1. Beta-oxidation is the process by which fatty acids are broken down in the mitochondria to generate acetyl-CoA molecules.
2. It occurs in four steps: activation of fatty acids in the cytosol, transport into the mitochondria via carnitine shuttle, and three steps of beta-oxidation in the mitochondrial matrix involving dehydrogenation, hydration, and thiolytic cleavage.
3. This process is repeated, producing acetyl-CoA with each turn, until the fatty acid is completely broken down, yielding large amounts of ATP through the citric acid cycle and oxidative phosphorylation.
This PPT is on Amino acid metabolism. And the topics covered under this ppt are Transamination, deamination
Book referred: https://www.amazon.in/Biochemistry-2019-Satyanarayana-Satyanarayana-Author/dp/B07WGHCTKZ/ref=sr_1_1?dchild=1&qid=1591608419&refinements=p_27%3AU+Satyanarayana&s=books&sr=1-1
Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+.
Gluconeogenesis- Steps, Regulation and clinical significanceNamrata Chhabra
Gluconeogenesis- Thermodynamic barriers, substrates of gluconeogenesis, reciprocal regulation of glycolysis and gluconeogenesis, biological and clinical significance
Complete Set of Metabolism of Carbohydrate in that second chapter, glycolysis.
This presentation covers complete glycolysis pathway with step wise animated reactions and it includes clinical aspects also. This presentation is good for MBBS students.
This PPT is on Amino acid metabolism. And the topics covered under this ppt are Transamination, deamination
Book referred: https://www.amazon.in/Biochemistry-2019-Satyanarayana-Satyanarayana-Author/dp/B07WGHCTKZ/ref=sr_1_1?dchild=1&qid=1591608419&refinements=p_27%3AU+Satyanarayana&s=books&sr=1-1
Glycolysis (from glycose, an older term for glucose + -lysis degradation) is the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO− + H+.
Gluconeogenesis- Steps, Regulation and clinical significanceNamrata Chhabra
Gluconeogenesis- Thermodynamic barriers, substrates of gluconeogenesis, reciprocal regulation of glycolysis and gluconeogenesis, biological and clinical significance
Complete Set of Metabolism of Carbohydrate in that second chapter, glycolysis.
This presentation covers complete glycolysis pathway with step wise animated reactions and it includes clinical aspects also. This presentation is good for MBBS students.
This ppt has been presented as seminar in Department of Biochemistry ,C.C.S. university, Meerut.in front of all faculty members for the detailed discussion on this topic. Hope this will help you to go through the concept in an easy manner.
It is the catabolic process by which fatty acid molecules are broken down in the cytosol in prokaryotes and in the mitochondria in eukaryotes to generate acetyl-CoA.
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Salas, V. (2024) "John of St. Thomas (Poinsot) on the Science of Sacred Theol...Studia Poinsotiana
I Introduction
II Subalternation and Theology
III Theology and Dogmatic Declarations
IV The Mixed Principles of Theology
V Virtual Revelation: The Unity of Theology
VI Theology as a Natural Science
VII Theology’s Certitude
VIII Conclusion
Notes
Bibliography
All the contents are fully attributable to the author, Doctor Victor Salas. Should you wish to get this text republished, get in touch with the author or the editorial committee of the Studia Poinsotiana. Insofar as possible, we will be happy to broker your contact.
Nutraceutical market, scope and growth: Herbal drug technologyLokesh Patil
As consumer awareness of health and wellness rises, the nutraceutical market—which includes goods like functional meals, drinks, and dietary supplements that provide health advantages beyond basic nutrition—is growing significantly. As healthcare expenses rise, the population ages, and people want natural and preventative health solutions more and more, this industry is increasing quickly. Further driving market expansion are product formulation innovations and the use of cutting-edge technology for customized nutrition. With its worldwide reach, the nutraceutical industry is expected to keep growing and provide significant chances for research and investment in a number of categories, including vitamins, minerals, probiotics, and herbal supplements.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
2. Triglycerides
• Fats are called as the Triglycerides which are important source
of energy
• 1gm of fat gives 9 kcal energy
• Mainly as triacylglycerols in adipose cells
• They Constitute 84% of stored energy
• Protein - 15%
• Carbohydrate (glucose or glycogen) - <1%
4. βoxidation of fatty acids
Beta –oxidation is defined as the oxidation and splitting of two
carbon units at beta (second) carbon atom. This results in
sequential removal of 2 carbon fragments as acetyl CoA until the
complete oxidation of fatty acids. Beta oxidation occurs almost in
all tissues except, erythrocytes and adrenal medulla. Beta -
oxidation of fatty acid- The break down of a fatty acid to acetyl-
CoA.
Occurs in the mitochondria
Process is strictly aerobic
After production Acetyl-CoA is fed directly into the Krebs
cycle
It occurs in many tissues including liver, kidney and heart.
Fatty acids oxidation doesn't occur in the brain
5. The beta oxidation of fatty acids involve three
stages:
Activation of fatty acids in the cytosol
Transport of activated fatty acids into
mitochondria (carnitine shuttle)
Beta oxidation proper in the mitochondrial matrix
6. Activation of Fatty Acid:
This proceeds by FattyAcidthiokinase (acyl COA synthetase)
present in cytosol
Thiokinase requires ATP,COA SH, Mg++.The product of this
reaction is FAacyl COA and water.
7. 2- Transport of fatty acyl CoA from cytosol
into mitochondria:
Long chain acyl CoA traverses the inner mitochondria
membrane with a special transport mechanism called
Carnitine shuttle
8. 2-Transport of acyl CoA into the
mitochondria
It is called as the rate limiting step
Acyl groups from acyl COA is transferred to carnitine to form acyl
carnitine catalyzed by carnitine acyltransferase I, in the outer
mitochondrial membrane.
Acylcarnitine is then shuttled across the inner mitochondrial
membrane by a translocase enzyme.
The acyl group is transferred back to CoA in matrix by carnitine acyl
transferase II.
Finally, carnitine is returned to the cytosolic side by translocase, in
exchange for an incoming acyl carnitine
9.
10. β – oxidation in the mitochondrial
matrix
There are 4 steps in β – oxidation
Step I – Oxidation by FAD linked dehydrogenase
Step II – Hydration by Hydratase
Step III – Oxidation by NAD linked dehydrogenase
Step IV – Thiolytic clevage Thiolase
11. Step I – Oxidation by FAD linked dehydrogenase
The first reaction is the oxidation of acyl CoA by an acyl
CoA dehyrogenase to give α-β unsaturarted acyl CoA
(enoyl CoA).
FAD is the hydrogen acceptor.
12. Step II – Hydration by Hydratase
The second reaction is the hydration of the double bond to β-hydroxyacyl CoA (p- hydroxyacyl CoA).
13. Step III – Oxidation by NAD linked dehydrogenase
The third reaction is the oxidation of β- hydroxyacyl CoA to
produce β-Ketoacyl CoA a NAD-dependent reaction.
14. Step IV – Thiolytic clevage Thiolase
• The fourth reaction is cleavage of the two carbon
fragment by splitting the bond between α and β carbons
• By thiolase enzyme.
15.
16.
17. • The release of acetyl CoA leaves an acyl CoA molecule shortened by 2
carbons.
• This acyl CoA molecule is the substrate for the next round of oxidation starting
with acyl CoA dehydrogenase.
• Repetition continues until all the carbons of the original fatty acyl CoA are
converted to acetyl CoA.
• In the last round a four carbon acyl CoA (butyryl CoA) is cleaved to 2
acetyl CoA
18.
19.
20.
21.
22.
23.
24.
25. Examples
1. e.g. Palmitic (16C): β-oxidation of palmitic acid will be
repeated 7 cycles producing 8 molecules of acetyl
COA.
2. In each cycle FADH2 and NADH+H+ is
produced and will be transported to the
respiratory chain.
26. Each acetyl COA which is oxidized in citric cycle gives
12 ATP (8 x 12 = 96 ATP)
2 ATP are utilized in the activation of fatty acid (It occurs
once).
Energy gain = Energy produced - Energy utilized
= 35 ATP + 96 ATP - 2 ATP = 129 ATP