Affiliation:
1. Department of Microbiology and Immunology, University of Oregon Health Sciences Center, Portland, Oregon 97201
Abstract
The binding of [1,2-
3
H]progesterone to progesterone-sensitive
Neisseria gonorrhoeae
CS-7 and the progesterone-insensitive
Neisseria mucosa, Pseudomonas aeruginosa
, and
Salmonella typhimurium
(rough and smooth strains) was investigated. The kinetics of binding to
N. gonorrhoeae
CS-7 demonstrated that the majority of the progesterone binding occurred and equilibrium was reached within the first 30 min. Despite the rapid binding of progesterone, only about 20% of the added steroid was bound at the cell concentration used throughout this study. Whole cells of progesterone-insensitive bacteria bound progesterone less efficiently than the progesterone-sensitive
N. gonorrhoeae
CS-7.
N. mucosa
bound low amounts of this steroid (20% of that bound by
N. gonorrhoeae
CS-7) whereas the other gram-negative bacteria exhibited little progesterone binding (<3% of that bound by
N. gonorrhoeae
CS-7). The outer membrane permeability of
N. gonorrhoeae
CS-7, as measured by crystal violet uptake and inhibition, was similar to the deep rough mutant of
S. typhimurium
TA 1535. The latter organism neither bound nor was inhibited by progesterone. However, isolated cell envelopes of
N. gonorrhoeae
and progesterone-insensitive bacteria all bound progesterone equally well. Cortisone and cholesterol, althouh structurally similar to progesterone, were not inhibitory to
N. gonorrhoeae
and did not bind to whole cells as well as progesterone. The major site of progesterone binding appeared to be the cytoplasmic membrane, which bound four times more progesterone than the outer membrane. In addition, isolated cytoplasmic membrane proteins bound more than three times more progesterone per milligram of protein than the intact membrane.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
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