1954
DOI: 10.1002/9780470122600.ch5
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Enzymic Mechanisms in the Citric Acid Cycle

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Cited by 18 publications
(3 citation statements)
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“…Differential expression was found for 15 proteins, including citrate synthase (2.3.3.1) [44], malate dehydrogenase, cyto, mdh5, aconitate hydratase (4.2.1.3), phosphoenolpyruvate carboxykinase, isocitrate dehydrogenase (NAD+) (1.1.1.41) [45, 46], the succinyl-CoA synthetase beta subunit (6.2.1.4/6.2.1.5) [47, 48] and the pyruvate dehydrogenase E1 component alpha/beta subunit (1.2.4.1) [49, 50]. Succinyl-CoA ligase and phosphoenolpyruvate carboxykinase showed decreased levels and belong to class 1.…”
Section: Resultsmentioning
confidence: 99%
“…Differential expression was found for 15 proteins, including citrate synthase (2.3.3.1) [44], malate dehydrogenase, cyto, mdh5, aconitate hydratase (4.2.1.3), phosphoenolpyruvate carboxykinase, isocitrate dehydrogenase (NAD+) (1.1.1.41) [45, 46], the succinyl-CoA synthetase beta subunit (6.2.1.4/6.2.1.5) [47, 48] and the pyruvate dehydrogenase E1 component alpha/beta subunit (1.2.4.1) [49, 50]. Succinyl-CoA ligase and phosphoenolpyruvate carboxykinase showed decreased levels and belong to class 1.…”
Section: Resultsmentioning
confidence: 99%
“…Citrate or 2-oxoglutaratedependent THNCoA reduction was most likely an artifact of the assay conditions, where 2-oxoglutarate served as indirect electron donor via oxidoreductase-mediated electron transfer, yielding NADH. Desulfobacterium strain N47 operates a modified citric acid cycle in which the ordinary 2-oxoglutarate dehydrogenase (38,39) is replaced by a 2-oxoglutarate:ferredoxin oxidoreductase (29). A similar oxidoreductase was also identified in strain NaphS2 (30).…”
Section: Discussionmentioning
confidence: 96%
“…Αυτή αποτελείται βασικως εκ τριών ενζύμων, τής πυροσταφυλικής άποκαρβοξυλάσης, τής λιποϊκής άκετυλοτρανσφεράσης και τής διϋδρολιποϊκής δεϋδρογενάσης. 41 , 153 Δια τήν εν λόγφ άντίδρασιν απαραίτητοι συνπαράγοντες, μεθ' ών σχηματίζονται ενδιάμεσα προϊόντα, είναι : Tò άκετυλ-CoA δρα ως συνπαράγων, ως άλλοστερικος ένεργοποιητής τοΰ ένζυμου, αυξάνοντας τήν δραστηριότητα του, διότι αυτή αυτή ή υπαρξις του όξαλοξεικοΰ οξέος είναι απαραίτητος δια τήν χρησιμοποίησιν του άκετυλ-CoA, προς σχηματισμόν του κιτρικού οξέος. Συνεπεία τούτου, όσον περισσότερον άκετυλ-CoA σχηματίζεται, τόσον περισσότερον όξαλοξεικόν απαιτείται, ό και επιτυγχάνεται κατόπιν της διεγερτικής δράσεως του πρώτου επί του ένζυμου.…”
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