This document summarizes fatty acid oxidation and beta-oxidation. It describes that fatty acid oxidation occurs in the mitochondria to break down fatty acids into acetyl-CoA, generating energy. Beta-oxidation involves four steps - oxidation, hydration, oxidation again, and cleavage - to sequentially remove two-carbon acetyl-CoA units from the fatty acid. The acetyl-CoA can then enter the citric acid cycle to generate more energy through oxidative phosphorylation.
Pentose phosphate pathway is also called Hexose monophosphate pathway/ HMP shunt/ Phosphogluconate pathway.
It is an alternative route for the metabolism of glucose.
It is more complex pathway than glycolysis.
It is more anabolic in nature.
It takesplace in cytosol.
The tissues such as liver, adipose tissue, adrenal gland, erythrocytes,testes and lactating mammary gland are highly active in HMP shunt.
It concern with the biosynthesis of NADPH and pentoses.
De novo synthesis of fatty acids (Biosynthesis of fatty acids)Ashok Katta
Synthesis of fatty acids in the body. Detailed pathway for de novo synthesis of fatty acids in the body including its energetic and regulation. also cover Multienzyme complex
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.
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 ...
Substrate level phosphorylation and it's mechanism || Biochemistry || B Pharmacy || Project || slideshare || biology || chemistry
*images use in this ppt is only for educational purpose
In this presentation, i tell about substrate level phosphorylation
Phosphorylation involves the transfer of phosphate
group from one compound to other.
➢ Substrate level phosphorylation is a direct
phosphorylation of ADP with a phosphatase group by
using the energy obtain from a coupled reaction.
➢ Occurs in cytoplasm ( glycolysis – due to aerobic and
anaerobic condition) and in mitochondrial matrix ( krebs
cycle – anaerobic condition)
Biological oxidation (part - III) Oxidative PhosphorylationAshok Katta
Biological oxidation (part - III) Oxidative Phosphorylation
- Mechanism of Oxidative Phosphorylation
-- Chemiosmotic theory
-P:O Ratio
Substrate Level Phosphorylation
Shuttle Systems for Oxidation of Extramitochondrial NADH
Fatty acid oxidation
Types of fatty acid oxidation
Overview of fatty acid oxidation
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
Stoichiometry of Beta oxidation
Reference
Pentose phosphate pathway is also called Hexose monophosphate pathway/ HMP shunt/ Phosphogluconate pathway.
It is an alternative route for the metabolism of glucose.
It is more complex pathway than glycolysis.
It is more anabolic in nature.
It takesplace in cytosol.
The tissues such as liver, adipose tissue, adrenal gland, erythrocytes,testes and lactating mammary gland are highly active in HMP shunt.
It concern with the biosynthesis of NADPH and pentoses.
De novo synthesis of fatty acids (Biosynthesis of fatty acids)Ashok Katta
Synthesis of fatty acids in the body. Detailed pathway for de novo synthesis of fatty acids in the body including its energetic and regulation. also cover Multienzyme complex
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.
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 ...
Substrate level phosphorylation and it's mechanism || Biochemistry || B Pharmacy || Project || slideshare || biology || chemistry
*images use in this ppt is only for educational purpose
In this presentation, i tell about substrate level phosphorylation
Phosphorylation involves the transfer of phosphate
group from one compound to other.
➢ Substrate level phosphorylation is a direct
phosphorylation of ADP with a phosphatase group by
using the energy obtain from a coupled reaction.
➢ Occurs in cytoplasm ( glycolysis – due to aerobic and
anaerobic condition) and in mitochondrial matrix ( krebs
cycle – anaerobic condition)
Biological oxidation (part - III) Oxidative PhosphorylationAshok Katta
Biological oxidation (part - III) Oxidative Phosphorylation
- Mechanism of Oxidative Phosphorylation
-- Chemiosmotic theory
-P:O Ratio
Substrate Level Phosphorylation
Shuttle Systems for Oxidation of Extramitochondrial NADH
Fatty acid oxidation
Types of fatty acid oxidation
Overview of fatty acid oxidation
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
Stoichiometry of Beta oxidation
Reference
Fatty acid β-oxidation is the process by which fatty acids are broken down to produce energy. Fatty acids primarily enter a cell via fatty acid protein transporters on the cell surface. Once inside, FACS adds a CoA group to the fatty acid. CPT1 then converts the long-chain acyl-CoA to long-chain acylcarnitine.
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.
Beta-Oxidation may be defined as the oxidation of fatty acids on the beta-carbon atom.
This results in the sequential removal of a two carbon fragment, acetyl CoA.
UNDERSTANDING THE INVOLVEMENT OF N-TERMINAL DOMAIN OF FATS IN INTERACTION WIT...Santosh Kumar Sahoo
Fat family members (FAT1, FAT2, FAT3, and FAT4) are human homologs of Drosophila Fat and are implicated in tumour suppression and planar cell polarity. Cellular homeostasis is largely maintained at the cellular level via transcription regulation, which can vary in response to physiological alterations. FAT atypical cadherin 1 (FAT1), which encodes a protocadherin, is one of the most frequently mutated genes in human cancer. FAT1 is thought to play a vital role in the maintenance of organ and cellular homeostasis, as well as activating a number of signalling pathways via protein-protein interactions, such as the Wnt/catenin, Hippo, and MAPK/ERK signaling pathways. Unregulated FAT1 expression can cause cancer and have a negative impact on prognosis. In this study, we focused on the structural and functional aspects of various domains and motifs of FAT1. Global bioinformatic databases resulted in streamlining a list of putative protein associates of FAT1. Since FAT1-mediated structural and functional alterations, as well as variations in FAT1 expression, contribute to disturbances in cellular homeostasis and result in patho-physiological disorders including cancer, we essentially focused on cancer-related genes functionally related to the FAT1. FAT1 is a huge protein composed of 4588 amino acid residues. By mutational analysis and further protein-protein docking studies using multiple bioinformatic tools it was confirmed that the C-terminus 4204-4214 and 4300-4400 amino acid residues are critical for interaction with cancer-related genes including Tumor necrosis factor, Myc proto-oncogene and Rela proto-oncogene. Interestingly, it was found that the small peptides corresponding to the C-terminus domain 4204-4214 and 4300-4400 of FAT1 effectively interact with tumor-suppressor genes. These evidences widens up the possibility of administering potential peptides when the FAT1 expression is inhibited. Our preliminary results will pave way forward in improving the prognosis and treatment of patients with cancer.
Polymerase Chain Reaction
History of PCR
Instrumentation of PCR
Principle of PCR
Components of PCR
Steps of PCR
Optimal PCR Factors
Applications of PCR
Introduction
Fish Health Management GOALS
Principles of fish health management
Factors affecting fish health
Common symptoms of diseases
General preventive measures
Proper Health Management through manipulating the disease triangle
Conclusion
References
NCBI; Introduction, Homepage and about
Tools and database of NCBI
BLAST; Introduction, Homepage and types of BLAST
Some databases of NCBI
References
Acknowledgements
vector born diseases
malaria facts
Malaria; One of the world’s deadliest vectorborne diseases
Global malaria scenario; As for World
Malaria report 2020
Current Malaria scenario in INDIA
malaria vector control
prevention
Introduction
Fish Health Management GOALS
Principles of fish health management
Factors affecting fish health
Common symptoms of diseases
General preventive measures
Proper Health Management through Manipulating the disease triangle
Conclusion
References
Palestine last event orientationfvgnh .pptxRaedMohamed3
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Model Attribute Check Company Auto PropertyCeline George
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Bills have a main role in point of sale procedure. It will help to track sales, handling payments and giving receipts to customers. Bill splitting also has an important role in POS. For example, If some friends come together for dinner and if they want to divide the bill then it is possible by POS bill splitting. This slide will show how to split bills in odoo 17 POS.
Ethnobotany and Ethnopharmacology:
Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
New development in herbals,
Bio-prospecting tools for drug discovery,
Role of Ethnopharmacology in drug evaluation,
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This is a presentation by Dada Robert in a Your Skill Boost masterclass organised by the Excellence Foundation for South Sudan (EFSS) on Saturday, the 25th and Sunday, the 26th of May 2024.
He discussed the concept of quality improvement, emphasizing its applicability to various aspects of life, including personal, project, and program improvements. He defined quality as doing the right thing at the right time in the right way to achieve the best possible results and discussed the concept of the "gap" between what we know and what we do, and how this gap represents the areas we need to improve. He explained the scientific approach to quality improvement, which involves systematic performance analysis, testing and learning, and implementing change ideas. He also highlighted the importance of client focus and a team approach to quality improvement.
We all have good and bad thoughts from time to time and situation to situation. We are bombarded daily with spiraling thoughts(both negative and positive) creating all-consuming feel , making us difficult to manage with associated suffering. Good thoughts are like our Mob Signal (Positive thought) amidst noise(negative thought) in the atmosphere. Negative thoughts like noise outweigh positive thoughts. These thoughts often create unwanted confusion, trouble, stress and frustration in our mind as well as chaos in our physical world. Negative thoughts are also known as “distorted thinking”.
Instructions for Submissions thorugh G- Classroom.pptxJheel Barad
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2. CONTENTS
Fatty acid oxidation
Types of fatty acid oxidation
Overview of fatty acid oxidation
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
Stoichiometry of Beta oxidation
Reference
3. Fatty acid oxidation
Fatty acid contains a long hydrocarbon chain anda terminal carboxylate group.
The hydrocarbonchain may be saturated (with no double bond) or may be
unsaturated (containing double bond).
Fatty acid Oxidation is the process where energy is produced by degradation of
fatty acids.
• Major mechanism, occurs in themitochondria matrix.
• 2-C units are released asacetyl CoA per cycle
Beta oxidation
• Predominantly takes place inbrain and liver,
• one carbon is lost in the form ofCO2 per cycle
Alpha
oxidation
• Minor mechanism, but becomes important in
conditions of impaired beta oxidation
Omega
oxidation
Types of fatty acid oxidation
4. Stage 1:
A long-chain fatty acid is
oxidized to yield acetyl
residues in the form of acetyl-
CoA. This process is called
Beta oxidation.
Stage 2:
The acetyl groups are
oxidized to CO2 via the
citric acid cycle.
Stage 3:
Electrons derived from the oxidations
of stages 1 and 2 pass to O2 via the
mitochondrial respiratory chain,
providing the energy for ATP synthesis
by oxidative phosphorylation.
Overview of fatty acid oxidation
5. Beta-Oxidation may be defined as the oxidation of fatty acids on the beta-
carbon atom.
This results in the sequential removal of a two carbon fragment, acetyl CoA.
Occurs in the mitochondria and 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.
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
7. The inner mitochondrial membrane is impermeable to fatty acids.
A specialized carnitine carrier system (carnitine shuttle) operates to transport
activated fatty acids from cytosol to the mitochondria.
This occurs in four steps
1. Acyl group of acyl CoA is transferred to carnitine (β-hydroxy γ-trimethyl
aminobutyrate) catalyzed by carnitine acyltransferasIe (CAT) (present on the outer
surface of inner mitochondrial membrane).
2. The acyl-carnitine is transported across the membrane to mitochondrial matrix by a
specific carrier protein.
3. Carnitine acyl transferase ll (found on the inner surface of inner mitochondrial
membrane) converts acyl-carnitine to acyl CoA.
4. The carnitine released returns to cytosol for reuse.
Steps -2; Transport of fatty acid into mitochondria
8. Each cycle of β -oxidation, liberating a two carbon unit-acetyl CoA, occurs in a
sequence of four reactions
1. Oxidation
2. Hydration
3. Oxidation
4. Cleavage.
1. Oxidation
• Acyl CoA undergoes dehydrogenation by an FAD-dependent flavoenzyme, acyl
CoA dehydrogenase.
• A double bond is formed between α and β carbons (i.e., 2 and 3 carbons)
Steps -3; Beta-Oxidation proper
9. 2.Hydration:
• Enoyl CoA hydratase brings about the hydration of the double bond to form β -
hydroxyacyl CoA.
3.Oxidation
• β-Hydroxyacyl CoA dehydrogenase catalyses the second oxidation and
generates NADH.
• The product formed is β-ketoacyl CoA.
10. 4.Cleavage
• The final reaction in β -oxidation is the liberation of a 2 carbon fragment, acetyl
CoA from acyl CoA.
• This occurs by a thiolytic cleavage catalysed by β-ketoacyl CoA thiolase (or
thiolase).
The new acyl CoA, containing two carbons less than the original, reenters the β-
oxidation cycle.
The process continues till the fatty acid is completely oxidized.
12. Reference
Cox, Michael M., and David L. Nelson. Lehninger principles of
biochemistry. Vol. 5. New York: Wh Freeman, 2008.
Pranav, K., & Mina, U. (2013). Life Sciences: Fundamentals and
practice. New Delhi: Pathfinder Academy.
Satyanarayana, U. (2014). Metabolism of lipids.