Week 7 GTP Metabolisum

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14 Terms

1
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Q: What are the three main precursors for gluconeogenesis?

Oxaloacetate, lactate, and amino acids.

2
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Which enzyme converts pyruvate to oxaloacetate in gluconeogenesis, and where does this occur?

Pyruvate carboxylase occurs in the mitochondria and requires ATP.

3
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What enzyme converts oxaloacetate to phosphoenolpyruvate (PEP), and what energy source does it require?

PEP carboxykinase (PEPCK); it requires GTP.

4
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Which enzymes bypass the irreversible steps of glycolysis in gluconeogenesis?

Pyruvate carboxylase, PEPCK, fructose 1,6-bisphosphatase, and glucose 6-phosphatase.

5
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Where do the steps of gluconeogenesis occur within the cell?

Initial steps (e.g., pyruvate to oxaloacetate) in the mitochondria; later steps in the cytoplasm.

6
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Why does gluconeogenesis require ATP and GTP?

To overcome the energy barriers of glycolysis’s irreversible steps; it's an energy-consuming process.

7
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Under what conditions is gluconeogenesis upregulated?

During fasting, low blood glucose, or carbohydrate deprivation.

8
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What is required to "activate" fatty acids before oxidation, and where does this happen?

Coenzyme A (CoA), via acyl-CoA synthetase in the cytoplasm.

9
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What is the purpose of fatty acid oxidation (beta-oxidation)?

To break down fatty acids into acetyl-CoA, which enters the citric acid cycle for energy production.

10
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How are fatty acids transported into the mitochondria after activation?

Via the carnitine shuttle system (though not detailed, be aware it's needed for mitochondrial entry).

11
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What role does acetyl-CoA play in metabolism?

It links fatty acid oxidation to the citric acid cycle and contributes to NADH/FADH2 production.

12
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What are the major components of the electron transport chain (ETC)?

Complexes I–IV, electron carriers (NADH, FADH2), and ATP synthase (Complex V).

13
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How does the ETC produce ATP?

By pumping protons to create a gradient used by ATP synthase in oxidative phosphorylation.

14
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What are the main energy storage molecules in the body, and where are they stored?

Glycogen (in liver and muscle) for short-term energy; protein (in muscle) for longer-term energy.