A rapid quench kinetic study of ribulosebisphosphate carboxylase and in vitro modelling of resonant energy transfer between chlorophyll A solvated species in water/acetone solvent systems

  • Butcher, Karen Ann
Publication date
January 1989
Publisher
Purdue University (bepress)

Abstract

The net rate constants for conversion of substrate to intermediates to product of the ribulosebisphosphate carboxylase enzyme of Rhodospirillum rubrum were determined by fitting the equations corresponding to a sequential irreversible reaction to the levels of components from rapid kinetic quenches. The first intermediate of the reaction, the ene-diol of 1,5-ribulosebisphosphate, was detected as the monophosphate elimination product obtained upon acid quenching the enzymic reaction mixture and reduction of the products with sodium borohydride. Similarly, the second intermediate, carboxy-keto-arabinitolbisphosphate (CKABP), was detected as a mixture of 2$\sp\prime$- and 4-carboxyarabinitol 1,5-bisphosphate. Remaining substrate, ribulosebisph...

Extracted data

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