Genetic polymorphism of red cell glutamate-pyruvate transaminase in Japanese

Six hundred and eight red cell hemolysates were screened for glutamate-pyruvate transaminase (GPT) by means of isoelectric focusing. Two new variant phenotypes were detected, neither of which could be distinguished from GPT2-1 and GPT2 by conventional starch gel electrophoresis. The two types were considered to correspond to GPT2B-1 and GPT2A-2C reported previously in samples of European origin.     

Identification of human red cell glutamate-pyruvate transaminase (GPT) phenotypes by isoelectric focusing.

Isoenzymes of human red cell glutamate-pyruvate transaminase (GPT) were resolved by isoelectric focusing (IEF) of hemolysates in polyacrylamide gels at pH 5.0-7.0. The bands of enzyme activity required both alpha-ketoglutarate and L-alanine in the staining mixture for visualization, indicating that the bands were not lactate dehydrogenase or glutamate dehydrogenase. Phenotyping of 41 individuals by IEF, including types GPT 1, 2A, 1-2A, 1-2B, and 2A-2B, agreed with the typing results obtained by electrophoresis in starch gels and in polyacrylamide gels at acid and alkaline pH. Analysis of one kindred demonstrated autosomal codominant transmission of the rare GPT*2B gene through 3 generations. IEF facilitates phenotyping by permitting identification of the GPT types on a single gel with a considerable reduction in time and cost. Although no new variants were found in this investigation, IEF may be more powerful for the recognition of presently undetected variants of GPT.     

The determination of the red cell isoenzymes 6-phosphogluconate dehydrogenase (E.C.1.1.1.44) and acid phosphatase (E.C.3.1.3.2) by means of agarosegel thinlayer electrophoresis (author's transl)

Methods for the determination of the red cell isoenzymes 6-PGD and acP by means of agarosegel thinlayer electrophoresis are referred. Using these relatively simple techniques, results can be obtained after at least two hours. The quality of separation in both systems is higher than that obtained after starch gel electrophoresis.     

Population genetics of red cell glyoxalase I (E.C.: 4.4.1.5)

Summary The polymorphism of Glyoxalase I was investigated in a population sample from Southwestern Germany. The frequency of the GLO² allele was determined to be 0.427.

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Zusammenfassung Der Polymorphismus der Glyoxalase I wurde an einer Bevölkerungsstichprobe aus Südwestdeutschland untersucht. Die Genhäufigkeit für GLO¹ beträgt 0,427.

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Supported by the Deutsche Forschungsgemeinschaft.     

Aldehyde oxidase isoenzymes (E.C. 1.2.3.1) in potato tubers (Solanum tuberosum)

Two isoenzymes of aldehyde oxidase (E.C. 1.2.3.1 [EC] ) can be separatedfrom potato tubers (Solanum tuberosum) by polyacrylamide gelelectrophoresis. The pH optima of these two isoenzymes werepH 7.5. Both enzymes can oxidize different aldehydes, e.g. crotonaldehyde,Propionaldehyde, acetaldehyde, formaldehyde, glyoxal and benzyl-aldehyde.The isoenzymes could not use xanthine as a substrate. Formaldehydewas oxidized only in the presence of phosphate ions. A substratedependent inhibition of the enzyme activity is possible throughchloral hydrate. PMS, FMN, riboflavine, cytochrome c and O₂ serve as electronacceptors. (Received December 12, 1973; )     

Screening for thermostability and electrophoretic red blood cell sorbitol dehydrogenase (E.C.1.1.1.14) variants

A screening for both thermostability and electrophoretic red blood cell sorbitol dehydrogenase (RBC-SORD) variants in blood donors was performed. SORD activity in standard conditions (unheated samples) in 274 individuals was 198 +/- 38.6 mIU/g Hb. The ratio of enzymatic activity after heating (H) to the activity in controls (C) before heating (H/C ratio) was 0.39 +/- 0.10. H/C ratios minor than 0.1 in 3 out of 274 blood donors and higher than 0.9 in 1 were observed. In 208 individuals, four electrophoretic phenotypes were observed: I) Three bands, named a, b and c, with cathodic mobility in 163 individuals (78.36%); II) Two bands a and c in 25 individuals (12.02%); III) Two bands b and c in 14 (6.73%); and IV) One band, c in 6 (2.88%). Studies carried out to characterize the three bands suggest that they are isozymes of the same locus with the observation of an interchange of the bands as a normal phenomena.     

Population genetics of soluble glutamic-pyruvic transaminase (EC:2.6.1.2): Gene frequencies in Southwestern Germany

Summary In a population sample from Southwestern Germany GPT-phenotypes have been determined. The allele GPT¹ is more frequent in this sample than in the USA.Supported by the Deutsche Forschungsgemeinschaft.     

Transspecific variability of glutamic oxaloacetic transaminase (E.C. 2.6.1.1.) in Primates

Summary The genetic polymorphism of soluble and mitochondrial glutamic oxaloacetic transaminase has been investigated in Primates. 3 variants of the soluble enzyme and 2 variants of the mitochondrial enzyme could be demonstrated. The distribution of the various phenotypes has been estimated.

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Zusammenfassung Die Glutamat-Oxalacetat-Transaminasen der Primaten, zeigen eine genetisch determinierte Variabilität. Es konnten 3 cytoplasmatische und 2 mitochondriale Enzymvarianten nachgewiesen werden. Die Verteilung der Phänotypen wurde ermittelt.

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Direktor: Prof. Dr. Dr. H. Ritter

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Supported by the Deutsche Forschungsgemeinschaft.     

Population genetics of red cell glyoxalase I (E.C.:4.4.1.5): Gene frequencies in southwestern Germany.

The polymorphism of Glyoxalase I was investigated in a population sample from Southweatern Germany. The frequency of the GLO-2 allele was determined to be 0.427.     

Population genetics of red cell phosphoglucomutase (E C 2.7.5.1): Gene frequencies in Southwestern Germany

Summary In a population sample from Southwestern Germany PGM₁-phenotypes are determined. The gene frequencies fit well to those of Great Britain.Head: Prof. Dr. Dr. H. BaitschSupported by the Deutsche Forschungsgemeinschaft.