An actinomycete, designated FXJ1.102 T , was isolated from acidic soil collected in Jiangxi Province, south-east China. Phylogenetic analysis based on 16S rRNA gene sequences indicated that strain FXJ1.102 T belonged to the genus Nonomuraea and was most closely related to Nonomuraea candida HMC10 T , Nonomuraea turkmeniaca DSM 43926 T , Nonomuraea antimicrobica YIM 61105 T and 'Nonomuraea aegyptia' S136 (98.9, 98.3, 97.9 and 97.5 % 16S rRNA gene sequence similarities, respectively). The morphological characteristics were typical of the genus Nonomuraea. The chemotaxonomic properties, such as cell-wall chemotype IIIB, phospholipid type IV, MK-9(H 4 ) as the major menaquinone and iso-C 16 : 0 (22.2 %) as the major fatty acid, supported the assignment of the strain to the genus Nonomuraea. DNA-DNA relatedness and physiological tests allowed genotypic and phenotypic differentiation of strain FXJ1.102 T from its closest phylogenetic relatives. The isolate therefore represents a novel species, for which the name Nonomuraea jiangxiensis sp. nov. is proposed. The type strain is FXJ1.102 T (5CGMCC 4.6533 T 5NBRC 106679 T ).The genus Nonomuraea, the spelling of which was corrected by Chiba et al. (1999), was originally proposed by Zhang et al. (1998) as a member of the family Streptosporangiaceae, which forms extensively branched substrate and aerial mycelia. The type species is Nonomuraea pusilla. At the time of writing, the genus Nonomuraea comprised 27 species and two subspecies with validly published names (http:// www.bacterio.cict.fr/index.html), which were established on the basis of a polyphasic approach (Gyobu & Miyadoh, 2001;Stackebrandt et al., 2001;Quintana et al., 2003; Ara et al., 2007a, b;Le Roes & Meyers, 2008; Kämpfer et al., 2010;Wang et al., 2011;Zhao et al., 2011;Xi et al., 2011). Strain FXJ1.102 T was isolated from acidic soil (pH 5.0) collected from Jiangxi Agricultural University, Nanchang city, Jiangxi Province, China. The sample was dried at room temperature, ground into powder and then suspended in sterile distilled water and serially diluted. The diluted soil suspension was incubated on humic acid-vitamin agar (pH 5.0;Hayakawa & Nonomura, 1987) supplemented with (mg l 21 ) cycloheximide (50), nystatin (50) and nalidixic acid (20) at 28 u C for 3 weeks. The strain was maintained on glucose-yeast extract-malt extract agar [International Streptomyces Project medium 2 (ISP 2), pH 5.0; Shirling & Gottlieb, 1966] at 4 u C and as suspensions of mycelial fragments in 20 % (v/v) glycerol at 220 u C.The morphological properties of the isolate were examined by light microscopy (Zeiss Axioskop) and scanning electron microscopy (model FEI Quanta 200) using cultures grown on ISP 2 at 28 u C for 14 days. For cultural characterization, the isolate was grown at 28 u C for 14-21 days on various agar media as described by Waksman (1961) and Shirling & Gottlieb (1966). Growth at pH 4.0-11.0 (at intervals of one pH unit) was determined on Bennett's medium at 28 u C for 14 days. Growth at 4, 10, 15, 20, 28, 37, 45 ...