Previous Article | Next Article 
J Bacteriol. 1993 June; 175(11): 3317-3326
Analysis of mutants of Salmonella typhimurium defective in the synthesis of the nucleotide loop of cobalamin.
G A O'Toole,
M R Rondon and
J C Escalante-Semerena
Department of Bacteriology, University of Wisconsin, Madison 53706.
ABSTRACT
The CobIII region of the cobalamin (CBL) biosynthetic (cob) operon of Salmonella typhimurium encodes functions necessary for the synthesis of the nucleotide loop of CBL and comprises three genes, designated cobU, cobS, and cobT (26). Complementation studies identified two classes of CobIII mutants: (i) 34 mutants were complemented by a plasmid carrying the cobU+ gene, and (ii) 27 mutants were complemented by a plasmid carrying the cobS+ gene; none of the mutants tested was complemented by the cobT+ clone, a result suggesting that no cobT mutations were isolated. These data were consistent with those of complementation studies done with F' cobUST plasmids, which also suggested that the CobIII region comprises two complementation groups. A plasmid carrying cobUS+ was sufficient to complement a deletion of the entire CobIII region, a result suggesting that CobT was not required for CBL biosynthesis. Nutritional studies done with synthetic putative intermediates of the CobIII pathway were performed to further classify cobIII mutants. A subset of cobU mutants were found to be responsive to exogenous dicyano-cobinamide-GDP, while cobS mutants were found to be responsive only to CBL. These results are consistent with the adenosyl-cobinamide kinase-GTP:adenosyl-cobinamide-phosphate guanylyltransferase and CBL synthase activities proposed for CobU and CobS, respectively. The cobIII genes under the control of the T7 promoter were overexpressed, and the resulting polypeptides were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Three polypeptides with apparent molecular masses of 22, 26 and 39 kDa, consistent with the predicted masses for CobU, CobS, and CobT, respectively, were detected.
J Bacteriol. 1993 June; 175(11): 3317-3326
This article has been cited by other articles:
-
Boyd, J. M., Lewis, J. A., Escalante-Semerena, J. C., Downs, D. M.
(2008). Salmonella enterica Requires ApbC Function for Growth on Tricarballylate: Evidence of Functional Redundancy between ApbC and IscU. J. Bacteriol.
190: 4596-4602
[Abstract]
[Full Text]
-
Santos, F., Vera, J. L., van der Heijden, R., Valdez, G., de Vos, W. M., Sesma, F., Hugenholtz, J.
(2008). The complete coenzyme B12 biosynthesis gene cluster of Lactobacillus reuteri CRL1098. Microbiology
154: 81-93
[Abstract]
[Full Text]
-
Zayas, C. L., Claas, K., Escalante-Semerena, J. C.
(2007). The CbiB Protein of Salmonella enterica Is an Integral Membrane Protein Involved in the Last Step of the De Novo Corrin Ring Biosynthetic Pathway. J. Bacteriol.
189: 7697-7708
[Abstract]
[Full Text]
-
Escalante-Semerena, J. C.
(2007). Conversion of Cobinamide into Adenosylcobamide in Bacteria and Archaea. J. Bacteriol.
189: 4555-4560
[Full Text]
-
Zayas, C. L., Escalante-Semerena, J. C.
(2007). Reassessment of the Late Steps of Coenzyme B12 Synthesis in Salmonella enterica: Evidence that Dephosphorylation of Adenosylcobalamin-5'-Phosphate by the CobC Phosphatase Is the Last Step of the Pathway. J. Bacteriol.
189: 2210-2218
[Abstract]
[Full Text]
-
Zayas, C. L., Woodson, J. D., Escalante-Semerena, J. C.
(2006). The cobZ Gene of Methanosarcina mazei Go1 Encodes the Nonorthologous Replacement of the {alpha}-Ribazole-5'-Phosphate Phosphatase (CobC) Enzyme of Salmonella enterica.. J. Bacteriol.
188: 2740-2743
[Abstract]
[Full Text]
-
Woodson, J. D., Reynolds, A. A., Escalante-Semerena, J. C.
(2005). ABC Transporter for Corrinoids in Halobacterium sp. Strain NRC-1. J. Bacteriol.
187: 5901-5909
[Abstract]
[Full Text]
-
Maggio-Hall, L. A., Claas, K. R., Escalante-Semerena, J. C.
(2004). The last step in coenzyme B12 synthesis is localized to the cell membrane in bacteria and archaea. Microbiology
150: 1385-1395
[Abstract]
[Full Text]
-
Maggio-Hall, L. A., Escalante-Semerena, J. C.
(2003). {alpha}-5,6-Dimethylbenzimidazole adenine dinucleotide ({alpha}-DAD), a putative new intermediate of coenzyme B12 biosynthesis in Salmonella typhimurium. Microbiology
149: 983-990
[Abstract]
[Full Text]
-
Cheong, C.-G., Escalante-Semerena, J. C., Rayment, I.
(2002). Capture of a Labile Substrate by Expulsion of Water Molecules from the Active Site of Nicotinate Mononucleotide:5,6-Dimethylbenzimidazole Phosphoribosyltransferase (CobT) from Salmonella enterica. J. Biol. Chem.
277: 41120-41127
[Abstract]
[Full Text]
-
Maggio-Hall, L. A., Escalante-Semerena, J. C.
(1999). In vitro synthesis of the nucleotide loop of cobalamin by Salmonella typhimurium enzymes. Proc. Natl. Acad. Sci. USA
96: 11798-11803
[Abstract]
[Full Text]
-
Tsang, A. W., Horswill, A. R., Escalante-Semerena, J. C.
(1998). Studies of Regulation of Expression of the Propionate (prpBCDE) Operon Provide Insights into How Salmonella typhimurium LT2 Integrates Its 1,2-Propanediol and Propionate Catabolic Pathways. J. Bacteriol.
180: 6511-6518
[Abstract]
[Full Text]
-
Tsang, A. W., Escalante-Semerena, J. C.
(1998). CobB, a New Member of the SIR2 Family of Eucaryotic Regulatory Proteins, Is Required to Compensate for the Lack of Nicotinate Mononucleotide:5,6-Dimethylbenzimidazole Phosphoribosyltransferase Activity in cobT Mutants during Cobalamin Biosynthesis in Salmonella typhimurium LT2. J. Biol. Chem.
273: 31788-31794
[Abstract]
[Full Text]
-
Brushaber, K. R., O'Toole, G. A., Escalante-Semerena, J. C.
(1998). CobD, a Novel Enzyme with L-Threonine-O-3-phosphate Decarboxylase Activity, Is Responsible for the Synthesis of (R)-1-Amino-2-propanol O-2-Phosphate, a Proposed New Intermediate in Cobalamin Biosynthesis in Salmonella typhimurium LT2. J. Biol. Chem.
273: 2684-2691
[Abstract]
[Full Text]
-
Trzebiatowski, J. R., Escalante-Semerena, J. C.
(1997). Purification and Characterization of CobT, the Nicotinate-mononucleotide:5,6-Dimethylbenzimidazole Phosphoribosyltransferase Enzyme from Salmonella typhimurium LT2. J. Biol. Chem.
272: 17662-17667
[Abstract]
[Full Text]
-
O'Toole, G. A., Escalante-Semerena, J. C.
(1995). Purification and Characterization of the Bifunctional CobU Enzyme of Salmonella typhimurium LT2. J. Biol. Chem.
270: 23560-23569
[Abstract]
[Full Text]
-
Fonseca, M. V., Escalante-Semerena, J. C.
(2001). An in Vitro Reducing System for the Enzymic Conversion of Cobalamin to Adenosylcobalamin. J. Biol. Chem.
276: 32101-32108
[Abstract]
[Full Text]
Copyright © 1993 by the American Society for Microbiology. All rights reserved.