Level 5 — MasteryPhotosynthesis

Photosynthesis

75 minutes60 marksprintable — key stays hidden on paper

Time limit: 75 minutes
Total marks: 60
Instructions: Answer ALL questions. Show all working, including units and any assumptions. Calculators and pseudocode are permitted where indicated.


Question 1 — Energetics, Stoichiometry & the Overall Equation (20 marks)

The overall equation for photosynthesis can be written as:

6CO2+12H2OlightC6H12O6+6O2+6H2O6\,CO_2 + 12\,H_2O \xrightarrow{\text{light}} C_6H_{12}O_6 + 6\,O_2 + 6\,H_2O

(a) Explain why the equation is written with 12 water molecules on the left and 6 regenerated on the right, rather than the simplified 6 CO₂ + 6 H₂O. Link your answer explicitly to photolysis and the fate of oxygen atoms. (4 marks)

(b) The standard Gibbs free energy change for synthesising one mole of glucose is ΔG=+2870 kJ mol1\Delta G^{\circ} = +2870\ \text{kJ mol}^{-1}. A photon of red light at wavelength λ=680 nm\lambda = 680\ \text{nm} carries energy E=hc/λE = hc/\lambda, with h=6.626×1034 J sh = 6.626\times10^{-34}\ \text{J s} and c=3.00×108 m s1c = 3.00\times10^{8}\ \text{m s}^{-1}.

(i) Calculate the energy of one mole of 680 nm photons (use Avogadro's number NA=6.022×1023N_A = 6.022\times10^{23}). (3 marks)

(ii) The non-cyclic light-dependent reactions require the absorption of a minimum of 8 photons per O₂ molecule released (through Photosystems I and II). Determine the minimum number of moles of 680 nm photons required to make one mole of glucose, and hence the minimum light energy input. (3 marks)

(iii) Compute the maximum theoretical efficiency η=ΔG/Ephotons\eta = \Delta G^{\circ} / E_{\text{photons}} as a percentage. Comment on why real leaf efficiency (~1–2%) is far lower. (3 marks)

(c) Photosynthesis and aerobic respiration are often described as "opposite" processes. Construct a comparison identifying two similarities and four differences (organelle, energy flow, redox direction, and net ATP), and explain why they are NOT exact chemical reverses despite similar overall equations. (4 marks)


Question 2 — Modelling Light-Dependent Reactions & Photophosphorylation (22 marks)

(a) Draw (or describe in a labelled linear diagram) the Z-scheme of non-cyclic electron flow, naming: PSII, the plastoquinone/cytochrome b6f/plastocyanin chain, PSI, ferredoxin, and NADP⁺ reductase. State at which point(s) the electron gains energy and where ATP is generated. (5 marks)

(b) Non-cyclic photophosphorylation produces both ATP and NADPH; cyclic photophosphorylation produces only ATP. The Calvin cycle consumes ATP and NADPH in the ratio 3 ATP : 2 NADPH per CO₂ fixed.

(i) Assume non-cyclic flow produces ATP and NADPH in a fixed ratio of 3 ATP : 2 NADPH per 2 CO₂ (i.e. per O₂). Show whether non-cyclic flow alone exactly balances the Calvin cycle demand, per CO₂. (3 marks)

(ii) Suppose instead the measured non-cyclic ratio is only 2.6 ATP : 2 NADPH per O₂. Write a short algorithm (pseudocode) that, given the Calvin demand 3 ATP : 2 NADPH per CO₂ and the non-cyclic output, computes the extra ATP per CO₂ that must be supplied by cyclic photophosphorylation. Then evaluate it numerically. (4 marks)

(c) Explain the chemiosmotic mechanism: how does the proton gradient across the thylakoid membrane arise (name three proton sources/pumps), and how is it coupled to ATP synthesis? (5 marks)

(d) A researcher adds a chemical that makes the thylakoid membrane freely permeable to H⁺ (an uncoupler). Predict, with reasoning, the effect on: (i) the proton gradient, (ii) ATP synthesis, (iii) electron transport rate, and (iv) O₂ evolution. (5 marks)


Question 3 — RuBisCO, C3/C4/CAM & Photorespiration under Limiting Factors (18 marks)

(a) RuBisCO catalyses both carboxylation (with CO₂) and oxygenation (with O₂) of RuBP.

(i) Write the two competing reactions (products only need be named). Explain why rising temperature and low CO₂:O₂ ratio favour the oxygenase (photorespiration) pathway. (4 marks)

(ii) Explain the carbon and energy cost of photorespiration to a C3 plant. (3 marks)

(b) C4 and CAM plants both concentrate CO₂ around RuBisCO but separate the steps differently.

Construct a comparison table distinguishing C3, C4, and CAM on: initial CO₂ acceptor & first fixed product, enzyme of primary fixation, spatial/temporal separation, and typical habitat. (6 marks)

(c) In an experiment, net photosynthetic rate is measured as CO₂ concentration increases at two light intensities (low and high). Sketch/describe the two expected curves and use the concept of limiting factors to explain: (i) why both curves plateau, (ii) why the high-light curve plateaus at a higher rate, and (iii) identify what is limiting in each region of the low-light curve. (5 marks)


Answer keyMark scheme & solutions

Question 1 (20 marks)

(a) (4 marks)

  • 12 H₂O on the left because photolysis splits water to supply electrons/protons and release O₂ (1). Each O₂ requires 2 H₂O split → 6 O₂ needs 12 H₂O (1).
  • Isotope labelling (⁠¹⁸O) shows the O₂ released comes entirely from water, not CO₂ (1).
  • 6 H₂O reappear on the right because they are regenerated during the Calvin cycle / condensation reactions (e.g. ATP hydrolysis, sugar formation) (1). Net water consumed = 6.

(b)(i) (3 marks) Ephoton=hc/λ=(6.626×1034)(3.00×108)680×109E_{\text{photon}} = hc/\lambda = \dfrac{(6.626\times10^{-34})(3.00\times10^{8})}{680\times10^{-9}} =2.923×1019 J= 2.923\times10^{-19}\ \text{J} (1) Per mole: E=2.923×1019×6.022×1023=1.760×105 J=176.0 kJ mol1E = 2.923\times10^{-19}\times6.022\times10^{23} = 1.760\times10^{5}\ \text{J} = 176.0\ \text{kJ mol}^{-1} (2).

(b)(ii) (3 marks)

  • 8 photons per O₂; 6 O₂ per glucose → 8×6=488\times6 = 48 mol photons per mol glucose (1).
  • Energy = 48×176.0=8448 kJ48 \times 176.0 = 8448\ \text{kJ} (≈ 8.45×1038.45\times10^{3} kJ) (2).

(b)(iii) (3 marks) η=28708448=0.3397=34.0%\eta = \dfrac{2870}{8448} = 0.3397 = 34.0\% (2). Real efficiency much lower because: reflection/transmission of light, absorption by non-photosynthetic pigments, photorespiration, saturation/limiting factors, respiratory losses, and only certain wavelengths are usable (1, any valid reason).

(c) (4 marks)

  • Similarities (any 2, 1 mark total): both are redox reactions involving electron transport chains and chemiosmotic ATP synthesis; both use similar electron carriers (NADP⁺/NAD⁺) and membrane-bound ATP synthase.
  • Differences (2 marks, ½ each):
    • Organelle: chloroplast vs mitochondrion.
    • Energy flow: photosynthesis stores light energy (endergonic, +ΔG) vs respiration releases energy (exergonic, −ΔG).
    • Redox: photosynthesis reduces CO₂ to sugar (reduction/anabolic); respiration oxidises sugar to CO₂ (oxidation/catabolic).
    • Net ATP: respiration yields net ATP; light reactions produce ATP but Calvin cycle consumes it — net storage is in sugar not ATP.
  • Not exact reverses (1 mark): different intermediates, enzymes, electron carriers (NADPH vs NADH), and pathways; oxygen source differs; energetically the pathways are not simply the reverse mechanism.

Question 2 (22 marks)

(a) (5 marks) Linear Z-scheme (1 mark per correct labelled element, max 5): PSII (P680) → photolysis supplies e⁻ → plastoquinone (PQ) → cytochrome b6f complex (proton pumping/ATP generation here) → plastocyanin (PC) → PSI (P700) → ferredoxin (Fd) → NADP⁺ reductase → NADPH. Electron gains energy at PSII and PSI (light absorption boosts it to higher energy). ATP generated via proton gradient built at the cytochrome b6f step.

(b)(i) (3 marks) Non-cyclic gives 3 ATP : 2 NADPH per O₂; per O₂ = 2 CO₂ fixed, so per CO₂ = 1.5 ATP : 1 NADPH. Calvin demand per CO₂ = 3 ATP : 2 NADPH = 1.5 ATP : 1 NADPH. These are equal ratios → non-cyclic alone exactly matches demand in this idealised case (3). (Award full marks for showing the per-CO₂ scaling and equality.)

(b)(ii) (4 marks) Pseudocode (2 marks):

INPUT demand_ATP = 3, demand_NADPH = 2   # per CO2
INPUT nc_ATP = 2.6, nc_NADPH = 2         # per O2 = per 2 CO2
# scale non-cyclic output to per CO2
nc_ATP_perCO2 = nc_ATP / 2
nc_NADPH_perCO2 = nc_NADPH / 2
extra_ATP = demand_ATP - nc_ATP_perCO2   # NADPH assumed sufficient
OUTPUT extra_ATP

Evaluation (2 marks): nc_ATP_perCO2 = 2.6/2 = 1.3; extra_ATP = 3 − 1.3 = 1.7 ATP per CO₂ must come from cyclic photophosphorylation.

(c) (5 marks)

  • Protons accumulate in the thylakoid lumen creating an electrochemical gradient (1).
  • Three sources (1 each): (i) photolysis of water releases H⁺ into the lumen; (ii) the cytochrome b6f complex pumps H⁺ from stroma into lumen as electrons pass; (iii) reduction of NADP⁺ in the stroma consumes H⁺, lowering stromal [H⁺] and steepening the gradient.
  • Coupling (1): protons flow back through ATP synthase (CF₀CF₁); the energy released drives phosphorylation of ADP + Pi → ATP (chemiosmosis).

(d) (5 marks) (1 mark each, +1 for reasoning quality)

  • (i) Proton gradient collapses/dissipates because H⁺ leaks back freely across the membrane.
  • (ii) ATP synthesis stops/falls — no proton-motive force to drive ATP synthase.
  • (iii) Electron transport rate INCREASES (or stays high) — without a back-pressure gradient, electron flow is no longer restricted ("uncoupled").
  • (iv) O₂ evolution continues (may increase) since photolysis/electron flow proceeds; O₂ production is decoupled from ATP output.

Question 3 (18 marks)

(a)(i) (4 marks)

  • Carboxylation: RuBP + CO₂ → 2 × 3-phosphoglycerate (2×3C) (1).
  • Oxygenation: RuBP + O₂ → 1 × 3-phosphoglycerate + 1 × 2-phosphoglycolate (1).
  • High temperature decreases CO₂ solubility relative to O₂ and reduces RuBisCO's specificity for CO₂; stomatal closure in heat lowers internal CO₂ raising O₂:CO₂ ratio → favours oxygenase (2).

(a)(ii) (3 marks)

  • Photorespiration consumes fixed carbon: 2-phosphoglycolate is salvaged in a pathway (peroxisome/mitochondrion) that releases previously fixed CO₂ (1).
  • It consumes ATP and reducing power (energy cost) without net sugar gain (1).
  • Net effect: reduces photosynthetic efficiency/yield by up to ~25% in C3 plants (1).

(b) (6 marks) — ½ mark per correct cell (12 cells):

Feature C3 C4 CAM
Initial CO₂ acceptor RuBP PEP (phosphoenolpyruvate) PEP
First fixed product 3-PGA (3C) Oxaloacetate (4C) Oxaloacetate → malate (4C)
Primary fixation enzyme RuBisCO PEP carboxylase PEP carboxylase
Separation none spatial (mesophyll vs bundle sheath) temporal (night vs day)
Typical habitat temperate/moist hot, high-light (tropical grasses) arid/desert (succulents)

(c) (5 marks)

  • (i) Both curves plateau because another factor becomes limiting once CO₂ is no longer limiting (light, temperature, or enzyme/RuBisCO saturation) (1).
  • (ii) High-light curve plateaus higher because light is not limiting; the plateau is set by CO₂-independent factors so more CO₂ can be used before saturation, and the light reactions supply more ATP/NADPH (2).
  • (iii) On the low-light curve: at low CO₂ the initial rising region is CO₂-limited (1); at the plateau, light intensity is the limiting factor (1).

[
  {"claim": "One mole of 680nm photons carries ~176 kJ", "code": "h=6.626e-34; c=3.00e8; lam=680e-9; Na=6.022e23; E=h*c/lam*Na/1000; result = abs(E-176.0)<1.0"},
  {"claim": "Minimum photon energy per mole glucose is ~8448 kJ (48 mol photons)", "code": "h=6.626e-34; c=3.00e8; lam=680e-9; Na=6.022e23; Emol=h*c/lam*Na/1000; Etot=48*Emol; result = abs(Etot-8448)<50"},
  {"claim": "Max theoretical efficiency ~34%", "code": "eff=2870/8448*100; result = abs(eff-34.0)<1.0"},
  {"claim": "Extra ATP from cyclic per CO2 is 1.7 when non-cyclic gives 2.6 ATP:2 NADPH per O2", "code": "nc_ATP_perCO2=Rational(26,10)/2; extra=3-nc_ATP_perCO2; result = extra==Rational(17,10)"},
  {"claim": "Non-cyclic 3ATP:2NADPH per O2 equals Calvin demand per CO2", "code": "result = (Rational(3,2)==Rational(3,1)/2) and (Rational(2,2)==Rational(2,1)/2)"}
]