A novel actinomycete, designated strain S1.4 T , was isolated from a soil sample collected from Kenilworth Racecourse in the Western Cape, South Africa. The strain was able to grow in the presence of 5 % NaCl. It contained LL-diaminopimelic acid and glycine in the cell-wall peptidoglycan with glucose present in the whole-cell sugar profile. Strain S1.4 T was shown to be a member of either the genus Kribbella or the genus Nocardioides based on a rapid molecular identification method by using single-enzyme restriction endonuclease digestion of the PCR-amplified 16S rRNA gene with MboI, VspI, SphI, SnaBI, SalI and AgeI. Analysis of the 16S rRNA gene sequence indicated that strain S1.4 T belonged to the genus Kribbella. Phylogenetic analysis based on 16S rRNA gene sequence comparisons showed that strain S1.4 T was related most closely to Kribbella solani DSA1 T . Strain S1.4 T was phenotypically distinct from K. solani DSA1 T and was shown to be a separate genomic species based on DNA-DNA hybridization experiments (40.4±3.8 % DNA-DNA relatedness between the two). Strain S1.4 T (5DSM 19227 T 5NRRL B-24553 T ) is thus presented as the type strain of a novel species, for which the name Kribbella hippodromi sp. nov. is proposed.The genus Kribbella was proposed by Park et al. (1999) and contains nocardioform actinomycetes with LL-diaminopimelic acid in the cell wall. With the transfer of Hongia koreensis to the genus (Sohn et al., 2003) and more recently the descriptions of Kribbella karoonensis and Kribbella swartbergensis (Kirby et al., 2006) and Kribbella aluminosa (Carlsohn et al., 2007) there are, at the time of writing, 12 recognized Kribbella species (Euzéby, 2007). Here we describe the characterization of a novel member of the genus, isolated from a soil sample collected from a racecourse in the Western Cape, South Africa. Strain S1.4 T was isolated from soil collected in the fynbosrich area surrounded by the horse racing track at Kenilworth Racecourse, Cape Town, South Africa. The soil was ground in a pestle and mortar before being heated at 60 u C for 1 h, after which 0.1 g was added to 1 ml of sterile distilled water and agitated by vortexing for 1 min. The sample was serially diluted in sterile distilled water and spread-plated on SM1 agar (Tan et al., 2006) containing cycloheximide (50 mg ml 21 ) and nalidixic acid (10 mg ml 21 ). Strain S1.4 T was isolated after incubation at 30 u C for 21 days and was subsequently maintained on yeast extract-malt extract agar (ISP 2 medium) (Shirling & Gottlieb, 1966).Genomic DNA was extracted as described by Wang et al. (1996), with modifications to the lysis buffer to increase the lysozyme concentration to 20 mg ml 21 and to include proteinase K (0.2 mg ml 21 ); digestion was performed overnight. Treatment with RNase A was performed overnight. To allow rapid identification of the isolate to the genus level, 16S rRNA gene sequence amplification and restriction endonuclease digestion were performed as described by Cook & Meyers (2003), by using single digestions with the ...