Anderson Eric S, Paulley James T, Roop R Martin
Department of Microbiology and Immunology, East Carolina University School of Medicine, 600 Moye Boulevard, Greenville, NC 27834, USA.
J Bacteriol. 2008 Mar;190(5):1838-42. doi: 10.1128/JB.01551-07. Epub 2007 Dec 21.
Phenotypic evaluation of isogenic mutants derived from Brucella abortus 2308 indicates that the AlcR homolog DhbR (2,3-dihydroxybenzoic acid [2,3-DHBA] biosynthesis regulator) modulates the expression of the genes involved in 2,3-DHBA production, employing 2,3-DHBA or brucebactin as a coinducer.
源自流产布鲁氏菌2308的同基因突变体的表型评估表明,AlcR同源物DhbR(2,3-二羟基苯甲酸[2,3-DHBA]生物合成调节因子)利用2,3-DHBA或brucebactin作为共诱导剂来调节参与2,3-DHBA产生的基因的表达。