Honeybee flight muscle phosphoglucose isomerase: matching enzyme capacities to flux requirements at a near-equilibrium reaction

نویسندگان

  • Staples
  • Suarez
چکیده

In honeybee flight muscle, there are close matches between physiological flux rates and the maximal activities (Vmax; determined using crude homogenates) of key enzymes catalyzing non-equilibrium reactions in carbohydrate oxidation. In contrast, phosphoglucose isomerase (PGI), which catalyzes a reaction believed to be close to equilibrium, occurs at Vmax values greatly in excess of glycolytic flux rates. In this study, we measure the Vmax of flight muscle PGI, the kinetic parameters of the purified enzyme, the apparent equilibrium constants for the reaction and the tissue concentrations of substrate and product. Using the Haldane equation, we estimate that the forward flux capacity (Vf) for PGI required to achieve physiological glycolytic flux rates is between 800 and 1070 units ml-1 cell water, approximately 45­60 % of the empirically measured Vmax of 1770 units ml-1 cell water at optimal pH (8.0) and low ionic strength (no added KCl). When measured at physiological pH (7.0) and ionic strength (120 mmol l-1 KCl) with saturating levels of substrate, PGI activity is 1130 units ml-1 cell water, a value close to the calculated Vf. These results reveal a very close match between predicted and measured PGI flux capacities, and support the concept of an economical design of muscle metabolism in systems working at very high metabolic rates.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Flux control and excess capacity in the enzymes of glycolysis and their relationship to flight metabolism in Drosophila melanogaster.

An important question in evolutionary and physiological genetics is how the control of flux-base phenotypes is distributed across the enzymes in a pathway. This control is often related to enzyme-specific levels of activity that are reported to be in excess of that required for demand. In glycolysis, metabolic control is frequently considered vested in classical regulatory enzymes, each strongl...

متن کامل

Isolation of Crystalline Phosphoglucose Isomerase from Brewers' Yeast.

In a program to elucidate the mechanism by which phosphoglucose isomerasel participates in the catalyzed isomerization between glucose 6-phosphate and fructose g-phosphate, isolation of the enzyme from several sources is pursued as the basis for quantitative studies of its protein nature. The comparative investigation of several heteroenzymes appears to be a valuable tool in identifying the str...

متن کامل

Disequilibrium in the triose phosphate isomerase system in rat liver.

1. The equilibrium constant at 38 degrees and I 0.25 of the triose phosphate isomerase reaction was found to be 22.0 and that of the aldolase reaction, 0.99x10(-4)m. The [dihydroxyacetone phosphate]/[glyceraldehyde phosphate] ratio was found to be 9.3 in rat liver. The causes of the apparent deviation of the triose phosphate isomerase system from equilibrium in vivo have been investigated. 2. T...

متن کامل

The effect of pH and temperature on the kinetic parameters of phosphoglucose isomerase. Participation of histidine and lysine in a proposed dual function mechanism.

Phosphoglucose isomerase (D-glucose-6-phosphate ketolisomerase, EC 5.3.1.9) from rabbit skeletal muscle has been subjected to a detailed kinetic study of the effect of pH and temperature on the Michaelis constants, the maximal velocities, the dissociation constant for the competitive inhibitor 6-phosphogluconate, and the equilibrium constant of the reaction. A coupled pH-stat assay was establis...

متن کامل

Bifunctional phosphoglucose/phosphomannose isomerases from the Archaea Aeropyrum pernix and Thermoplasma acidophilum constitute a novel enzyme family within the phosphoglucose isomerase superfamily.

The hyperthermophilic crenarchaeon Aeropyrum pernix contains phosphoglucose isomerase (PGI) activity. However, obvious homologs with significant identity to known PGIs could not be identified in the sequenced genome of this organism. The PGI activity from A. pernix was purified and characterized. Kinetic analysis revealed that, unlike all known PGIs, the enzyme catalyzed reversible isomerizatio...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of experimental biology

دوره 200 Pt 8  شماره 

صفحات  -

تاریخ انتشار 1997