题目 1 · Long Free-Response
9 分Photosynthetic organisms convert light energy into chemical energy through light-dependent reactions in the thylakoid membranes of chloroplasts. During this process, electrons are extracted from water and transported through a series of protein complexes (Photosystem II, the cytochrome \(b_6f\) complex, and Photosystem I) to reduce \(\text{NADP}^+\) to \(\text{NADPH}\), while simultaneously establishing a proton gradient used by ATP synthase to produce ATP.
Researchers are investigating the mechanism of action of a newly developed agricultural compound, Algicide-7 (A-7), on the photosynthetic electron transport chain of the unicellular green alga Chlorella vulgaris. Intact thylakoids were isolated from C. vulgaris cells and incubated in a buffered solution containing \(\text{ADP}\), inorganic phosphate (\(\text{P}_i\)), and oxidized electron acceptors. Samples were exposed to constant illumination (\(400\ \mu\text{mol photons}\cdot\text{m}^{-2}\cdot\text{s}^{-1}\)) at \(22^\circ\text{C}\) under various conditions. In Treatment 4, the artificial electron acceptor DCPIP was added; DCPIP accepts electrons directly from the primary electron acceptor of Photosystem II (PSII) before they reach the cytochrome \(b_6f\) complex. Rates of oxygen evolution, ATP synthesis, and \(\text{NADPH}\) production were measured and recorded in Table 1.
TABLE 1. RATES OF PHOTOSYNTHETIC ACTIVITY IN ISOLATED THYLAKOIDS UNDER VARYING EXPERIMENTAL TREATMENTS
| Treatment | Experimental Conditions | Rate of \(\text{O}_2\) Evolution (\(\mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) | Rate of ATP Synthesis (\(\mu\text{mol ATP}\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) | Rate of \(\text{NADPH}\) Formation (\(\mu\text{mol NADPH}\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) |
| :--- | :--- | :--- | :--- | :--- |
| 1 | No A-7, \(\text{NADP}^+\) present, Light | \(142 \pm 6\) | \(280 \pm 12\) | \(138 \pm 5\) |
| 2 | \(5\ \mu\text{M}\) A-7, \(\text{NADP}^+\) present, Light | \(71 \pm 4\) | \(140 \pm 8\) | \(69 \pm 4\) |
| 3 | \(20\ \mu\text{M}\) A-7, \(\text{NADP}^+\) present, Light | \(8 \pm 2\) | \(15 \pm 3\) | \(7 \pm 2\) |
| 4 | \(20\ \mu\text{M}\) A-7 + DCPIP, No \(\text{NADP}^+\), Light | \(140 \pm 7\) | \(22 \pm 4\) | \(0 \pm 0\) |
| 5 | No A-7, \(\text{NADP}^+\) present, Dark | \(0 \pm 0\) | \(0 \pm 0\) | \(0 \pm 0\) |
(a)
(i) Describe the biological function of water (\(\text{H}_2\text{O}\)) photolysis in the thylakoid lumen during the light-dependent reactions of photosynthesis.
(ii) Explain how the transfer of electrons along the photosynthetic electron transport chain establishes a proton concentration gradient across the thylakoid membrane.
(b)
(i) Identify the dependent variable measured to assess Photosystem II water-splitting activity in this experiment.
(ii) Identify the treatment that serves as a negative control to demonstrate that light energy is required for photosynthetic electron transport and ATP synthesis.
(c)
(i) Using the data in Table 1, calculate the percent decrease in the rate of ATP synthesis when isolated thylakoids are treated with \(5\ \mu\text{M}\) A-7 compared to the untreated control (Treatment 1).
(ii) Based on Treatments 3 and 4, state the effect of adding DCPIP to thylakoids exposed to \(20\ \mu\text{M}\) A-7 on the rate of \(\text{O}_2\) evolution.
(iii) Based on the data in Table 1, justify the claim that A-7 inhibits electron flow downstream of Photosystem II (between PSII and PSI) rather than directly inhibiting the oxygen-evolving complex of Photosystem II.
(d)
(i) A researcher introduces an uncoupling reagent, FCCP, to untreated thylakoids in the light. FCCP creates channels in the thylakoid membrane that allow protons (\(\text{H}^+\)) to freely diffuse across the lipid bilayer. Predict the effect of adding FCCP on the rate of ATP synthesis AND on the rate of \(\text{O}_2\) evolution compared to Treatment 1.
(ii) Explain the biological reasoning supporting your prediction regarding ATP synthesis.
Researchers are investigating the mechanism of action of a newly developed agricultural compound, Algicide-7 (A-7), on the photosynthetic electron transport chain of the unicellular green alga Chlorella vulgaris. Intact thylakoids were isolated from C. vulgaris cells and incubated in a buffered solution containing \(\text{ADP}\), inorganic phosphate (\(\text{P}_i\)), and oxidized electron acceptors. Samples were exposed to constant illumination (\(400\ \mu\text{mol photons}\cdot\text{m}^{-2}\cdot\text{s}^{-1}\)) at \(22^\circ\text{C}\) under various conditions. In Treatment 4, the artificial electron acceptor DCPIP was added; DCPIP accepts electrons directly from the primary electron acceptor of Photosystem II (PSII) before they reach the cytochrome \(b_6f\) complex. Rates of oxygen evolution, ATP synthesis, and \(\text{NADPH}\) production were measured and recorded in Table 1.
TABLE 1. RATES OF PHOTOSYNTHETIC ACTIVITY IN ISOLATED THYLAKOIDS UNDER VARYING EXPERIMENTAL TREATMENTS
| Treatment | Experimental Conditions | Rate of \(\text{O}_2\) Evolution (\(\mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) | Rate of ATP Synthesis (\(\mu\text{mol ATP}\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) | Rate of \(\text{NADPH}\) Formation (\(\mu\text{mol NADPH}\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\pm 2\text{SE}_x\)) |
| :--- | :--- | :--- | :--- | :--- |
| 1 | No A-7, \(\text{NADP}^+\) present, Light | \(142 \pm 6\) | \(280 \pm 12\) | \(138 \pm 5\) |
| 2 | \(5\ \mu\text{M}\) A-7, \(\text{NADP}^+\) present, Light | \(71 \pm 4\) | \(140 \pm 8\) | \(69 \pm 4\) |
| 3 | \(20\ \mu\text{M}\) A-7, \(\text{NADP}^+\) present, Light | \(8 \pm 2\) | \(15 \pm 3\) | \(7 \pm 2\) |
| 4 | \(20\ \mu\text{M}\) A-7 + DCPIP, No \(\text{NADP}^+\), Light | \(140 \pm 7\) | \(22 \pm 4\) | \(0 \pm 0\) |
| 5 | No A-7, \(\text{NADP}^+\) present, Dark | \(0 \pm 0\) | \(0 \pm 0\) | \(0 \pm 0\) |
(a)
(i) Describe the biological function of water (\(\text{H}_2\text{O}\)) photolysis in the thylakoid lumen during the light-dependent reactions of photosynthesis.
(ii) Explain how the transfer of electrons along the photosynthetic electron transport chain establishes a proton concentration gradient across the thylakoid membrane.
(b)
(i) Identify the dependent variable measured to assess Photosystem II water-splitting activity in this experiment.
(ii) Identify the treatment that serves as a negative control to demonstrate that light energy is required for photosynthetic electron transport and ATP synthesis.
(c)
(i) Using the data in Table 1, calculate the percent decrease in the rate of ATP synthesis when isolated thylakoids are treated with \(5\ \mu\text{M}\) A-7 compared to the untreated control (Treatment 1).
(ii) Based on Treatments 3 and 4, state the effect of adding DCPIP to thylakoids exposed to \(20\ \mu\text{M}\) A-7 on the rate of \(\text{O}_2\) evolution.
(iii) Based on the data in Table 1, justify the claim that A-7 inhibits electron flow downstream of Photosystem II (between PSII and PSI) rather than directly inhibiting the oxygen-evolving complex of Photosystem II.
(d)
(i) A researcher introduces an uncoupling reagent, FCCP, to untreated thylakoids in the light. FCCP creates channels in the thylakoid membrane that allow protons (\(\text{H}^+\)) to freely diffuse across the lipid bilayer. Predict the effect of adding FCCP on the rate of ATP synthesis AND on the rate of \(\text{O}_2\) evolution compared to Treatment 1.
(ii) Explain the biological reasoning supporting your prediction regarding ATP synthesis.
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解题
(a)(i)
* Photolysis of \(\text{H}_2\text{O}\) splits water into electrons (\(e^-\)), protons (\(\text{H}^+\)), and molecular oxygen (\(\text{O}_2\)).
* The biological function is to supply replacement electrons to the oxidized reaction center chlorophyll \(a\) (\(\text{P680}^+\)) in Photosystem II, enabling continuous light absorption and electron flow.
(a)(ii)
* High-energy electrons moving through the electron transport chain (specifically via plastoquinone and the cytochrome \(b_6f\) complex) release free energy, which is used to actively pump protons (\(\text{H}^+\)) from the stroma across the thylakoid membrane into the thylakoid lumen.
* Combined with the release of protons from water photolysis in the lumen and the consumption of protons in the stroma during \(\text{NADP}^+\) reduction, a steep transmembrane electrochemical/proton gradient (lower pH in lumen, higher pH in stroma) is generated.
(b)(i)
* Dependent variable: Rate of \(\text{O}_2\) evolution / production (\(\mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)).
(b)(ii)
* Treatment 5 (no A-7, \(\text{NADP}^+\) present, dark condition).
(c)(i)
* Calculation of percent decrease:
$$\text{Percent decrease} = \frac{\text{Initial Value} - \text{New Value}}{\text{Initial Value}} \times 100\%$$
$$\text{Percent decrease} = \frac{280 - 140}{280} \times 100\% = \frac{140}{280} \times 100\% = 50\%$$ (or \(50.0\%\)).
(c)(ii)
* The addition of DCPIP increases / restores the rate of \(\text{O}_2\) evolution from \(8 \pm 2\) to \(140 \pm 7\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\) (a rate statistically indistinguishable from untreated controls).
(c)(iii)
* In Treatment 3, \(20\ \mu\text{M}\) A-7 drastically reduces \(\text{O}_2\) evolution because the entire electron transport chain becomes back-logged/blocked.
* However, in Treatment 4, when DCPIP is added to accept electrons directly from PSII, \(\text{O}_2\) evolution is completely restored to control levels (\(140\) vs \(142\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)). This confirms that the oxygen-evolving complex and PSII reaction center are intact and functional, proving that A-7 blocks electron transport downstream of PSII (e.g., at the plastoquinone-binding site or cytochrome \(b_6f\) complex).
(d)(i)
* Prediction for ATP synthesis: The rate of ATP synthesis will decrease / drop to near zero.
* Prediction for \(\text{O}_2\) evolution: The rate of \(\text{O}_2\) evolution will remain unchanged or increase (due to relief of photosynthetic control).
(d)(ii)
* ATP synthase requires a proton-motive force (electrochemical gradient of \(\text{H}^+\)) across the thylakoid membrane to catalyze the phosphorylation of \(\text{ADP} + \text{P}_i \rightarrow \text{ATP}\).
* FCCP increases membrane permeability to \(\text{H}^+\), allowing protons to freely diffuse back into the stroma without passing through ATP synthase, thereby dissipating the gradient needed to drive ATP synthesis.
* Photolysis of \(\text{H}_2\text{O}\) splits water into electrons (\(e^-\)), protons (\(\text{H}^+\)), and molecular oxygen (\(\text{O}_2\)).
* The biological function is to supply replacement electrons to the oxidized reaction center chlorophyll \(a\) (\(\text{P680}^+\)) in Photosystem II, enabling continuous light absorption and electron flow.
(a)(ii)
* High-energy electrons moving through the electron transport chain (specifically via plastoquinone and the cytochrome \(b_6f\) complex) release free energy, which is used to actively pump protons (\(\text{H}^+\)) from the stroma across the thylakoid membrane into the thylakoid lumen.
* Combined with the release of protons from water photolysis in the lumen and the consumption of protons in the stroma during \(\text{NADP}^+\) reduction, a steep transmembrane electrochemical/proton gradient (lower pH in lumen, higher pH in stroma) is generated.
(b)(i)
* Dependent variable: Rate of \(\text{O}_2\) evolution / production (\(\mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)).
(b)(ii)
* Treatment 5 (no A-7, \(\text{NADP}^+\) present, dark condition).
(c)(i)
* Calculation of percent decrease:
$$\text{Percent decrease} = \frac{\text{Initial Value} - \text{New Value}}{\text{Initial Value}} \times 100\%$$
$$\text{Percent decrease} = \frac{280 - 140}{280} \times 100\% = \frac{140}{280} \times 100\% = 50\%$$ (or \(50.0\%\)).
(c)(ii)
* The addition of DCPIP increases / restores the rate of \(\text{O}_2\) evolution from \(8 \pm 2\) to \(140 \pm 7\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\) (a rate statistically indistinguishable from untreated controls).
(c)(iii)
* In Treatment 3, \(20\ \mu\text{M}\) A-7 drastically reduces \(\text{O}_2\) evolution because the entire electron transport chain becomes back-logged/blocked.
* However, in Treatment 4, when DCPIP is added to accept electrons directly from PSII, \(\text{O}_2\) evolution is completely restored to control levels (\(140\) vs \(142\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)). This confirms that the oxygen-evolving complex and PSII reaction center are intact and functional, proving that A-7 blocks electron transport downstream of PSII (e.g., at the plastoquinone-binding site or cytochrome \(b_6f\) complex).
(d)(i)
* Prediction for ATP synthesis: The rate of ATP synthesis will decrease / drop to near zero.
* Prediction for \(\text{O}_2\) evolution: The rate of \(\text{O}_2\) evolution will remain unchanged or increase (due to relief of photosynthetic control).
(d)(ii)
* ATP synthase requires a proton-motive force (electrochemical gradient of \(\text{H}^+\)) across the thylakoid membrane to catalyze the phosphorylation of \(\text{ADP} + \text{P}_i \rightarrow \text{ATP}\).
* FCCP increases membrane permeability to \(\text{H}^+\), allowing protons to freely diffuse back into the stroma without passing through ATP synthase, thereby dissipating the gradient needed to drive ATP synthesis.
评分标准
Part (a): 2 points maximum
* (a)(i) Description (1 point):
* Accept one of the following:
* Replaces electrons lost/donated by the reaction center chlorophyll (P680) of Photosystem II.
* Supplies electrons to Photosystem II and releases protons (\(\text{H}^+\)) into the lumen / releases oxygen (\(\text{O}_2\)) as a byproduct.
* (a)(ii) Explanation (1 point):
* Accept one of the following:
* Exergonic/redox reactions along the electron transport chain provide energy to pump protons (\(\text{H}^+\)) from the stroma into the thylakoid lumen.
* Proton accumulation in the thylakoid lumen generated by active proton pumping (cytochrome \(b_6f\) / plastoquinone) and lumenal water oxidation creates a higher concentration of \(\text{H}^+\) inside the lumen relative to the stroma.
Part (b): 2 points maximum
* (b)(i) Identification (1 point):
* Rate of oxygen (\(\text{O}_2\)) evolution/production.
* (b)(ii) Identification (1 point):
* Treatment 5 / the thylakoids incubated in the dark (with \(\text{NADP}^+\) and no A-7).
Part (c): 3 points maximum
* (c)(i) Calculation (1 point):
* \(50\%\) (or \(50\), \(0.50\); setup: \(\frac{280 - 140}{280} \times 100\)).
* (c)(ii) State (1 point):
* DCPIP increases / restores the rate of \(\text{O}_2\) evolution (from \(8\) to \(140\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)).
* (c)(iii) Justification (1 point):
* Accept one of the following:
* In Treatment 4, providing an electron acceptor (DCPIP) directly after PSII completely restores \(\text{O}_2\) production to control levels, indicating that PSII/water photolysis is fully functional and the block is downstream of PSII.
* If A-7 directly inhibited PSII/water splitting, adding an electron acceptor downstream of PSII (DCPIP) would not restore \(\text{O}_2\) evolution.
Part (d): 2 points maximum
* (d)(i) Prediction (1 point):
* ATP synthesis will decrease / cease AND \(\text{O}_2\) evolution will remain unchanged / increase / persist.
(Both predictions required for the 1 point.)
* (d)(ii) Explanation (1 point):
* Accept one of the following:
* FCCP dissipates/eliminates the proton (\(\text{H}^+\)) gradient (proton-motive force), which is required to drive rotation/catalytic activity of ATP synthase.
* Protons leak across the membrane instead of flowing through ATP synthase, preventing phosphorylation of ADP.
* (a)(i) Description (1 point):
* Accept one of the following:
* Replaces electrons lost/donated by the reaction center chlorophyll (P680) of Photosystem II.
* Supplies electrons to Photosystem II and releases protons (\(\text{H}^+\)) into the lumen / releases oxygen (\(\text{O}_2\)) as a byproduct.
* (a)(ii) Explanation (1 point):
* Accept one of the following:
* Exergonic/redox reactions along the electron transport chain provide energy to pump protons (\(\text{H}^+\)) from the stroma into the thylakoid lumen.
* Proton accumulation in the thylakoid lumen generated by active proton pumping (cytochrome \(b_6f\) / plastoquinone) and lumenal water oxidation creates a higher concentration of \(\text{H}^+\) inside the lumen relative to the stroma.
Part (b): 2 points maximum
* (b)(i) Identification (1 point):
* Rate of oxygen (\(\text{O}_2\)) evolution/production.
* (b)(ii) Identification (1 point):
* Treatment 5 / the thylakoids incubated in the dark (with \(\text{NADP}^+\) and no A-7).
Part (c): 3 points maximum
* (c)(i) Calculation (1 point):
* \(50\%\) (or \(50\), \(0.50\); setup: \(\frac{280 - 140}{280} \times 100\)).
* (c)(ii) State (1 point):
* DCPIP increases / restores the rate of \(\text{O}_2\) evolution (from \(8\) to \(140\ \mu\text{mol}\ \text{O}_2\cdot\text{mg Chl}^{-1}\cdot\text{hr}^{-1}\)).
* (c)(iii) Justification (1 point):
* Accept one of the following:
* In Treatment 4, providing an electron acceptor (DCPIP) directly after PSII completely restores \(\text{O}_2\) production to control levels, indicating that PSII/water photolysis is fully functional and the block is downstream of PSII.
* If A-7 directly inhibited PSII/water splitting, adding an electron acceptor downstream of PSII (DCPIP) would not restore \(\text{O}_2\) evolution.
Part (d): 2 points maximum
* (d)(i) Prediction (1 point):
* ATP synthesis will decrease / cease AND \(\text{O}_2\) evolution will remain unchanged / increase / persist.
(Both predictions required for the 1 point.)
* (d)(ii) Explanation (1 point):
* Accept one of the following:
* FCCP dissipates/eliminates the proton (\(\text{H}^+\)) gradient (proton-motive force), which is required to drive rotation/catalytic activity of ATP synthase.
* Protons leak across the membrane instead of flowing through ATP synthase, preventing phosphorylation of ADP.