Although it is generally assumed that the plastoquinone pool of thylak
oid membranes in leaves of higher plants is rapidly oxidized upon dark
ening, this is often not the case. A multiflash kinetic fluorimeter wa
s used to monitor the redox state of the plastoquinone pool in leaves.
It was found that in many species of plants, particularly those using
the NAD-malic enzyme C4 system of photosynthesis, the pool actually b
ecame more reduced following a light to dark transition. In some Amara
nthus species, plastoquinone remained reduced in the dark for several
hours. Far red light, which preferentially drives Photosystem I turnov
er, could effectively oxidize the plastoquinone pool. Plastoquinone wa
s re-reduced in the dark within a few seconds when far red illuminatio
n was removed. The underlying mechanism of the dark reduction of the p
lastoquinone pool is still uncertain but may involve chlororespiratory
activity.