Deinobacterium chartae gen. nov., sp. nov., an extremely radiation-resistant, biofilm-forming bacterium isolated from a Finnish paper mill A rod-shaped, non-spore-forming, non-motile, aerobic, oxidase and catalase-positive and radiation-resistant bacterium (designated strain K4.1 T ) was isolated from biofilm collected from a Finnish paper mill. The bacterium grew as pale pink colonies on oligotrophic medium at 12 to 50 6C (optimum 37 to 45 6C) and at pH 6 to 10.3. The DNA G+C content of the strain was 66.8 mol%. According to 16S rRNA gene sequence analysis, strain K4.1 T was distantly related to the genus Deinococcus, sharing highest similarity with Deinococcus pimensis (90.0 %). In the phylogenetic tree, strain K4.1 T formed a separate branch in the vicinity of the genus Deinococcus.The peptidoglycan type was A3b with L-Orn-Gly-Gly and the quinone system was determined to be MK-8. The polar lipid profile of strain K4.1 T differed markedly from that of the genusDeinococcus. The predominant lipid of strain K4.1 T was an unknown aminophospholipid and it did not contain the unknown phosphoglycolipid predominant in the polar lipid profiles of deinococci analysed to date. Two of the predominant fatty acids of the strain, 15 : 0 anteiso and 17 : 0 anteiso, were lacking or present in small amounts in species of the genus Deinococcus. Phylogenetic distinctness and significant differences in the polar lipid and fatty acid profiles suggest classification of strain K4.1 T as a novel genus and species in the family Deinococcaceae, for which we propose the name Deinobacterium chartae gen. nov., sp. nov. Ferreira et al., 1997). Truepera radiovictrix was also isolated from a geothermal spring (Albuquerque et al., 2005). Deinococcus geothermalis is known as a common colonizer in paper machines (Kolari et al., 2003;Peltola et al., 2008).Strain K4.1 T was isolated from a biofilm growing in the wire section of a Finnish paper mill (wire water temperature 45-50 u C) producing folding boxboard. Biofilm was collected with a sterile plastic tube and transported to the laboratory on the same day. The biofilm was washed with sterile tap water to remove loosely attached bacteria. Washed pieces of the biofilm were incubated on a polystyrene 12-well plate in sterilized board mill wire water amended with 1.0 g soluble starch and 0.1 g yeast extract per litre. After 2 days of shaking at 160 r.p.m., 48 u C, freshly grown biofilm from the edges of the well was streaked on a plate of paper machine water (PMW) agar (wire water from the machine in question supplemented with 1.0 g soluble starch, 0.1 g yeast extract and 15 g agar per litre) and grown for 4 days at 48 u C. A pale pink colony (strain K4.1 T ) was isolated from this plate and subcultured until pure on PMW agar plates.Abbreviations: PMW, paper machine water; SEM, scanning electron microscopy; TEM, transmission electron microscopy.