Kim Ok Bin, Unden Gottfried
Institut für Mikrobiologie und Weinforschung, Johannes Gutenberg-Universität Mainz, Becherweg 15, 55099 Mainz, Germany.
J Bacteriol. 2007 Mar;189(5):1597-603. doi: 10.1128/JB.01402-06. Epub 2006 Dec 15.
Escherichia coli ferments L-tartrate under anaerobic conditions in the presence of an additional electron donor to succinate. The carrier for L-tartrate uptake and succinate export and its relation to the general C(4)-dicarboxylate carriers DcuA, DcuB, and DcuC were studied. The secondary carrier TtdT, encoded by the ttdT (previously called ygjE) gene, is required for the uptake of L-tartrate. The ttdT gene is located downstream of the ttdA and ttdB genes, encoding the L-tartrate dehydratase TtdAB. Analysis of mRNA by reverse transcription-PCR showed that ttdA, ttdB, and ttdT are cotranscribed. Deletion of ttdT abolished growth by L-tartrate and degradation of L-tartrate completely. Bacteria containing TtdT catalyze L-tartrate or succinate uptake and specific heterologous L-tartrate/succinate antiporting. D-Tartrate is not a substrate for TtdT. TtdT operates preferentially in the direction of tartrate uptake and succinate excretion. The Dcu carriers do not support anaerobic growth on L-tartrate or L-tartrate transport. TtdT is related in sequence and function to CitT, which catalyzes heterologous citrate/succinate antiporting in citrate fermentation.
在厌氧条件下,大肠杆菌在存在额外电子供体生成琥珀酸的情况下发酵L-酒石酸盐。研究了L-酒石酸盐摄取和琥珀酸输出的载体及其与通用C(4)-二羧酸载体DcuA、DcuB和DcuC的关系。由ttdT(以前称为ygjE)基因编码的二级载体TtdT是L-酒石酸盐摄取所必需的。ttdT基因位于编码L-酒石酸脱水酶TtdAB的ttdA和ttdB基因的下游。通过逆转录PCR对mRNA的分析表明,ttdA、ttdB和ttdT是共转录的。ttdT的缺失完全消除了L-酒石酸盐的生长和L-酒石酸盐的降解。含有TtdT的细菌催化L-酒石酸盐或琥珀酸的摄取以及特定的异源L-酒石酸盐/琥珀酸反向转运。D-酒石酸盐不是TtdT的底物。TtdT优先在酒石酸盐摄取和琥珀酸排泄的方向上起作用。Dcu载体不支持在L-酒石酸盐上的厌氧生长或L-酒石酸盐的运输。TtdT在序列和功能上与CitT相关,CitT在柠檬酸盐发酵中催化异源柠檬酸盐/琥珀酸反向转运。