Gluconobacter oxydans ATCC 9937 was subjected to transposon mutagenesis usi
ng Tn5. A non-pigmented mutant was shown to be defective in gluconic acid d
ehydrogenase and to produce gluconic acid from glucose, whereas the parent
strain produced 2,5-diketogluconic acid. Cloning and sequencing of the regi
on containing the Tn5 insertion showed that the insertion point occurred in
an open reading frame homologous (42% amino acid identity) to the ribF gen
es of Pseudomonas fluorescens and Escherichia coli. The resulting lack of a
riboflavin cofactor would explain the loss of enzyme activity. (C) 1999 Pu
blished by Elsevier Science B.V. All rights reserved.