A yellow-pigmented, hexachlorocyclohexane (HCH)-degrading bacterium, strain IP26 T , was isolated from an HCH dumpsite and subjected to a polyphasic analysis in order to determine its taxonomic position. Strain IP26 T showed maximum 16S rRNA gene sequence similarity with Sphingobium francense Sp+ T (98.5 %), Sphingobium japonicum UT26 T (98.4 %) and Sphingobium indicum B90A T (98.2 %). Phylogenetic analysis based on 16S rRNA gene sequences also showed that strain IP26 T formed a cluster with these three HCH-degrading strains. Chemotaxonomic data (major polyamine, spermidine; major quinone, ubiquinone with ten isoprene units; major polar lipids, phosphatidylmonomethylethanolamine, phosphatidylethanolamine, diphosphatidylglycerol, phosphotidylcholine; and presence of 2-hydroxy fatty acid) supported inclusion of strain IP26 T in the genus Sphingobium. However, the results of DNA-DNA hybridization and morphological and biochemical tests clearly allowed phenotypic and genotypic differentiation of strain IP26 T from recognized species of the genus Sphingobium. Strain IP26 T thus represents a novel species of the genus Sphingobium for which the name Sphingobium chinhatense sp. nov. is proposed. The type strain is IP26 T (5MTCC8598 T 5CCM 7432 T ).Hexachlorocyclohexane (HCH) contamination can occur as a result of the unusual production process of this compound . HCH is prepared by the chlorination of benzene in the presence of UV. This generally leads to the production of four main HCH isomers, a-, b-, c-and d-, in the ratio 60-70, 5-12, 10-12 and 6-10 %, respectively (Willett et al., 1998). Among these, only c-HCH, also called lindane, has insecticidal activity. During the purification process, the remaining isomers (one tonne of lindane produces nine tonnes of HCH waste) are discarded in the open, thus creating an HCH-contaminated dumpsite. We discovered one such dumpsite in the vicinity of an industry that has been producing lindane for the past 10 years (Dadhwal et al., 2009). Around 24 bacterial strains were isolated from these sites and their potential to degrade HCH isomers was evaluated (Dadhwal et al., 2009). Some of these bacterial isolates have been characterized by using a polyphasic approach (Kumar et al., 2008;Singh & Lal, 2009).Strain IP26 T was isolated from highly HCH-contaminated soil by culturing on LB agar using a serial dilution method (Dadhwal et al., 2009). The strain was found to degrade a-, b-, c-and d-HCH isomers faster than Sphingobium indicum B90A T (Dadhwal et al., 2009) (Supplementary Fig. S1, available in IJSEM Online). Strain IP26 T was characterized taxonomically and found to represent a novel species of Sphingobium.Colony size, shape and colour were studied on LB agar plates incubated at 28 uC. Gram-staining and sporestaining were performed using HiMedia kits. Motility of strain IP26 T was assessed by the hanging drop method as well as on motility agar medium. Catalase and oxidase tests were carried out as described by McCarthy & Cross (1984). Hydrolysis of aesculin and Tween 80 and ...