed analyses of those fatty acids by gas chromatography-mass spectrometry after 6- to 10-week incubations allowed the identification of saturated 2- and 4-ethyl-, 2- and 4-methyl-, and monounsaturated 4-methyl-branched fatty acids with chain lengths that correlated with those of the 1-alkene. The growth of D. aliphaticivorans on (per)deuterated 1-alkenes provided direct evidence of the anaerobic transformation of these alkenes into the corresponding 1-alcohols and into linear as well as 10- and 4-methyl-branched fatty acids. Experiments performed with [13C]bicarbonate indicated that the initial activation of 1-alkene by the addition of inorganic carbon does not occur. These results demonstrate that D. aliphaticivorans metabolizes 1-alkene by the oxidation of the double bond at C-1 and by the subterminal addition of organic carbon at both ends of the molecule [C-2 and C-({omega}-1)]. The detection of ethyl-branched fatty acids from unlabeled 1-alkenes further suggests that carbon addition also occurs at C-3. Alkylsuccinates were not observed as potential initial intermediates in alkene metabolism. Based on our observations, the first pathways for anaerobic 1-alkene metabolism in an anaerobic bacterium are proposed. Those pathways indicate that diverse initial reactions of 1-alkene activation can occur simultaneously in the same strain of sulfate-reducing bacterium.


* Corresponding author. Mailing address: Paléoenvironnements et Paléobiosphère, UMR5125 PEPS CNRS, Université Lyon 1, Campus de la Doua, Bâtiment Géode, 69622 Villeurbanne Cedex, France. Phone: 33 472 445 813. Fax: 33 472 448 382. E-mail: vincent.grossi{at}univ-lyon1.fr

{triangledown} Published ahead of print on 26 October 2007.


Applied and Environmental Microbiology, December 2007, p. 7882-7890, Vol. 73, No. 24
0099-2240/07/$08.00+0     doi:10.1128/AEM.01097-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







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