A slightly curved, rod-shaped marine bacterium, designated strain CL-S1 T , was isolated from near Dokdo, an island in the East Sea, Korea. Cells were Gram-negative and grew well under either aerobic or microaerobic conditions. Analyses of the 16S rRNA and gyrA gene sequences of strain CL-S1 T revealed an affiliation with the genus Arcobacter within the class Epsilonproteobacteria. Phylogenetic analyses based on 16S rRNA and gyrA gene sequences showed that strain CL-S1 T formed a robust clade with Arcobacter halophilus LA31B T , with sequence similarities of 96.1 and 88.2 %, respectively. DNA-DNA relatedness between strain CL-S1 T and A. halophilus DSM 18005 T was 44 %, indicating that they represent genomically distinct species. Strain CL-S1 T grew optimally at 30-37 6C, at pH 7 and in the presence of 3-5 % NaCl. The dominant cellular fatty acids were iso-C 15 : 0 2-OH and/or C 16 : 1 v7c (28.4 %), C 16 : 0 (26.2 %) and C 18 : 1 v7c (22.3 %). The DNA G+C content of strain CL-S1 T was 28 mol%. Strain CL-S1 T differed phenotypically from A. halophilus LA31B T based on its ability to grow aerobically at 10 6C and inability to grow under anaerobic conditions. Based on the data presented, strain CL-S1 T is considered to represent a novel species of the genus Arcobacter, for which the name Arcobacter marinus sp. nov. is proposed. The type strain is CL-S1 T (5KCCM 90072 T 5JCM 15502 T ).The genus Arcobacter belongs to the family Campylobacteraceae, which also contains the genera Campylobacter and Sulfurospirillum ( (Neill et al., 1985;Kiehlbauch et al., 1991;Vandamme et al., 1992) and are recognized as potential emerging human pathogens (Mansfield & Forsythe, 2000). A. nitrofigilis was isolated from Spartina alterniflora roots in a salt marsh (McClung et al., 1983). A. halophilus and A. cibarius were isolated from a hypersaline lagoon (Donachie et al., 2005) and the skin of a broiler carcass (Houf et al., 2005), respectively. In the present study, a novel strain affiliated with the genus Arcobacter was isolated and subjected to a polyphasic taxonomic analysis.Seaweeds and a starfish were collected and added to a surface seawater sample (50 ml) taken from the vicinity of Dokdo, an island in the East Sea, Korea. The mixture was maintained at 4 u C for 15 days. The mixture was then homogenized by using a blender and an aliquot (50 ml) was spread onto MY medium (Bouchotroch et al., 2001). The culture was incubated aerobically at 30 u C for 2 weeks. Strain CL-S1 T was isolated and subsequently purified on fresh marine agar 2216 (MA; Difco). Strain CL-S1 T grew well on MA or on saline blood agar [SBA; per litre distilled water: 40 g blood agar base (BBL), 50 ml sheep blood, 30 g NaCl] at 37 u C under either aerobic or microaerobic conditions. The novel strain was preserved in marine broth 2216 (MB; Difco) supplemented with 30 % (v/v) glycerol at 280 u C.For 16S rRNA gene amplification by PCR, DNA was extracted from a single colony by a boiling method (Englen & Kelley, 2000). The crude extracts served as the DNA template for...