Literature DB >> 13910213

Mutation to neostigmine resistance in a cholinesterase-containing Pseudomonas.

B W SEARLE, A GOLDSTEIN.   

Abstract

Searle, Barbara W. (Stanford University School of Medicine, Palo Alto, Calif.) and Avram Goldstein. Mutation to neostigmine resistance in a cholinesterase-containing Pseudomonas. J. Bacteriol. 83:789-796. 1962.-In a strain of Pseudomonas fluorescens containing an inducible cholinesterase, the activity of that enzyme is rate-limiting for growth when acetyl-choline is the sole source of carbon or nitrogen. Under these circumstances, neostigmine, a cholinesterase inhibitor, becomes a growth inhibitor.A neostigmine-resistant mutant was isolated, and the properties of its cholinesterase were compared with those of the wild-type enzyme. There were no differences in penetration of cells by inhibitor, rate of enzyme-inhibitor combination, affinity of inhibitor or substrate for the cholinesterase, or protective effect of substrate upon the enzyme. However, the mutant consistently formed cholinesterase at about twice the wild-type rate. Mutation, in this case, appears to result in a specific change in the differential rate of enzyme biosynthesis. The relationship of this change to neostigmine resistance is discussed, and it is suggested that the effect observed here may be prototypic of a general type of mechanism responsible for acquired drug resistance.

Entities:  

Keywords:  CHOLINESTERASE/metabolism; NEOSTIGMINE/pharmacology; PSEUDOMONAS/genetics

Mesh:

Substances:

Year:  1962        PMID: 13910213      PMCID: PMC279357          DOI: 10.1128/jb.83.4.789-796.1962

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  11 in total

1.  Induction of cholinesterase biosynthesis in Pseudomonas fluorescens.

Authors:  D B GOLDSTEIN
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3.  Enzymatic basis of resistance to aureomycin. I. Differences between flavoprotein nitro reductases of sensitive and resistant Escherichia coli.

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4.  Studies on the enzymatic formation of citrovorum factor by Streptococcus faecalis.

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Journal:  J Biol Chem       Date:  1953-05       Impact factor: 5.157

5.  Resistance to folic acid analogues in a strain of Streptococcus faecalis.

Authors:  C A NICHOL; S F ZAKRZEWSKI; A D WELCH
Journal:  Proc Soc Exp Biol Med       Date:  1953-06

6.  An adaptive bacterial cholinesterase from a Pseudomonas species.

Authors:  D B GOLDSTEIN; A GOLDSTEIN
Journal:  J Gen Microbiol       Date:  1953-02

7.  A colorimetric method for the determination of choline and acetylcholine in small amounts.

Authors:  F J Beattie
Journal:  Biochem J       Date:  1936-09       Impact factor: 3.857

8.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

9.  Properties and behavior of purified human plasma cholinesterase. III. Competitive inhibition by prostigmine and other alkaloids with special reference to differences in kinetic behavior.

Authors:  A GOLDSTEIN
Journal:  Arch Biochem Biophys       Date:  1951-11       Impact factor: 4.013

10.  Replica plating and indirect selection of bacterial mutants.

Authors:  J LEDERBERG; E M LEDERBERG
Journal:  J Bacteriol       Date:  1952-03       Impact factor: 3.490

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