The document is an assignment submission on the electron transport chain. It provides details on the electron transport chain, including that it is a series of protein complexes in the mitochondrial inner membrane that sequentially transfers electrons, pumping protons out in the process. This generates a proton gradient that is then used by ATP synthase to produce ATP via chemiosmosis, making oxidative phosphorylation the most efficient ATP producer in aerobic respiration. The assignment covers the components, steps, and purpose of the electron transport chain in detail over multiple pages.
The electron transport chain is comprised of a series of enzymatic reactions within the inner membrane of the mitochondria, which are cell organelles that release and store energy for all physiological needs.
As electrons are passed through the chain by a series of oxidation-reduction reactions, energy is released, creating a gradient of hydrogen ions, or protons, across the membrane. The proton gradient provides energy to make ATP, which is used in oxidative phosphorylation.
The electron transport chain is comprised of a series of enzymatic reactions within the inner membrane of the mitochondria, which are cell organelles that release and store energy for all physiological needs.
As electrons are passed through the chain by a series of oxidation-reduction reactions, energy is released, creating a gradient of hydrogen ions, or protons, across the membrane. The proton gradient provides energy to make ATP, which is used in oxidative phosphorylation.
Electron Transport Chain and oxidative phosphorylationusmanzafar66
substrate level phosphorylation and chemiosmosis
in Eukaryotes and in prokaryotes
in plant and animal
uncoupler oxidative phosphorylation
fat and protein ATP calculation
A simple outline of oxidative phosphorylation.. It explains the process, site of occurrence, components involved, source of electron carriers and inhibitors of the process.
Electron Transport Chain and oxidative phosphorylationusmanzafar66
substrate level phosphorylation and chemiosmosis
in Eukaryotes and in prokaryotes
in plant and animal
uncoupler oxidative phosphorylation
fat and protein ATP calculation
A simple outline of oxidative phosphorylation.. It explains the process, site of occurrence, components involved, source of electron carriers and inhibitors of the process.
ETC and Phosphorylation by Salman SaeedSalman Saeed
ETC and Phosphorylation lecture for Biology, Botany, Zoology, and Chemistry Students by Salman Saeed lecturer Botany University College of Management and Sciences Khanewal, Pakistan.
About Author: Salman Saeed
Qualification: M.SC (Botany), M. Phil (Biotechnology) from BZU Multan.
M. Ed & B. Ed from GCU Faisalabad, Pakistan.
B.Sc Micro II Microbial physiology Unit 2 Bacterial RespirationRai University
Respiration is the energy source to all living organism. Bacterial ETS system generates energy for bacteria in form of ATP using oxidative phosphorylation.
The ETC is a collection of proteins bound to the inner mitochondrial membrane and organic molecules, which electrons pass through in a series of redox reactions, and release energy. The energy released forms a proton gradient, which is used in chemiosmosis to make a large amount of ATP by the protein ATP-synthase.
Oxidative phosphorylation or electron transport-linked phosphorylation)- the metabolic pathway in which cells use enzymes to oxidize nutrients, thereby releasing the chemical energy stored within in order to produce adenosine triphosphate (ATP).
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_ETC and Oxidative phosphorylation.pptxAlisha Shaikh
The electrons generated from different metabolic pathways of the cell are channeled to the electron transport chain by electron acceptors. The electrons then contributes for the synthesis of ATP.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
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
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
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MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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ETC
1. Course Code: BIO-CHEM 207
Course Title: Metabolism-1
Assignment on #1
Electron Transport Chain
Submitted To:
Name: Mahbuba Ferdous
Lecturer
Department of Biochemistry
PRIMEASIA UNIVERSITY
Submitted By:
Name: Najmul Hasan Forhad
ID: 181-038-033
Section: Friday Batch Department: Biochemistry
PRIMEASIA UNIVERSITY
Date of Submission:15-04-2020
A missionwith a vision
2. Metabolism-1
AssaingmentNo- 1
Electron Transport Chain
Introduction
The electron transport chain is a series of proteins and organic molecules found in the inner membrane
of the mitochondria. Electrons are passed from one member of the transport chain to another in a series
of redox reactions. Energy released in these reactions is captured as a proton gradient, which is then
used to make ATP in a process called chemiosmosis. Together, the electron transport chain and
chemiosmosis make up oxidative phosphorylation.
The mitochondrial electron transport chain is a series of enzymes and coenzymes in the crista
membrane, each of which is reduced by the preceding coenzyme, and in turn reduces the next, until
finally the protons and electrons that have entered the chain from either NADH or reduced flavin reduce
oxygen to water.
Fundamentals
Aerobic cellular respiration made up of 3 parts: glycolysis, the Krebs cycle, and oxidative
phosphorylation. In glycolysis, glucose is metabolized into 2 molecules of pyruvate, with an output of
ATP and nicotinamide adenine dinucleotide (NADH). The pyruvate is oxidized into acetyl CoA and
NADH and carbon dioxide (CO2). The acetyl CoA is then used in the Krebs cycle, also known as the
citric acid cycle, which is a chain of chemical reactions that produce CO2, NADH, flavin adenine
3. dinucleotide (FADH2), and ATP. In the final step, the NADH, FADH2 amassed from the previous steps
is used in oxidative phosphorylation, to make water and ATP.
Oxidative phosphorylation is made up of 2 parts: the electron transport chain (ETC) and chemiosmosis.
The ETC is a collection of proteins and organic molecules, which electrons pass through in a series of
redox reactions, and release energy. The energy released forms a proton gradient, which is used in
chemiosmosis to make a large amount of ATP.
Photosynthesis is a metabolic process that converts light energy into chemical energy, to build sugars. In
the light-dependent reactions, light energy and water are used to make ATP, NADPH, and oxygen (O2).
The proton gradient used to make the ATP is formed via an electron transport chain. In the light-
independent reactions, sugar is made from the ATP and NADPH from the previous reactions.
Components of ETC:
NAD & Flavoprotein : H-carriers in celluiar respiration
Non heme metalloprotein (Fe-S- Protein):iron cycles between 3+ and 2+ states.
Ubiquinone or CoQ: region serves as an anchor to inner mitochondrial membrane.
Cytochromes : Electron-transfer proteins that contain a heme prosthetic group
Composition of ETC
Four large protein complexes.
Complex I - NADH-Coenzyme Q reductase
Complex II - Succinate-Coenzyme Q reductase
Complex III - Cytochrome c reductase
Complex IV - Cytochrome c oxidase
Many of the components are proteins with prosthetic
4. groups to move electrons
Steps of Oxidative phosphorylation & Electron Transport Chain
Oxidative phosphorylation is the process where energy is harnessed through a series of protein
complexes embedded in the inner-membrane of mitochondria (called the electron transport chain and
ATP synthase) to create ATP. Oxidative phosphorylation can be broken down into two parts: 1)
Oxidation of NADH and FADH2, and 2) Phosphorylation - the production of ATP
1.Oxidation of NADH and FADH2.- losing elctrons via high energy molecules :
Step 1
Oxidative phosphorylation starts with the arrival of 3 NADH and 1 FADH2 the citric acid cycle,
which shuttle high energy molecules to the electron transport chain. NADH transfers its high energy
molecules to protein complex 1, while FADH2 2, transfers its high energy molecules to protein
complex 2. Shuttling high energy molecules causes a loss of electrons from NADH and FADH2
called oxidation (other molecules are also capable of being oxidized).
The opposite of oxidation is reduction, where a molecule gains electrons (which is seen in the
citric acid cycle)
5. Step 2 -
Hitting the gym to pump some serious hydrogens ;
The process of NADH oxidation leads to the pumping of protons through protein complex 1
from the matrix to the intermembrane space. The electrons that were received by protein
complex 1 are given to another membrane-bound electron carrier called ubiquinone or Q.
This process of transferring electrons drives the pumping of protons, which is seen as
unfavorable. Electron transfer driving proton pumping is repeated in complexes 3 and 4 (which
we will discuss in steps 2 - 5). As this action is repeated, protons will accumulate in the
intermembrane space. This accumulation of protons is how the cell temporarily stores
transformed energy.
Step-3
The rest of the steps are now the same for the high energy molecules from NADH and FADH2 in
earlier steps. Inside the nonpolar region of the phospholipid bilayer UQH2 (which is also a nonpolar
6. compound) transports the electrons to protein complex 3. UQH2 also carries protons. When end UQH2
dlivers electrons to protein complex 3, it also donates its protons to be pumped.
Step 4
The electrons that arrived at protein complex 3 are picked up by cytochrome C(or “cyt C”), the last
electron carrier. This action also causes protons to be pumped into the intermembrane space.
Step-5
Cytochrome C carries the electrons to the final protein complex, protein complex 4. Once again, energy
released via electron shuttling allows for another proton to be pumped into the intermembrane space.
The electrons are then drawn to oxygen, which is the final electron acceptor. Its important to note that
oxygen must be present for oxidative phosphorylation to occur. Water is formed as oxygen receives the
electrons from protein complex 4, and combines with protons on the inside of the cell.
7. 2. Phosphorylation - the production of ATP
Step 6
As a result of part 1 (Oxidation of NADH and , FADH2 an electrochemical gradient is created, meaning
there is a difference in electrical charge between the two sides of the inner mitochondrial membrane.
The outside, or exterior, of the mitochondrial membrane is positive because of the accumulation of the
protons), and the inside is negative due to the loss of the protons. A chemical concentration gradient has
also developed on either side of the membrane. The electrochemical gradient is how the cell transfers
the stored energy from the reduced NADH and FADH2.
8. Synthase of ATP :
When there is a high concentration of protons on the outside of the mitochondrial membrane, protons
are pushed through ATP synthase. This movement of protons causes ATP synthase to spin, and bind
ADP and Pi, producing ATP. Finally, ATP is made!
ATP synthase uses the proton gradient across the mitochondrial membrane to form ATP. It is made up
of F0 and F1 subunits which act as a rotational motor system. F0 portion is embedded in the
mitochondrial membrane and is protonated and deprotonated repeatedly causing it to rotate. This
rotation catalyzes the formation of ATP from ADP and Pi. The F1 portion works to hydrolyze the ATP.
A proton pump is any process that creates a proton gradient across a membrane. Protons can be
physically moved across a membrane; this is seen in mitochondrial Complexes I and IV. The same
effect can be produced by moving electrons in the opposite direction. The result is the disappearance of
a proton from the cytoplasm and the appearance of a proton in the periplasm. Mitochondrial Complex III
uses this second type of proton pump, which is mediated by a quinone (the Q cycle).
Some dehydrogenases are proton pumps; others are not. Most oxidases and reductases are proton pumps,
but some are not. Cytochrome bc1 is a proton pump found in many, but not all, bacteria (it is not found
in E. coli). As the name implies, bacterial bc1 is similar to mitochondrial bc1 (Complex III).
Proton pumps are the heart of the electron transport process. They produce the transmembrane
electrochemical gradient that enables ATP Synthase to synthesize ATP.
9. Summary
Oxidative phosphorylation is comprised of the electron transport chain and chemiosmosis.
It is the most efficient producer of ATP in the process of aerobic respiration
Electrons carried from previous steps of respiration enter the electron transport chain, and are
sequentially passed through membrane bound proteins
The final member of the chain is oxygen, which forms water upon accepting the electron
The electron transport chain generates a protein gradient
The protein gradient drives ATP synthase activity, which generates ATP
Nazmul Hasan Forhad
BSc. In Biochemistry
Prime Asia University,Dhaka
Email: forhad1767@gmail.com
Mobi:+8801926249001