Abstract
Thirty Gluconobacter strains maintained at Culture Collection NBRC were re-identified at the species level on the basis of restriction analysis of 16S-23S rDNA internal transcribed spacer (ITS) regions by digestion with two restriction endonucleases Mboll and Bsp1286l. The strains examined were divided into seven groups, designated as Group I and Group III-VIII, by the combination of the restriction patterns obtained with the two restriction endonucleases. Group I included seven strains, which gave G. oxydans patterns with the two restriction endonucleases and were re-identified as G. oxydans. Group III included 12 strains, which gave G. frateurii patterns and were re-identified as G. frateurii. Group IV included six strains, which gave G. cerinus pattern with Mboll and G. frateurii pattern with Bsp12861 and were re-identified as G. frateurii. Group V included one strain (NBRC 3274), which gave respectively G. frateurii pattern and G. cerinus, pattern and was re-identified as G. cerinus. Group VI included one strain (NBRC 3990), which gave respectively G. oxydans pattern and an unidentified restriction pattern and was re-identified temporarily as G. oxydans. Group VII included two strains (NBRC 3250 and NBRC 3273), which gave respectively an unidentified restriction pattern and G. oxydans pattern. Group VIII included one strain (NBRC 3266), which gave unidentified restriction patterns. The three strains of Group VII and Group VIII were suggested to constitute new taxa by sequencing of 16S-23S rDNA ITS regions.
