Kubota Takeshi, Tanaka Yuya, Takemoto Norihiko, Watanabe Akira, Hiraga Kazumi, Inui Masayuki, Yukawa Hideaki
Research Institute of Innovative Technology for the Earth (RITE), 9-2, Kizugawadai, Kizugawa, Kyoto, 619-0292, Japan.
Mol Microbiol. 2014 Apr;92(2):356-68. doi: 10.1111/mmi.12560. Epub 2014 Mar 10.
The qsu operon of Corynebacterium glutamicum comprises four genes (qsuABCD) that underpin the microorganism's quinate/shikimate utilization pathways. The genes encode enzymes that catalyse reactions at the metabolic branch point between the biosynthesis route for synthesis of aromatic compounds and the catabolic route for degradation of quinate and shikimate for energy production. A qsuR gene located immediately upstream of qsuA encodes a protein (QsuR) which activates the operon in the presence of quinate or shikimate. Three observations support chorismate, an intermediate of the biosynthesis route, as a direct effector of QsuR: First, induction of qsuA mRNA in the presence of either quinate or shikimate disappears upon deletion of the gene encoding chorismate synthase. Second, chorismate accumulates when the operon is induced. Third, a DNase I-protected segment by QsuR is shortened in the presence of chorismate. The QsuR tetramer senses the accumulation of chorismate and activates qsu genes that promote the quinate/shikimate catabolic instead of the aromatic compounds biosynthetic route. Such chorismate-dependent control of carbon flow has not been previously described.
谷氨酸棒杆菌的qsu操纵子由四个基因(qsuABCD)组成,这些基因支撑着微生物的奎尼酸/莽草酸利用途径。这些基因编码的酶催化芳香族化合物生物合成途径与奎尼酸和莽草酸分解代谢途径之间代谢分支点的反应,后者用于产生能量。位于qsuA上游紧邻的qsuR基因编码一种蛋白质(QsuR),该蛋白质在奎尼酸或莽草酸存在时激活操纵子。有三个观察结果支持分支酸(生物合成途径的一种中间产物)作为QsuR的直接效应物:第一,在编码分支酸合酶的基因缺失后,在奎尼酸或莽草酸存在下qsuA mRNA的诱导消失。第二,操纵子被诱导时分支酸会积累。第三,在分支酸存在时,QsuR保护的一段DNA酶I敏感片段会缩短。QsuR四聚体感知分支酸的积累,并激活促进奎尼酸/莽草酸分解代谢而非芳香族化合物生物合成途径的qsu基因。这种依赖分支酸的碳流控制此前尚未见报道。