C. Seeger et al., IDENTIFICATION AND CHARACTERIZATION OF GENES (XAPA, XAPB, AND XAPR) INVOLVED IN XANTHOSINE CATABOLISM IN ESCHERICHIA-COLI, Journal of bacteriology, 177(19), 1995, pp. 5506-5516
We have characterized four genes from the 52-min region on the Escheri
chia coli linkage map. Three of these genes are directly involved in t
he metabolism of xanthosine, whereas the function of the fourth gene i
s unknown. One of the genes (xapA) encodes xanthosine phosphorylase. T
he second gene, named xapB, encodes a polypeptide that shows strong si
milarity to the nucleoside transport protein NupG, The genes xapA and
xapB are located clockwise of a gene identified as xapR, which encodes
a positive regulator belonging to the LysR family and is required for
the expression of xapA and xapB. The genes xapA and xapB form an oper
on, and their expression was strictly dependent on the presence of bot
h the XapR protein and the inducer xanthosine. Expression of tile xapR
gene is constitutive and not autoregulated, unlike the case for many
other LysR family proteins. In minicells, the XapB polypeptide was fou
nd primarily in the membrane fraction, indicating that XapB is a trans
port protein like NupG and is involved in the transport of xanthosine.