Nas Megan Y, Gabell Jeffrey, Inniss Nicole, Minasov George, Shuvalova Ludmilla, Satchell Karla J F, Cianciotto Nicholas P
Department of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Acta Crystallogr F Struct Biol Commun. 2025 Jul 1;81(Pt 7):287-296. doi: 10.1107/S2053230X2500490X. Epub 2025 Jun 4.
Clinical and environmental isolates of Stenotrophomonas maltophilia produce an enterobactin-like siderophore that promotes bacterial growth under low-iron conditions. Although prior mutational and bioinformatic analyses indicated that most of the enzymes encoded by the S. maltophilia entCEBB'FA locus are suitably reminiscent of their counterparts in Escherichia coli and other bacteria, Stenotrophomonas EntB was unusual. In bacteria producing enterobactin-related molecules, EntB and its homologs are usually multi-domain proteins in which the amino portion acts as an isochorismatase and the carboxy domain serves as an aryl carrier protein (ArCP). However, in S. maltophilia the isochorismatase and ArCP functions are encoded by two distinct genes: entB and entB', respectively. Current mutant analysis was used to first confirm that S. maltophilia entB is needed for siderophore activity and bacterial growth in iron-depleted media. A crystal structure of S. maltophilia EntB was then obtained. The structure aligned with the N-terminal portion of EntB from E. coli and VibB from Vibrio cholerae, affirming the protein to be a single-domain isochorismatase. However, S. maltophilia EntB also aligned with the single-domain PhzD from Pseudomonas aeruginosa, which is a key enzyme involved in the biosynthesis of the antimicrobial compound phenazine. BLASTP searches indicated that entB and its neighboring genes are fully conserved amongst S. maltophilia strains but are variably present in other Stenotrophomonas species. The closest homologs to S. maltophilia EntB outside the genus were hypothetical proteins/putative isochorismatases in some Gram-negative bacteria (for example Pseudomonas spp. and Xanthomonas spp.), Gram-positive bacteria (Streptomyces spp. and Bacillus subtilis) and fungi (for example Rhizopus arrhizus and Knufia peltigerae).
嗜麦芽窄食单胞菌的临床分离株和环境分离株可产生一种类肠杆菌素的铁载体,该铁载体可在低铁条件下促进细菌生长。尽管先前的突变分析和生物信息学分析表明,嗜麦芽窄食单胞菌entCEBB'FA基因座编码的大多数酶与大肠杆菌和其他细菌中的对应酶相似,但嗜麦芽窄食单胞菌的EntB却不同寻常。在产生与肠杆菌素相关分子的细菌中,EntB及其同源物通常是多结构域蛋白,其中氨基部分充当异分支酸酶,羧基结构域充当芳基载体蛋白(ArCP)。然而,在嗜麦芽窄食单胞菌中,异分支酸酶和ArCP功能分别由两个不同的基因编码:entB和entB'。目前的突变分析首先用于确认嗜麦芽窄食单胞菌entB对于铁载体活性以及缺铁培养基中细菌的生长是必需的。随后获得了嗜麦芽窄食单胞菌EntB的晶体结构。该结构与大肠杆菌的EntB的N端部分以及霍乱弧菌的VibB对齐,证实该蛋白是单结构域异分支酸酶。然而,嗜麦芽窄食单胞菌EntB也与铜绿假单胞菌的单结构域PhzD对齐,PhzD是参与抗菌化合物吩嗪生物合成的关键酶。BLASTP搜索表明,entB及其相邻基因在嗜麦芽窄食单胞菌菌株中完全保守,但在其他嗜麦芽窄食单胞菌物种中存在差异。在该属之外,与嗜麦芽窄食单胞菌EntB最接近的同源物是一些革兰氏阴性细菌(例如假单胞菌属和黄单胞菌属)、革兰氏阳性细菌(链霉菌属和枯草芽孢杆菌)和真菌(例如少根根霉和皮氏克努夫酵母)中的假想蛋白/推定异分支酸酶。