This document provides an overview of bacterial cell structure and components. It discusses that bacteria are single celled organisms enclosed by a membrane. The key components of a bacterial cell include: proteins, nucleic acids, lipids and polysaccharides. Bacteria exhibit characteristics of living things like metabolism, reproduction, differentiation and communication. Structures inside and on the bacterial cell include flagella, fimbriae, cell wall, cell membrane, capsule, periplasm and cytoplasm. The document describes the differences between gram positive and gram negative cell walls.
Detailed description about bacteria cell structure and various cell organelles present in the bacterial cell has been presented in well described manner
Introduction-Cell wall and functions
Gram +ve and -ve cell wall
Bacterial cell wall - structure
Peptidoglycan-Composition and Structure
Types of polysaccharidesBacterial cell wall
Functions of polysaccharides in Bacterial cell wall
Detailed description about bacteria cell structure and various cell organelles present in the bacterial cell has been presented in well described manner
Introduction-Cell wall and functions
Gram +ve and -ve cell wall
Bacterial cell wall - structure
Peptidoglycan-Composition and Structure
Types of polysaccharidesBacterial cell wall
Functions of polysaccharides in Bacterial cell wall
General overview of Plasma/ Cell membrane.
Definition of Plasma/ Cell membrane
Structure of Plasma membrane
1. Sandwitch model ORDanielli- Davson Model
2. Fluid mosaic model
Plasma Membrane Proteins
Chemical Composition of Plasma/ Cell Membrane
Movement across the Cell Membrane
Channels through cell membrane
"Plasma membrane structure and function"
Presented by :
Jitul Kalita
Department of biotechnology,
Pandu College, Guwahati, Assam
jitulkalitaown@gmail.com
General overview of Plasma/ Cell membrane.
Definition of Plasma/ Cell membrane
Structure of Plasma membrane
1. Sandwitch model ORDanielli- Davson Model
2. Fluid mosaic model
Plasma Membrane Proteins
Chemical Composition of Plasma/ Cell Membrane
Movement across the Cell Membrane
Channels through cell membrane
"Plasma membrane structure and function"
Presented by :
Jitul Kalita
Department of biotechnology,
Pandu College, Guwahati, Assam
jitulkalitaown@gmail.com
Bacteria- Bacteria, the oldest and most diversified creatures on our planet, have a structure that is both basic and interesting.
Key points-
cell envelope- Investigate the bacterial cell's outermost layers, including the cell wall, cell membrane, and any other components that defend and preserve cell integrity.
cytoplasm and nucleotide- Discover the inner workings of bacterial cells, where genetic material is stored, metabolism occurs, and critical functions are organised.
Appandages and Flagella-Learn about the many appendages that bacteria can have, such as flagella, pili, and fimbriae, and how they help in motility and adherence.
Inclusions and Granules:Learn how bacteria adapt to their surroundings by storing energy and critical chemicals in the form of inclusions and granules.
Structural variation-Explore the variety of bacterial structure across various species and how these changes contribute to their adaptation and success.
Interactions and Ecological Importance: Investigate how bacteria's structure effects their interactions with other species and their significance in ecosystems.
This slide is presented by
Deepti Negi
Assistant professor
Pharmacology
Shri Guru Ram Rai University
Dehradun
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
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.
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
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
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
2. Cell
Fundamental unit of life
A single cell is isolated from other cells by a
membrane and contain within it chemicals and
subcellular structure.
Compartmentalization is a prerequisite for life
3. Cell chemistry
Chemical components
Proteins
Nucleic acids
Lipids
Polysaccharides
Collectively are called: Macromolecules
4. Characteristics of living system
Metabolism
Reproduction or Growth
Differentiation
Communication (Quorum Sensing)
Movement
Evolution
7. Flagella
Are filamentous protein structures attached to the cell
surface that provide the swimming movement for most
motile prokaryotes.
Prokaryotic flagella are much thinner than eukaryotic
flagella.
Diameter of a prokaryotic flagellum is about 20
nanometers
11. Fimbriae and pilli
• Heavy hair-like structures made of protein
• Fimbriae and pilli are interchangeable terms
- Composed of protein.
• Fimbriae are shorter and than flagella, and slightly
smaller in diameter.
• Nothing to do with bacterial movement.
12. Fimbriae and pilli
Are common in Gram-negative bacteria
Fimbriae are most often involved in adherence
In E. coli, a specialized type of pilus, the F or sex
pilus,
- numerous common pilli is quite different
15. Capsule
Polysaccharide layer outside of the cell wall polymer.
A true capsule is a discrete detectable layer of
polysaccharides deposited outside the cell wall.
A less discrete structure or matrix which embeds the
cells is a called a slime layer or a biofilm.
20. Function of capsule
Like fimbriae, slime layers, and glycocalyx,
capsules, often
- mediate adherence of cells to surfaces.
Capsules also protect bacterial cells from
engulfment
21. Function of capsule
Capsules in certain soil bacteria protect cells
from effects of drying or desiccation.
Capsular materials (e.g. dextrans) reserves of
carbohydrate for subsequent metabolism.
22. Cell wall
Maintains the overall shape of the bacteria cell
They are an essential structure for viability
They are composed of unique components found
nowhere else in nature.
They are one of the most important sites for attack
by antibiotics.
23. Cell wall
They provide ligands for adherence and receptor
sites for drugs or viruses.
They provide for immunological distinction and
immunological variation among strains of bacteria.
25. Peptidoglycan
Peptidoglycan is a complex polymer consisting, of three
parts:
a backbone composed of alternating N-
acetylglucosamine and N-acetylmuramic acid;
a set of identical tetrapeptide side chains
and peptide cross-bridges
26.
27. Gram-positive
Contain teichoic and teichuronic acids
Account for up to 50% of the dry weight of the wall and
10% of the dry weight of the total cell.
In addition, some gram-positive walls may contain
polysaccharide molecules.
There are two types of teichoic acids: wall teichoic acid
(WTA), and membrane teichoic acid a.k.a lipoteichoic
acids (LTA).
31. Structure of LPS
O-antigen a complex polysaccharide,
- composed of repeating units of five to eight
monosaccharides (galactose, rhamnose, mannose)
Core oligosaccharride
Lipid A
32. Plasma membrane
Is the most dynamic structure of a prokaryotic cell.
Main function is a s a selective permeability barrier
It sequesters the molecules of life in a unit, separating it
from the environment.
It allows passage of water and uncharged molecules up
to mw of about 100 daltons.
37. The Periplasm
Between the inner (plasma) and outer membranes of
Gram-negative bacteria and spirochetes.
The peptidoglycan sheet resides within the periplasm.
The periplasm is a very active compartment of the
cell.
38.
39. Cytoplasm
• Consists of an aqueous solution of three groups of
molecules:
• macromolecules such as proteins (enzymes), mRNA
and tRNA;
• small molecules that are energy sources, precursors
of macromolecules, metabolites or vitamins;
• various inorganic ions and cofactors
• The primary structural components found in the
cytoplasm are the nucleoid and ribosomes, and possibly
some type of inclusion.
43. Endospore
A bacterial structure sometimes observed as an
inclusion is actually a type of dormant cell.
Bacillus
Clostridium.
Thermoactinomyces,
Sporolactobacillus,
Sporosarcina,
Sporotomaculum,
Sporomusa,
Sporohalobacter.
44. Why spores are heat
resistance?
Dehydrated state.
The presence in the core of large amounts (5–15% of
the spore dry weight) of calcium dipicolinate.