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[Oxidation of Krebs cycle substrates by Eurytrema pancreaticum mitochondria].
Parazitologiia. 1977 Sep-Oct; 11(5):412-6.P

Abstract

From tissues of E. pancreaticum were isolated mitochondria capable to swell under the effect of some factors. The intensive oxidation of succinate, isocitrate, cisaconitate, oxalacetate and alpha-ketoglutarate by mitochondria and less intensive one of malate, fumarate, citrate and pyruvate were shown. NAD caused the rise in oxidation intensity of isocitrate, cis-aconitate, oxalacetate, alpha-ketoglutarate, malate, fumarate and pyruvate while NADP--of isocitrate and citrate.

Authors

Shestak EA
No affiliation info available

MeSH

Aconitic AcidAnimalsCitratesCitric Acid CycleDicrocoeliumFumaratesIn Vitro TechniquesIsocitratesKetoglutaric AcidsMalatesMitochondriaOxaloacetatesOxidation-ReductionPyruvatesSuccinates

Pub Type(s)

Journal Article

Language

rus

PubMed ID

909726

Citation

Shestak, E A.. "[Oxidation of Krebs Cycle Substrates By Eurytrema Pancreaticum Mitochondria]." Parazitologiia, vol. 11, no. 5, 1977, pp. 412-6.
Shestak EA. [Oxidation of Krebs cycle substrates by Eurytrema pancreaticum mitochondria]. Parazitologiia. 1977;11(5):412-6.
Shestak, E. A. (1977). [Oxidation of Krebs cycle substrates by Eurytrema pancreaticum mitochondria]. Parazitologiia, 11(5), 412-6.
Shestak EA. [Oxidation of Krebs Cycle Substrates By Eurytrema Pancreaticum Mitochondria]. Parazitologiia. 1977 Sep-Oct;11(5):412-6. PubMed PMID: 909726.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Oxidation of Krebs cycle substrates by Eurytrema pancreaticum mitochondria]. A1 - Shestak,E A, PY - 1977/9/1/pubmed PY - 1977/9/1/medline PY - 1977/9/1/entrez SP - 412 EP - 6 JF - Parazitologiia JO - Parazitologiia VL - 11 IS - 5 N2 - From tissues of E. pancreaticum were isolated mitochondria capable to swell under the effect of some factors. The intensive oxidation of succinate, isocitrate, cisaconitate, oxalacetate and alpha-ketoglutarate by mitochondria and less intensive one of malate, fumarate, citrate and pyruvate were shown. NAD caused the rise in oxidation intensity of isocitrate, cis-aconitate, oxalacetate, alpha-ketoglutarate, malate, fumarate and pyruvate while NADP--of isocitrate and citrate. SN - 0031-1847 UR - https://www.unboundmedicine.com/medline/citation/909726/[Oxidation_of_Krebs_cycle_substrates_by_Eurytrema_pancreaticum_mitochondria]_ DB - PRIME DP - Unbound Medicine ER -