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J Bacteriol. 1977 December; 132(3): 796-805
Copyright © 1977 American Society for Microbiology. All Rights Reserved.

Genetic Analysis of Components Involved in Vitamin B₁₂ Uptake in Escherichia coli

Philip J. Bassford Jr. and Robert J. Kadner

¹ Department of Microbiology, The University of Virginia School of Medicine, Charlottesville, Virginia 22901

ABSTRACT

The products of three genes are involved in cyanocobalamin (B₁₂) uptake in Escherichia coli. btuB (formerly bfe), located at min 88 on the Escherichia coli linkage map, codes for a protein component of the outer membrane which serves as receptor for B₁₂, the E colicins, and bacteriophage BF23. Four phenotypic classes of mutants varying in response to these agents were found to carry mutations that, based on complementation and reversion analyses, reside in the single btuB cistron. In one mutant class, ligand binding to the receptor appeared to be normal, but subsequent B₁₂ uptake was defective. The level of receptor and rate of uptake were responsive to btuB gene dosage. Previous studies showed that the tonB product was necessary for energy-dependent B₁₂ uptake but not for its binding. Other than those in tonB, no mutations that conferred insensitivity to group B colicins affected B₁₂ utilization. The requirement for the btuB and tonB products could be bypassed by elevated levels of B₁₂ (>1 µM) or by mutations compromising the integrity of the outer membrane as a permeability barrier. Utilization of elevated B₁₂ concentrations in strains lacking the btuB-tonB uptake system was dependent on the function of the btuC product. This gene was located at 37.7 min on the linkage map, with the order pps-btuC-pheS. Strains altered in btuC but with an intact btuB-tonB system were only slightly impaired in B₁₂ utilization, being defective in its accumulation. This defect was manifested as inability to retain B₁₂, such that intracellular label was almost completely lost by exchange or efflux. It is proposed that btuC encodes a transport system for B₁₂ in the periplasm.

Present address: Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston MA 02115.

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