I. Sanogueira et al., THE BACILLUS-SUBTILIS L-ARABINOSE (ARA) OPERON - NUCLEOTIDE-SEQUENCE,GENETIC ORGANIZATION AND EXPRESSION, Microbiology, 143, 1997, pp. 957-969
The Bacillus subtilis L-arabinose metabolic genes araA, araB and araD,
encoding L-arabinose isomerase, L-ribulokinase and L-ribulose-5-phosp
hate 4-epimerase, respectively, have been cloned previously and the pr
oducts of araB and araD were shown to be functionally homologous to th
eir Escherichia coil counterparts by complementation experiments, Here
we report that araA, araB and araD, whose inactivation leads to an Ar
a(-) phenotype, are the first three ORFs of a nine cistron transcripti
onal unit with a total length of 11 kb, This operon, called ara, is lo
cated at about 256 degrees on the B, subtilis genetic map and contains
six new genes named araL, araM, araN, araP, araQ and abfA, Expression
of the ara operon is directed by a strong sigma(A)-like promoter iden
tified within a 150 bp DNA fragment upstream from the translation star
t site of araA, Analysis of the sequence of the ara operon showed that
the putative products of araN, araP and araQ are homologous to bacter
ial components of binding-protein-dependent transport systems and abfA
most probably encodes an alpha-L-arabinofuranosidase. The functions o
f araL and araM are unknown, An in vitro constructed insertion-deletio
n mutation in the region downstream from araD allowed us to demonstrat
e that araL, araM, araN, araP, araq and abfA are not essential for L-a
rabinose utilization. Studies with strains bearing transcriptional fus
ions of the operon to the E. coil lacZ gene revealed that expression f
rom the ara promoter is induced by L-arabinose and repressed by glucos
e.