These are major source of energy for living organisms.
Supplying a huge array of metabolic intermediates for biosynthetic reactions.
The structural elements in cell coat or connective tissues.
The citric acid cycle, also known as the tricarboxylic acid cycle (TCA cycle) or the Krebs cycle—is a series of chemical reactions used by all aerobic organisms to generate energy through the oxidation of acetate—derived from carbohydrates, fats, and proteins—into carbon dioxide.
These are major source of energy for living organisms.
Supplying a huge array of metabolic intermediates for biosynthetic reactions.
The structural elements in cell coat or connective tissues.
The citric acid cycle, also known as the tricarboxylic acid cycle (TCA cycle) or the Krebs cycle—is a series of chemical reactions used by all aerobic organisms to generate energy through the oxidation of acetate—derived from carbohydrates, fats, and proteins—into carbon dioxide.
This file include these contents:
What is Triacylglycerol
Structure of triacylglycerol
Simple triacylglycerol
Mixed triacylglycerol
Biosynthesis of triacylglycerol
Utilization of triacylglycerol
Properties of triacylglycerol
Subject : Nutrition, Unit- VI
This topic provides brief knowledge about lipid metabolism and it is prepared according to INC syllabus for first year BSc Nursing Students.
Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+. The free energy released in this process is used to form the high-energy molecules ATP (adenosine triphosphate) and NADH (reduced nicotinamide adenine ...
Cellular Energy Transfer (Glycolysis and Krebs Cycle) and ATPmuhammad aleem ijaz
This presentation is all about Cellular Energy Transfer with reference to Glycolysis and Kreb Cycle with all their stages involved.
It also includes ATP production in the body, its importance, structure.
Also contains a comparison of energy production in Krebs and Glycolysis cycle.
This file include these contents:
What is Triacylglycerol
Structure of triacylglycerol
Simple triacylglycerol
Mixed triacylglycerol
Biosynthesis of triacylglycerol
Utilization of triacylglycerol
Properties of triacylglycerol
Subject : Nutrition, Unit- VI
This topic provides brief knowledge about lipid metabolism and it is prepared according to INC syllabus for first year BSc Nursing Students.
Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+. The free energy released in this process is used to form the high-energy molecules ATP (adenosine triphosphate) and NADH (reduced nicotinamide adenine ...
Cellular Energy Transfer (Glycolysis and Krebs Cycle) and ATPmuhammad aleem ijaz
This presentation is all about Cellular Energy Transfer with reference to Glycolysis and Kreb Cycle with all their stages involved.
It also includes ATP production in the body, its importance, structure.
Also contains a comparison of energy production in Krebs and Glycolysis cycle.
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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2. Metabolism
• Metabolism is the term refers to all chemical reactions
that occur in the living cells catalyzed by enzymes,
coenzymes, cofactors & regulated by hormones,
vitamins
Aim
• Release energy from ingested food
• Transformation of small organic compound into
macromolecule
4. Anabolism
Involves in the
• biosynthesis of larger and
more complex molecules
• from smaller precursors &
• requires expenditure of
energy
either in the form of
ATP or
using reducing
equivalents storing
NADH/ NADPH
Involves in the
• breakdown of larger molecules
like glucose, amino acid, FA &
• form CO₂, H₂O, NH₃ & energy.
• commonly involving oxidative
reactions;
• they are exothermic, producing
reducing equivalents and
ATP(mainly via the respiratory
chain).
Catabolism
5. Amphibolic pathway
• occur at the ‘crossroads’ of metabolism, acting as links
between the anabolic and catabolic pathways
• can be either anabolic or catabolic, depending on the
energy conditions in the cell
7. Bioenergetics
• Study of energy changes associated with biochemical reaction.
• Free energy [G]: Energy available to do work.
• Standard free energy change [∆G⁰]
• Exergonic/energy yielding reaction
• catabolism
• reaction proceed spontaneously with loss of free energy [∆G
negative]
• Endergonic/energy requiring reaction
• reaction proceed only if free energy is gained [∆G negative]
• Coupled with exergonic reaction
8. Transfer of energy
• Biological system use chemical energy to maintain
living process
• Free energy is obtained by breakdown of complex
organic molecules
• Much of liberated energy is not used directly by the cell
• But there is a formation of bond between phosphoric
acid residue & certain organic compounds
• Different amount of energy is released on hydrolysis of
the bond
9. ATP
• ATP plays a central role in transfer of free energy
• The standard free energy [∆G⁰] on hydrolysis of terminal
phosphate of ATP is -7.3 kcal/mol
• This value divides the biochemically important phosphates
into 2 groups
1. Low energy phosphates: have G⁰ value smaller than
that of ATP.
2. High energy phosphates: G⁰ value is higher than that of
ATP. It include ATP.
11. ATP: Energy carrier
• ATP is able to act as a donor
of high energy phosphate [~P ]
to form low energy phosphate
compounds
• Likewise, ADP can accept ~P
to form ATP
• Thus ATP/ADP cycle connects
those process that generate
~P to those processes that
utilize ~P
12. Biologic oxidation
• Oxidation [removal of electron or H] of biomolecules
within biologic system
• Oxidation is always accompanied by reduction of an
electron acceptor
• Can take place without participation of molecular
oxygen [dehydrogenation]
14. Redox potential
It is the numerical expression of free energy change during
oxidation-reduction.
It is the tendency of any redox pair to lose or gain electron
[quantitatively expressed as E0 with unit in volt]
More negative RP tendency to lose electron
More positive RP tendency to accept electron
H⁺/H₂ -0.42v
NAD⁺/NADH -0.32v
FMN/FMNH₂ -0.22v
15. Respiratory Chain
• Highly organized chain of enzyme & coenzyme in
mitochondria
• Arranged in order of increasing redox potential
• Collect & transport reducing equivalents (H/electron)
16. Respiratory Chain
• In respiratory chain biomolecule become oxidized &
coenzyme reduced
• Reduced coenzyme then deliver 2H to RC through which H
propagate, sequentially reduce & oxidize every component
of chain
• finally get condensed with molecular oxygen to form H₂O,
and the liberated free energy is trapped as ATP (in the
machinery for oxidative phosphorylation).
18. Component of respiratory chain
Four large protein complexes embedded in inner mitochondrial
membrane
1. Complex I : NADH-Q oxidoreductase
2. Complex III : Q-cytochrome c oxidoreductase
3. Complex IV : cytochrome c oxidase
4. Complex II : Succinate-Q reductase (some substrate use it
instead of complex I)
Other component
• Flavoproteins (I & II)
• Iron-Sulfur proteins /Fe-S (I, II & III)
19. Reaction in Respiratory Chain
Salient feature
• Substrate: Reduced coenzyme
• Product: ATP, H₂O
• Site: All cells with mitochondria
• Compartment: Inner mitochondria
• Nature: Catabolic
22. Inhibitors of RC Site of inhibition
Barbiturates Complex I by blocking the transfer from Fe-S to
Q
Antimycin A
Dimercaprol
Complex III
H₂S
Carbon monoxide
Cyanide
Complex IV & totally arrest respiration
Malonate Competitive inhibitor of complex II
Oligomycin Flow of protons through ATP synthase
Uncouplers:-
2,4-dinitrophenol
Thermogenin
Dissociates oxidation in respiratory chain from
phosphorylation
23. Phosphorylation
• Addition of phosphate group to an acceptor molecule by high/
low energy phosphate bond to capture the energy produced
during catabolism.
• 2 types
Oxidative
phosphorylation [at RC]
At substrate level
24. Oxidative phosphorylation
• Flow of electron through respiratory chain generates ATP by a
process called oxidative phosphorylation.
• Oxidation of reduced coenzyme & phosphorylation of ADP are
coupled
• H+ transport results in an electrochemical gradient
• Proton motive force: energy released by flow of H+ down its
gradient is used for ATP synthesis
• ATP synthase: H+ channel that couples energy from H+ flow
with ATP synthesis
25. • Use of ATP
• Synthetic reaction
• Muscle contraction
• Nerve conduction
• Active transport
26. Phosphorylation at substrate level
• ATP can also be formed in some situation when free
energy is released by a chemical reaction. This is
phosphorylation at substrate level.
• 1,3-DPG 3-DPG
ADP ATP