A taxonomic study was carried out on strain P24 T , which was isolated from a polycyclic aromatic hydrocarbon-degrading consortium, enriched from a deep-seawater sample collected from the Indian Ocean. The isolate was Gram-negative, rod-shaped, motile by means of a polar flagellum, moderately halophilic and capable of reducing nitrate to nitrite. Growth was observed at salinities of 0-9 % and at temperatures of 10-42 6C. The strain was unable to degrade Tween 80 or gelatin. The dominant fatty acids were C 16 : 0 (15.2 % of the total), C 18 : 0 (10.3 %), C 18 : 1 v7c (52.0 %), C 18 : 1 2-OH (4.7 %) and C 19 : 0 v8c cyclo (4.7 %). The G+C content of the chromosomal DNA was 64.8 mol%. 16S rRNA gene sequence comparisons showed that strain P24 T was related most closely to Thalassobaculum litoreum CL-GR58 T (92.7 % similarity); levels of similarity between strain P24 T and type strains of recognized species in the family Rhodospirillaceae were all less than 90.8 %. Phylogenetic analyses based on 16S rRNA gene sequences showed that strain P24 T formed a distinct evolutionary lineage within the family Rhodospirillaceae. Strain P24 T could be distinguished from phylogenetically related genera based on differences in several phenotypic properties. On the basis of the phenotypic and phylogenetic data presented, strain P24 T is considered to represent a novel species of a new genus, for which the name Oceanibaculum indicum gen. nov., sp. nov. is proposed. The type strain is P24 T (5CCTCC AB 208226 T 5LMG 24626 T 5MCCC 1A02083 T ).To investigate polycyclic aromatic hydrocarbon (PAH)-degrading bacteria from deep seawater of the Indian Ocean, many bacterial strains were isolated and characterized taxonomically. The present study focuses on one of these isolates, designated strain P24 T . Comparative 16S rRNA gene sequence analysis indicated that strain P24 T formed a deep branch within the family Rhodospirillaceae. Accordingly, the aim was to determine the exact taxonomic position of strain P24 T by using a polyphasic characterization, including determination of phenotypic properties and detailed phylogenetic analysis based on 16S rRNA gene sequences. Enrichment was undertaken on board immediately after sampling. Two months later, at our laboratory, 1 ml of the enrichment culture was transferred into 100 ml fresh medium containing (per litre) 1.0 g NH 4 NO 3 , 0.5 g KH 2 PO 4 and 2.8 mg FeSO 4 . 7H 2 O, with the PAH mixture as the only carbon and energy source. PAH stock solution in chloroform was added to flasks to the same concentrations as above, and the flasks were then shaken at 160 r.p.m. for 2 days to evaporate the chloroform before inoculation. After 3 weeks incubation at 28 u C with shaking at 160 r.p.m., 1 ml culture broth was transferred repeatedly to the same medium for further enrichment. Sequential transfers were performed every 4 weeks three times. Bacteria were isolated by using the plate screening method on 216L medium (per litre seawater: 1.0 g CH 3 COONa, 10.0 g tryptone, 2.0 g yeast extract, 0.5 g sodium c...