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. 1970 Jan;101(1):127–132. doi: 10.1128/jb.101.1.127-132.1970

Catabolic Activities of Neisseria meningitidis: Utilization of Glutamate1

Louis P Mallavia a,2, Emilio Weiss a
PMCID: PMC250459  PMID: 4983643

Abstract

Glutamate was catabolized at a rapid rate by Neisseria meningitidis, group B. Surprisingly, there was a lag of 5 to 30 min in respiration, but not in CO2 production from C1, and an appreciable amount of succinate accumulated. The eventual rapid rate of respiration was not prevented by the addition of chloramphenicol. The lag period was eliminated by combinations of substrates that favored the activity of a glutamate-oxaloacetate transaminase. It is suggested that with glutamate as the sole substrate, the reaction terminated at succinate, required only moderate O2 uptake, and did not result in the transport of succinate to enzymatic sites. The lag period represented the time required for the accumulation of succinate and its transport to enzymatic sites by energy provided by the metabolism of the remaining glutamate. When the transaminase was operative, on the other hand, successive products of the reaction were immediately placed in contact with enzymatic sites.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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