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TonB-Dependent Heme/Hemoglobin Utilization by Caulobacter crescentus HutA
Author(s) -
Heloise Balhesteros,
Yan Shipelskiy,
Noah J. Long,
Aritri Majumdar,
Benjamin B. Katz,
Naara M. dos Santos,
Laura Leaden,
Salete M. Newton,
Marilis V. Marques,
Phillip E. Klebba
Publication year - 2016
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.00723-16
Subject(s) - ferrichrome , caulobacter crescentus , enterobactin , siderophore , escherichia coli , biology , periplasmic space , biochemistry , hemin , heme , ferric , aerobactin , hemoglobin , mutant , bacterial outer membrane , microbiology and biotechnology , enterobacteriaceae , chemistry , gene , enzyme , organic chemistry , bacterial protein
Siderophore nutrition tests withCaulobacter crescentus strain NA1000 revealed that it utilized a variety of ferric hydroxamate siderophores, including asperchromes, ferrichromes, ferrichrome A, malonichrome, and ferric aerobactin, as well as hemin and hemoglobin.C. crescentus did not transport ferrioxamine B or ferric catecholates. Because it did not use ferric enterobactin, the catecholate aposiderophore was an effective agent for iron deprivation. We determined the kinetics and thermodynamics of [59 Fe]apoferrichrome and59 Fe-citrate binding and transport by NA1000. Its affinity and uptake rate for ferrichrome (equilibrium dissociation constant [Kd ], 1 nM; Michaelis-Menten constant [KM ], 0.1 nM;V max , 19 pMol/109 cells/min) were similar to those ofEscherichia coli FhuA. Transport properties for59 Fe-citrate were similar to those ofE. coli FecA (KM , 5.3 nM;V max , 29 pMol/109 cells/min). Bioinformatic analyses implicated Fur-regulated loci00028 ,00138 ,02277 , and03023 as TonB-dependent transporters (TBDT) that participate in iron acquisition. We resolved TBDT with elevated expression under high- or low-iron conditions by SDS-PAGE of sodium sarcosinate cell envelope extracts, excised bands of interest, and analyzed them by mass spectrometry. These data identified five TBDT: three were overexpressed during iron deficiency (00028, 02277, and 03023), and 2 were overexpressed during iron repletion (00210 and 01196). CLUSTALW analyses revealed homology of putative TBDT 02277 toEscherichia coli FepA and BtuB. A Δ02277 mutant did not transport hemin or hemoglobin in nutrition tests, leading us to designate the02277 structural gene ashutA (forh eme/hemoglobinu tilization).IMPORTANCE The physiological roles of the 62 putative TBDT ofC. crescentus are mostly unknown, as are their evolutionary relationships to TBDT of other bacteria. We biochemically studied the iron uptake systems ofC. crescentus , identified potential iron transporters, and clarified the phylogenetic relationships among its numerous TBDT. Our findings identified the first outer membrane protein involved in iron acquisition byC. crescentus , its heme/hemoglobin transporter (HutA).

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