The maltose regulon consists of 10 genes encoding an ABC transporter for ma
ltose and maltodextrins as well as enzymes necessary for their degradation.
MalK, the energy-transducing subunit of the transport system, acts phenoty
pically as a repressor of MalT, the transcriptional activator of the mal ge
nes. Using MacConkey maltose indicator plates we isolated an insertion muta
tion that strongly reduced the repressing effect of overproduced MalK. The
insertion had occurred in treR encoding the repressor of the trehalose syst
em. The loss of TreR function led to derepression of treB encoding an enzym
eII(Tre) of the PTS for trehalose and of treC encoding TreC, the cytoplasmi
c trehalose-6-phosphate hydrolase. Further analysis revealed that maltose c
an enter the cell by facilitated diffusion through enzymeII(Tre), thus caus
ing induction of the maltose system. In addition, derepression of TreC by i
tself caused induction of the maltose system, and a mutant lacking TreC was
reduced in the uninduced level of mal gene expression indicating synthesis
of endogenous inducer by TreC. Extracts containing TreC transformed [C-14]
-maltose into another C-14-labelled compound (preliminarily identified as m
altose 1-phosphate) that is likely to be an alternative inducer of the malt
ose system.