Gd. Nanos et al., RESPIRATORY METABOLISM OF PEAR FRUIT AND CULTURED-CELLS EXPOSED TO HYPOXIC ATMOSPHERES - ASSOCIATED CHANGE IN ACTIVITIES OF KEY ENZYMES, Journal of the American Society for Horticultural Science, 119(2), 1994, pp. 288-294
'Bartlett' pears (Pyrus communis L.) at two physiological stages, clim
acteric minimum or approaching the climacteric peak as achieved via st
orage for 2 or 8 weeks in air at 0C, respectively, were either ripened
at 20C in air immediately or after exposure to 0.25 % O-2 for 4 days
at 20C. Fruit stored for 2 weeks had relatively stable phosphofructoki
nase (PFK), pyrophosphate : fru-6-P phosphotransferase (PFP), and pyru
vate kinase (PK) activities but decreasing succinate dehydrogenase (SD
H) activities during ripening in air. Similar fruit treated with 0.25%
O-2 had slightly increased PFK, PFP, and SDH activities and decreased
PK activity. Fruit stored for 8 weeks exhibited higher levels of PFK
and PFP activity upon transfer to 20C, in accordance with their more a
dvanced physiological state. In general, the enzymic changes in these
fruit upon exposure to 0.25% O-2 and subsequent ripening in air were s
imilar to those observed in the less-mature counterparts, most notable
being an increase in mitochondrial SDH. Exposure of suspension-cultur
ed pear fruit cells' to hypoxia resulted in an accentuated rise in pho
sphoenolpyruvate carboxykinase activity and a dramatic rise in SDH act
ivity upon transfer to air. Taken in concert, the enzymic analysis sup
ports the hypothesis that the rise in succinate levels observed in hyp
oxic fruit tissues is the result of a partial reductive tricarboxylic
acid cycle. Cytochrome oxidase activity did not change during hypoxia
whereas soluble peroxidase decreased somewhat, perhaps a reflection of
their Michaelis constants for O-2.