By Roland A. Coulson, Thomas Hernandez
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Extra info for Alligator Metabolism Studies on Chemical Reactions in Vivo
1. 4. To convert 0 2 usage to glucose oxidation, divide the μτηο\ of glucose used by 6. 56 μηιοΐ/ml). 047 ml/g/min for the entire body and 2/3 that per gram for resing muscle. It is assumed that 0 2 consumption of muscle working maximally increases 30-fold over that used at rest. Í This represents a "corrected" rate of blood flow for the alligator. The actual rate would be about twice these figures to compensate for a low blood hemoglobin (see text). These values are for a 700 kg alligator. * At any one substrate concentration, the velocity of a reaction will be proportional to the A-V difference, and the quantity reacted during unit time will be the A-V difference times the blood flow (F).
1 mmol/g/min. 5 mmol/g/min. In other words, the dry weight of the glucose absorbed/min would approach half the dry weight of the transporting mucosa of the small intes tine. It would be difficult not to conclude that the ex pression for transport of a food metabolite across the gut mucosa or across other cell membranes should resemble that for enzyme reactions generally. If trans port involves a carrier molecule, the rate of formation of the complex, and the subsequent rate of its break down should be proportional to blood flow and to the substrate concentration.
Let us next assume that in deamination of amino acid A either the formation of the £ 5 complex or its breakdown is indeed rate-limiting at any one blood flow rate but that the actual velocity of the rate-limit ing reaction has no upper limit since it may be in creased by increasing the blood flow. N o w if one of the reactions is also rate-limiting (at the same blood flow) in the deamination of a second amino acid, B, but the rate constant Κ for the rate-limiting reaction of Β is half that of A, increasing the blood flow will increase the rate of deamination of both amino acids without limit, but amino acid A will still be deaminated twice as fast as B.