“…Extraction and purification of total genomic DNA from the cells and PCR amplification of 16S rRNA genes were performed according to previously described methods (Jean et al, 2006b). Sequencing of the 16S rRNA genes, alignment and comparison of the resulting sequences with reference sequences available in GenBank, calculation of distance matrices for the aligned sequences and reconstruction of phylogenetic trees based on the neighbour-joining, maximum-parsimony and maximum-likelihood methods were performed as described by Shieh et al (2004) and Jean et al (2006b Kurahashi & Yokota, 2004), eight Alteromonas species (84.9-87.1 %; Bowman & McMeekin, 2005;Chiu et al, 2007;Ivanova et al, 2005;Martínez-Checa et al, 2005;Van Trappen et al, 2004a;Yoon et al, 2003Yoon et al, , 2004, two Aestuariibacter species (86.0-87.0 %; Yi et al, 2004), Bowmanella denitrificans (86.1-86.7 %; Jean et al, 2006c), eight Glaciecola species (85.0-87.9 %; Baik et al, 2006;Bowman et al, 1998;Matsuyama et al, 2006;Romanenko et al, 2003;Yong et al, 2007;Van Trappen et al, 2004b;Zhang et al, 2006) and Salinimonas chungwhensis (85.9-86.1 %; Jeon et al, 2005). The distant relationship between the two novel isolates and these bacteria was also evident in the neighbour-joining tree, in which the two isolates formed a stable monophyletic clade (bootstrap value, 100 %) located next to a sister clade comprising only Agarivorans albus strains (Fig.…”