આ MCQ મોડ્યુલ આના પર આધારિત છે: Balance Sheet Amphibolic Rq
Balance Sheet Amphibolic Rq
આ મૂલ્યાંકન આના પર આધારિત હશે: Balance Sheet Amphibolic Rq
મૂલ્યાંકન બનાવવામાં તેમની સામગ્રી સામેલ કરવા ચિત્રો, PDF અથવા Word દસ્તાવેજ અપલોડ કરો.
The Respiratory Balance Sheet, Amphibolic Pathway and Respiratory Quotient
We now have every reaction in place. This part does three things with them: it adds up the ATP and examines honestly how much that total can be trusted, it shows that the pathway is not the one-way demolition it is usually taken for, and it shows how the ratio of two gases can reveal which substrate a tissue is burning.
12.5 The Respiratory Balance Sheet
It is possible to make calculations of the net gain of ATP for every glucose molecule oxidised — but in reality this can remain only a theoretical exercise. The calculations can be made only on certain assumptions.
• There is a sequential, orderly pathway functioning, with one substrate forming the next, and with glycolysis, TCA cycle and ETS pathway following one after another.
• The NADH synthesised in glycolysis is transferred into the mitochondria and undergoes oxidative phosphorylation.
• None of the intermediates in the pathway are utilised to synthesise any other compound.
• Only glucose is being respired — no other alternative substrates are entering the pathway at any of the intermediary stages.
Why none of those assumptions actually holds
But this kind of assumption is not really valid in a living system. The chapter is explicit about why:
- All pathways work simultaneously and do not take place one after another.
- Substrates enter the pathways and are withdrawn from them as and when necessary.
- ATP is utilised as and when needed.
- Enzymatic rates are controlled by multiple means.
Yet it is useful to do this exercise to appreciate the beauty and efficiency of the living system in extraction and storing of energy. On those assumptions, then: there can be a net gain of 38 ATP molecules during aerobic respiration of one molecule of glucose.
What to do. Make a two-column table. In the left column write each of the four assumptions. In the right column, write one concrete biological situation from this chapter or the previous one that violates it. Then state, in one sentence, whether the real yield would be higher or lower than 38.
| Assumption | What actually happens |
|---|---|
| Orderly, sequential pathway | All pathways work simultaneously; glycolysis, the cycle and the ETS run at once, and enzymatic rates are controlled by multiple means, so no neat queue exists. |
| Glycolytic NADH reaches the mitochondria | That NADH is made in the cytoplasm, while the ETS is on the inner mitochondrial membrane. Getting it across is not free, so its full 3-ATP value is not guaranteed. |
| No intermediate is withdrawn | The opposite is routine — and Section 12.6 is built on it. Acetyl CoA is withdrawn when fatty acids must be synthesised, and Krebs' intermediates are withdrawn for amino acids. Every carbon withdrawn is a carbon not oxidised. |
| Only glucose is respired | Fats and proteins are also respired, entering at PGAL, acetyl CoA or points within the Krebs' cycle — so the cell is never running on glucose alone. |
Answer to the prediction: less than 38. Every violation listed removes something from the tally — carbons diverted to synthesis, coenzymes not fully cashed in, ATP spent on transport. So 38 is a theoretical ceiling, not a measurement. The chapter says as much: this “can remain only a theoretical exercise”, valuable because it lets you appreciate the beauty and efficiency of the living system, not because a cell ever hits the number.
12.6 Amphibolic Pathway
Glucose is the favoured substrate for respiration. All carbohydrates are usually first converted into glucose before they are used for respiration. Other substrates can also be respired, but then they do not enter the respiratory pathway at the first step.
Where each substrate joins the pathway
| Substrate | First broken down to | Enters the respiratory pathway as |
|---|---|---|
| Carbohydrates | Glucose | At the first step of glycolysis |
| Fats | Glycerol and fatty acids | See the two rows below |
| — fatty acids | Degraded to acetyl CoA | Acetyl CoA, entering Krebs' cycle |
| — glycerol | Converted to PGAL | PGAL, joining mid-glycolysis |
| Proteins | Degraded by proteases to amino acids, then deaminated | Depending on structure, at some stage within Krebs' cycle, or as pyruvate or acetyl CoA |
Is respiration really just catabolism?
Since respiration involves breakdown of substrates, the respiratory process has traditionally been considered a catabolic process and the respiratory pathway a catabolic pathway. But is this understanding correct?
There is a useful way to picture this. The respiratory pathway is not a one-way demolition chute but a railway junction. Molecules arrive from many directions to be broken down, and molecules are also pulled off the line half-finished to be built into something else. Acetyl CoA is the busiest platform on that junction — the same compound is the gateway for burning a fat and the starting block for making one.
12.7 Respiratory Quotient
During aerobic respiration, O₂ is consumed and CO₂ is released.
The respiratory quotient depends upon the type of respiratory substrate used during respiration.
Carbohydrates — RQ = 1
When carbohydrates are used as substrate and are completely oxidised, the RQ will be 1, because equal amounts of CO₂ and O₂ are evolved and consumed respectively.
RQ = 6CO2 / 6O2 = 1.0
Fats — RQ less than 1
When fats are used in respiration, the RQ is less than 1. For the fatty acid tripalmitin:
RQ = 102CO2 / 145O2 = 0.7
Proteins — RQ about 0.9
When proteins are respiratory substrates, the ratio would be about 0.9.
| Respiratory substrate | RQ | Reason |
|---|---|---|
| Carbohydrates (completely oxidised) | 1.0 | Equal volumes of CO₂ evolved and O₂ consumed |
| Fats (e.g. tripalmitin) | 0.7 — less than 1 | Hydrogen-rich, oxygen-poor substrate needs much more O₂ per CO₂ released |
| Proteins | about 0.9 | Intermediate composition; enter after deamination at various points |
| Organic acids | Greater than 1 | Already highly oxidised, so little O₂ is needed (not required by NCERT, given for context) |
🎯 Interactive: Substrate, entry point and RQ
Enters the pathway as: Glucose, at the first step of glycolysis
Glucose is the favoured substrate, and all carbohydrates are usually first converted into glucose before being respired. Completely oxidised, it gives RQ = 6CO2/6O2 = 1.0, because equal volumes of CO2 are evolved and O2 consumed.
🎯 Competency-Based Questions
Q1. Identify the main respiratory substrate in each seed. L3 Apply
Q2. How confident can you be in those identifications? L5 Evaluate
Q3. Fill in the blanks: The theoretical net gain from one glucose is ______ ATP. This rests on the assumptions of a ______ pathway, that glycolytic ______ reaches the mitochondria, that no ______ is withdrawn for synthesis, and that only ______ is being respired. L1 Remember
Q4. A cell is actively synthesising fatty acids while also respiring. Explain, using one named intermediate, why this makes the 38 ATP figure unattainable. L4 Analyse
Q5. “Respiration is a catabolic process.” Discuss whether this traditional description should be retained. L5 Evaluate
🧠 Assertion–Reason Questions
For each pair choose: (A) Both A and R are true and R is the correct explanation of A. (B) Both A and R are true but R is not the correct explanation of A. (C) A is true but R is false. (D) A is false but R is true.
Assertion (A): The respiratory pathway is best described as amphibolic.
Reason (R): Intermediates such as acetyl CoA are withdrawn from the pathway for synthesis, as well as entering it for breakdown.
Assertion (A): The RQ of fats is less than 1.
Reason (R): Fats are hydrogen-rich and oxygen-poor, so a large volume of O₂ must be consumed relative to the volume of CO₂ evolved.
Assertion (A): A net gain of 38 ATP per glucose is what a plant cell actually obtains from aerobic respiration.
Reason (R): All pathways work simultaneously, substrates are withdrawn as needed, and enzymatic rates are controlled by multiple means.