An endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes has been identified.
First-pass extracted concept
endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes
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The activity can be released from isolated thylakoid membranes by high-NaCl washing and reconstituted by readdition of desalted wash supernatant.
Quoted textsource-backed
The activity can be released from isolated thylakoid membranes by washing with high concentrations of NaCl and reconstituted by readdition of the desalted wash supernatant.
The proteolytic activity can be released from isolated thylakoid membranes by high-salt washing and reconstituted by readdition of the desalted wash supernatant.
Quoted textsource-backed
The activity can be released from isolated thylakoid membranes by washing with high concentrations of NaCl and reconstituted by readdition of the desalted wash supernatant.
The proteolytic process is strictly dependent on ATP.
Quoted textsource-backed
The proteolytic process is strictly dependent on ATP
The proteolytic process is strictly dependent on ATP.
Quoted textsource-backed
The proteolytic process is strictly dependent on ATP
After initiation by high-intensity light, LHCII degradation can occur in complete darkness.
Quoted textsource-backed
Once initiated by high-intensity light, the degradation of LHCII can readily occur in complete darkness.
The protease involved is of the serine or cysteine type.
Quoted textsource-backed
the protease involved is of the serine or cysteine type
The protease involved is of the serine or cysteine type.
Quoted textsource-backed
the protease involved is of the serine or cysteine type
After in vivo induction, the proteolysis can be followed in vitro in isolated intact chloroplasts and thylakoid membranes.
Quoted textsource-backed
The proteolysis can, after induction in vivo, be experimentally followed in vitro, both in isolated intact chloroplasts and thylakoid membranes.
After in vivo induction, the proteolysis can be followed in vitro in isolated intact chloroplasts and thylakoid membranes.
Quoted textsource-backed
The proteolysis can, after induction in vivo, be experimentally followed in vitro, both in isolated intact chloroplasts and thylakoid membranes.
The identified enzymic activity is involved in degradation of LHCII in response to increased irradiance.
Quoted textsource-backed
This enzymic activity is involved in the degradation of the major light-harvesting chlorophyll a/b protein of photosystem II (LHCII) in response to exposure of leaves to increased irradiance.
The identified enzymic activity is involved in degradation of LHCII in response to increased irradiance.
Quoted textsource-backed
This enzymic activity is involved in the degradation of the major light-harvesting chlorophyll a/b protein of photosystem II (LHCII) in response to exposure of leaves to increased irradiance.
An endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes was identified.
Quoted textsource-backed
An endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes has been identified.
An endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes was identified.
Quoted textsource-backed
An endogenous proteolytic activity associated with spinach chloroplast thylakoid membranes has been identified.
Proteolysis of LHCII requires an induction period and is detectable 48-72 hours after transfer from low-intensity to high-intensity light.
Quoted textsource-backed
This proteolysis of LHCII requires an induction period and can only be detected 48-72 hours after transfer of the plants from low-intensity to high-intensity light.
After initiation by high-intensity light, LHCII degradation can occur in complete darkness.
Quoted textsource-backed
Once initiated by high-intensity light, the degradation of LHCII can readily occur in complete darkness.
The protease is concluded to be extrinsically bound to the outer surface of the stroma-exposed regions of the stacked thylakoid membrane.
Quoted textsource-backed
It is concluded that the protease is extrinsically bound to the outer surface of the stroma-exposed regions of the stacked thylakoid membrane.
The protease is concluded to be extrinsically bound to the outer surface of the stroma-exposed regions of the stacked thylakoid membrane.
Quoted textsource-backed
It is concluded that the protease is extrinsically bound to the outer surface of the stroma-exposed regions of the stacked thylakoid membrane.
Proteolysis of LHCII requires an induction period and is detectable only 48-72 hours after transfer from low-intensity to high-intensity light.
Quoted textsource-backed
This proteolysis of LHCII requires an induction period and can only be detected 48-72 hours after transfer of the plants from low-intensity to high-intensity light.