Affiliation:
1. Department of Microbiology, Naval Medical Research Institute, Bethesda, Maryland 20014
Abstract
Resting cell suspensions of
Neisseria meningitidis
group B (strain 2091) do not catabolize citrate as the sole substrate to an appreciable degree. When another substrate, such as glutamate, is also present to furnish energy for transport, citrate metabolism is greatly stimulated. Within limits, the amount of CO
2
produced from citrate is proportional to the amount of glutamate added. When the cells are disrupted, citrate is degraded at a rapid rate and the stimulatory effect of glutamate is completely eliminated. Pronounced stimulation of citrate metabolism by glutamate was demonstrated in 12 of 13 strains of
N. meningitidis
tested and only 1 of 6 strains of
N. lactamicus
. The remaining strains of
N. lactamicus
and one each of
N. gonorrhoeae, N. flavescens
, and
N. flava
did not utilize significant amounts of citrate in the absence or presence of glutamate.
N. catarrhalis
shared with
Mima polymorpha
and
Moraxella glucidolytica
a capability to catabolize citrate at a rapid rate without added glutamate. It is concluded that tests of glutamate-stimulated citrate metabolism may contribute to species characterization in the genus
Neisseria
.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
12 articles.
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