7. GLYCOSIS:-
• The sequential breakdown
of glucose into pyruvic acid.
• C6H12O6 + 2NAD + 2ADP
+2Pi → 2 CH3COCOOH
+2NADH2 + 2ATP
• Two NADP and two ATP are
the net gain of energy.
8. SITE OF GLYCOLYSIS:-
Cytosol of cytoplasm
TYPES OF GLYCOLYSIS:-
Aerobic glycolysis
Glucose fermentation→ Intermediate
(pyruvate) respiration (O2) → CO2 +H2O
Anaerobic glycolysis
Glucose fermentation→ fermentation product
(lactic acid /Ethyl alcohol)
19. GLYCOLYSIS CYCLE :-
Main steps
PREPARATORY PHASE:-
Glucose activation phase with 1,2,3,4,5 steps
of glycolysis where ATP is utilized.
PAYOFF PHASE:-
Energy extraction phase with the formation
of coupled ATP including last four steps of glycolysis.
33. REACTION IN CYTOSOL
IX. PHOSPHOENOL PYRUVIC ACID:-
It moves into cytosol.
By reverse glycolysis, fructose and glucose
phosphates are formed.
X. Sucrose:-
Finally, sucrose is formed.
34. DIFFERENCE BETWEEN TCA AND GLOXALATE
CYLE:-
TCA CYCLE
•Isocitrate is converted
into glyoxylate and
succinate by alpha
ketoglutarate.
•It uses eight enzymes
GYLOXALTAE CYLCLE
•Isocitrate is converted
into glyoxylate and
succinate by ICL.
•It uses five enzymes.
35. Significance of glyoxylate pathway :
i. It is gluconeogenesis reaction.
ii. Bypass of TCA cycle.
iii. In nematodes, on early stage of emryogenesis.
iv. In bacteria, cultured in acetate rich carbon source
37. TRICARBOXYLIC
ACID CYCLE (TCA):-
A series of enzyme
catalyzed reaction used
by all aerobic organism to
release stored energy
through the oxidation of
acetyl Co-A.
39. DISCOVERY:-
INITIATION
• Discovered in 1930 by
Albert Szent Gyorgyi.
FINAL IDENTIFICATION:-
• finally identified in 1937 by
Hans Adolf Krebs and William
Arthur Johnson.
EVOLUTION:-
Evolved from anaerobic bacteria.
Initiator is acetyl-CoA.
40. STEPS OF CITRIC ACID OR TCA CYCLE:-
• Irreversible, extends the 4C oxaloacetate to a 6C molecule.
• Reversible isomerization.
• Generates NADH (equivalent of 2.5 ATP).
• Rate-limiting, irreversible stage, generates a 5C molecul.e
• Irreversible stage, generates NADH.
• Condensation reaction of GDP+ Pi and hydrolysis of Succinyl-CoA.
• Uses FAD as a prosthetic group (FAD→FADH2 in the first step of the
reaction).
• Hydration of C-C double bond.
• Reversible (in fact, equilibrium favors malate), generates NADH.