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Clinical Chemistry, Vol 21, 730-734, Copyright © 1975 by the American Association for Clinical Chemistry
1 Department of Biochemistry, Michael Reese Hospital and Medical Center, Chicago, Ill. 60616.
We describe a procedure for enzymatic assay of citrate
in human serum. The citrate is degraded to acetate and
oxaloacetate with citrate oxaloacetate-lyase (pro-3S-CH2 · COO-
acetate) (EC 4.1.3.6). Some oxaloacetate loses CO2 to form pyruvate. Addition of malate and
lactate dehydrogenases (EC 1.1.1.37 and 1.1.1.27) permits determination of the oxaloacetate and pyruvate
generated, and thus of the citrate concentration. The
decrease in NADH concentration is measured fluorometrically. Results obtained for 30 consecutive human sera
by this procedure were compared to the procedure in
which the citrate is converted to pentabromoacetone.
There was no statistically significant difference in values
obtained by the two procedures. The range of values
(mean ± 2 SD) found for sera from 25 blood donors by
this procedure was 12.8-27.2 mg/liter (mean, 19.0
mg/ liter). Serum citrate as measured by both procedures during a glucose tolerance test was decreased
from initial values under the influence of administered
glucose (and endogenous insulin). Insulin concentrations
were also measured during these glucose-tolerance
tests. Citrate concentrations remain subnormal after the
glucose and insulin concentrations return to their initial
values. This accords with published reports.
Submitted on January 9, 1975
Accepted on February 24, 1975
The following articles in journals at HighWire Press have cited this article:
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J. Lin, J. S. Hogan, and K. L. Smith Antigenic Homology of the Inducible Ferric Citrate Receptor (FecA) of Coliform Bacteria Isolated from Herds with Naturally Occurring Bovine Intramammary Infections Clin. Vaccine Immunol., November 1, 1999; 6(6): 966 - 969. [Abstract] [Full Text] [PDF] |
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