Abstract
Shigella flexneri strains were assayed for the ability to synthesize and utilize phenolate and hydroxamate siderophores. The hydroxamate aerobactin was synthesized by all isolates tested, whereas phenolates were only rarely produced. Expression of aerobactin was accompanied by production of a single iron-regulated outer membrane protein (M(r) = 74,000). This protein was not produced by a mutant defective in aerobactin utilization and may serve as the aerobactin receptor. Phenolate (enterobactin)-producing strains synthesized three additional outer membrane proteins (M(r) = 74,000, 81,000, and 83,000) in response to iron starvation. These proteins are the same apparent size as those produced by Escherichia coli K-12 strains. Ent sequences are apparently present in strains which do not synthesize this compound. Although normally silent, ent genes can be activated in Ent- strains to produce Ent+ variants. These laboratory variants are phenotypically indistinguishable from clinical Ent+ isolates.
Original language | English (US) |
---|---|
Pages (from-to) | 949-955 |
Number of pages | 7 |
Journal | Journal of Bacteriology |
Volume | 155 |
Issue number | 3 |
State | Published - 1983 |
Externally published | Yes |
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ASJC Scopus subject areas
- Applied Microbiology and Biotechnology
- Immunology
Cite this
Expression of hydroxamate and phenolate siderophores by Shigella flexneri. / Payne, S. M.; Niesel, David; Peixotto, S. S.; Lawlor, K. M.
In: Journal of Bacteriology, Vol. 155, No. 3, 1983, p. 949-955.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Expression of hydroxamate and phenolate siderophores by Shigella flexneri
AU - Payne, S. M.
AU - Niesel, David
AU - Peixotto, S. S.
AU - Lawlor, K. M.
PY - 1983
Y1 - 1983
N2 - Shigella flexneri strains were assayed for the ability to synthesize and utilize phenolate and hydroxamate siderophores. The hydroxamate aerobactin was synthesized by all isolates tested, whereas phenolates were only rarely produced. Expression of aerobactin was accompanied by production of a single iron-regulated outer membrane protein (M(r) = 74,000). This protein was not produced by a mutant defective in aerobactin utilization and may serve as the aerobactin receptor. Phenolate (enterobactin)-producing strains synthesized three additional outer membrane proteins (M(r) = 74,000, 81,000, and 83,000) in response to iron starvation. These proteins are the same apparent size as those produced by Escherichia coli K-12 strains. Ent sequences are apparently present in strains which do not synthesize this compound. Although normally silent, ent genes can be activated in Ent- strains to produce Ent+ variants. These laboratory variants are phenotypically indistinguishable from clinical Ent+ isolates.
AB - Shigella flexneri strains were assayed for the ability to synthesize and utilize phenolate and hydroxamate siderophores. The hydroxamate aerobactin was synthesized by all isolates tested, whereas phenolates were only rarely produced. Expression of aerobactin was accompanied by production of a single iron-regulated outer membrane protein (M(r) = 74,000). This protein was not produced by a mutant defective in aerobactin utilization and may serve as the aerobactin receptor. Phenolate (enterobactin)-producing strains synthesized three additional outer membrane proteins (M(r) = 74,000, 81,000, and 83,000) in response to iron starvation. These proteins are the same apparent size as those produced by Escherichia coli K-12 strains. Ent sequences are apparently present in strains which do not synthesize this compound. Although normally silent, ent genes can be activated in Ent- strains to produce Ent+ variants. These laboratory variants are phenotypically indistinguishable from clinical Ent+ isolates.
UR - http://www.scopus.com/inward/record.url?scp=0020525402&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0020525402&partnerID=8YFLogxK
M3 - Article
C2 - 6224775
AN - SCOPUS:0020525402
VL - 155
SP - 949
EP - 955
JO - Journal of Bacteriology
JF - Journal of Bacteriology
SN - 0021-9193
IS - 3
ER -