TY - JOUR
T1 - Probing direct interactions between CodY and the oppD promoter of Lactococcus lactis
AU - Den Hengst, Chris D.
AU - Curley, Peter
AU - Larsen, Rasmus
AU - Buist, Girbe
AU - Nauta, Arjen
AU - Van Sinderen, Douwe
AU - Kuipers, Oscar P.
AU - Kok, Jan
PY - 2005/1
Y1 - 2005/1
N2 - CodY of Lactococcus lactis MG1363 is a transcriptional regulator that represses the expression of several genes encoding proteins of the proteolytic system. These genes include pepN, pepC, opp-pepO1, and probably prtPM, pepX, and pepDA2, since the expression of the latter three genes relative to nitrogen availability is similar to that of the former. By means of in vitro DNA binding assays and DNase I footprinting techniques, we demonstrate that L. lactis CodY interacts directly with a region upstream of the promoter of its major target known so far, the opp system. Our results indicate that multiple molecules of CodY interact with this promoter and that the amount of bound CodY molecules is affected by the presence of branched-chain amino acids and not by GTP. Addition of these amino acids strongly affects the extent of the region protected by CodY in DNase I footprints. Random and site-directed metagenesis of the upstream region of oppD yielded variants that were derepressed in a medium with an excess of nitrogen sources. Binding studies revealed the importance of specific bases in the promoter region required for recognition by CodY.
AB - CodY of Lactococcus lactis MG1363 is a transcriptional regulator that represses the expression of several genes encoding proteins of the proteolytic system. These genes include pepN, pepC, opp-pepO1, and probably prtPM, pepX, and pepDA2, since the expression of the latter three genes relative to nitrogen availability is similar to that of the former. By means of in vitro DNA binding assays and DNase I footprinting techniques, we demonstrate that L. lactis CodY interacts directly with a region upstream of the promoter of its major target known so far, the opp system. Our results indicate that multiple molecules of CodY interact with this promoter and that the amount of bound CodY molecules is affected by the presence of branched-chain amino acids and not by GTP. Addition of these amino acids strongly affects the extent of the region protected by CodY in DNase I footprints. Random and site-directed metagenesis of the upstream region of oppD yielded variants that were derepressed in a medium with an excess of nitrogen sources. Binding studies revealed the importance of specific bases in the promoter region required for recognition by CodY.
UR - https://www.scopus.com/pages/publications/11844277701
U2 - 10.1128/JB.187.2.512-521.2005
DO - 10.1128/JB.187.2.512-521.2005
M3 - Article
C2 - 15629923
AN - SCOPUS:11844277701
SN - 0021-9193
VL - 187
SP - 512
EP - 521
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 2
ER -