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Pepsi [2]
3 years ago
7

Which process is catalyzed by rubisco during the light-independent reactions of photosynthesis?

Biology
2 answers:
irina1246 [14]3 years ago
8 0

Answer:

The correct is the carboxylation process.

Explanation:

Rubisco or ribulose-1,5-bisphosphate carboxylase/oxygenase is the major enzyme of the calvin cycle. It is responsible for the fixation of carbon dioxide in plants into energy-rich molecules by initiating the Calvin cycle. The chlorophyll captured solar light at the origin of the processes of photosynthesis. RuBP or rubisco catalyzes both carboxylation and oxidation of ribulose-1,5-bisphosphate.

Thus, the correct answer is the carboxylation process.

son4ous [18]3 years ago
7 0
<span>RuBisCO enzyme catalyzes the carboxylation of ribulose-1,5-bisphosphate during the CO2 fixation in the first stage of light-independent reactions.

</span><span>The light-independent reactions are the second stage of photosynthesis, also called dark reactions because they are not directly driven by light. These reactions convert carbon dioxide (CO2) and other compounds into glucose. 
Read more on Brainly.com - brainly.com/question/9262287#readmore
</span>
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DCCD (dicyclohexylcarbodiimide) inhibits oxidative phosphorylation when the substrate is mitochondrial NADH. DCCD is a drug that
VARVARA [1.3K]

Answer:

A) Decreases cellular energy production

B) DCCD also affects K+ transport

Explanation:

A) Consequences are of DCCD on cellular energy production: <em>Decreases cellular energy production</em>

ATP-synthase pump is composed of two subunits: F1 catalytic subunit that synthesizes ATP, and F0 proton pumping subunits, that transport H+ through the membrane. F1 subunit might act independently of F0 to produce ATP, but this molecule can not be released without H+ gradient, which generates a movement necessary for ATP release from the catalytic center.

When any of the parts composing F0 react with DCCD, the subunit can not transport H+ through the membrane. DCCD inhibits the enzyme activity by blocking the protons´ flow.

As DCCD blocks the protons´ flow, and the protons´ flow is necessary to release the ATP molecule from the F1 subunit, no other ADP + Pi can enter to F1 subunit, and the production of ATP stops.

B) Other cellular effects of DCCD

There seem to be other effects of DCCD on cell activity, some of which are still under study. To name a few:

  • Diimide from DCCD seems to stimulate cytochrome b reduction and inhibits its reoxidation by ferricyanide.
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  • Inhibition of ubiquinol-cytochrome c reductase activity when exposing the cell to high concentrations of DCCD.
  • Inhibition of K+ transport, associated with the inhibition of H+ transport.

Concerning the effect of DCCD on the K+ transport, DCCD stops the extrusion of H+ and the consequent intrusion of K+.

DCCD strongly inhibits the simultaneous flow of H+ and K+. First, it inhibits H+ flow, acidification of the environment stops, but at this point, K+ keeps moving through the membrane. Once the H+ flow has ceased, the K+ flow slowly decreases until it finally stops moving. There is a lag time in the DCCD effect on K+ flow to the instantaneous effect on H+ flow.

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