Cell Structure and Function

Total Page:16

File Type:pdf, Size:1020Kb

Cell Structure and Function BIOLOGY Chapter 4: pp. 59-84 10th Edition Cell Structure and S. Sylvia Function Plasma membrane: outer surface that Ribosome: Fimbriae: regulates entrance site of protein synthesis hairlike bristles that and exit of molecules allow adhesion to Mader the surfaces Inclusion body: Conjugation pilus: stored nutrients for elongated, hollow later use appendage used for DNA transfer to other Nucleus: Mesosome: bacterial cells plasma membrane Cytoskeleton: maintains cell that folds into the Nucleoid: shape and assists cytoplasm and location of the bacterial movement of increases surface area chromosome cell parts: Endoplasmic Plasma membrane: reticulum: sheath around cytoplasm that regulates entrance and exit of molecules Cell wall: covering that supports, shapes, and protects cell Glycocalyx: gel-like coating outside cell wall; if compact, called a capsule; if diffuse, called a slime layer Flagellum: rotating filament present in some bacteria that pushes the cell forward *not in plant cells PowerPoint® Lecture Slides are prepared by Dr. Isaac Barjis, Biology Instructor 1 Copyright © The McGraw Hill Companies Inc. Permission required for reproduction or display Outline Cellular Level of Organization Cell theory Cell size Prokaryotic Cells Eukaryotic Cells Organelles Nucleus and Ribosome Endomembrane System Other Vesicles and Vacuoles Energy related organelles Cytoskeleton Centrioles, Cilia, and Flagella 2 Cell Theory Detailed study of the cell began in the 1830s A unifying concept in biology Originated from the work of biologists Schleiden and Schwann in 1838-9 States that: All organisms are composed of cells German botanist Matthais Schleiden in 1838 German zoologist Theodor Schwann in 1839 All cells come only from preexisting cells German physician Rudolph Virchow in 1850’s Cells are the smallest structural and functional unit of organisms 3 Organisms and Cells Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. a. c. b. 50 m d. 140 m a: © Geoff Bryant/Photo Researchers, Inc.; b: Courtesy Ray F. Evert/University of Wisconsin Madison; c: © Barbara J. Miller/Biological Photo Service; d: Courtesy O. Sabatakou and E. Xylouri-Frangiadak 4 Sizes of Living Things Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 0.1 nm 1 nm 10 nm 100 nm 1 m 10 m 100 m 1 mm 1 cm 0.1 m 1 m 10 m 100 m 1 km protein chloroplast plant and mouse rose animal frog egg amino cells acid virus ostrich most bacteria human egg ant egg atom blue whale electron microscope human light microscope human eye 5 Cell Size Cells range in size from one millimeter down to one micrometer Cells need a large surface area of plasma membrane to adequately exchange materials. The surface-area-to-volume ratio requires that cells be small Large cells - surface area relative to volume decreases Volume is living cytoplasm, which demands nutrients and produces wastes Cells specialized in absorption utilize membrane modifications such as microvilli to greatly increase surface area per unit volume 6 Surface to Volume Ratio Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. One 4-cm cube Eight 2-cm cubes Sixty-four 1-cm cubes Total surface area (height × width × number of sides × number of cubes) 96 cm2 192 cm2 384 cm2 Total volume (height × width × length × number of cubes) 64 cm3 64 cm3 64 cm3 Surface area: Volume per cube (surface area ÷ volume) 1.5:1 3:1 6:1 7 Microscopy Today: Compound Light Microscope Light passed through specimen Focused by glass lenses Image formed on human retina Max magnification about 1000X Resolves objects separated by 0.2 mm, 500X better than human eye 8 Compound Light Microscope Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 85 µ m amoeba, light micrograph eye ocular lens light rays objective lens specimen condenser lens light source a. Compound light microscope © Robert Brons/Biological Photo Service 9 Microscopy Today: Transmission Electron Microscope Abbreviated T.E.M. Electrons passed through specimen Focused by magnetic lenses Image formed on fluorescent screen Similar to TV screen Image is then photographed Max magnification 1000,000sX Resolves objects separated by 0.00002 mm, 100,000X better than human eye 10 Transmission Electron Microscope Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 200 nm pseudopod segment, transmission electron micrograph electron source electron beam electromagnetic condenser lens specimen electromagnetic objective lens electromagnetic projector lens observation screen or photographic plate b. Transmission electron microscope © M. Schliwa/Visuals Unlimited 11 Microscopy Today: Scanning Electron Microscope Abbreviated S.E.M. Specimen sprayed with thin coat of metal Electron beam scanned across surface of specimen Metal emits secondary electrons Emitted electrons focused by magnetic lenses Image formed on fluorescent screen Similar to TV screen Image is then photographed 12 Scanning Electron Microscope Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 500 µ m amoeba, scanning electron micrograph electron gun electron beam electromagnetic condenser lenses scanning coil final condenser electron lens detector secondary electrons TV specimen viewing screen c. Scanning electron microscope © Kessel/Shih/Peter Arnold, Inc. 13 Microscopy Today: Immunofluorescence Light Microscope Antibodies developed against a specific protein Fluorescent dye molecule attached to antibody molecules Specimen exposed to fluorescent antibodies Ultra-violet light (black light) passed through specimen Fluorescent dye glows in color where antigen is located Emitted light is focused by glass lenses onto human retina Allows mapping distribution of a specific protein in cell 14 Microscopy Today: Confocal Microscopy Narrow laser beam scanned across transparent specimen Beam is focused at a very thin plane Allows microscopist to optically section a specimen Sections made at different levels Allows assembly of 3d image on computer screen that can be rotated 15 Microscopy and Amoeba proteus Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 85 µ m 200 nm 500 µ m amoeba, light micrograph pseudopod segment, transmission electron amoeba, scanning electron micrograph micrograph electron source electron gun eye electron beam ocular lens electron beam light rays electromagnetic condenser lens electromagnetic condenserl enses specimen electromagnetic objective lens objective lens scanning coil specimen condenser lens final electromagnetic Condenser electron projector lens lens detector secondary observation screen electrons TV or specimen Viewing light source photographic plate screen a. Compound light microscope b. Transmission electron microscope c. Scanning electron microscope a: © Robert Brons/Biological Photo Service; b: © M. Schliwa/Visuals Unlimited; c: © Kessel/Shih/Peter Arnold, Inc. 16 Microscopy and Cheek Cells Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. 30 m 30 m 25 m 25 m 25 m Bright-field. Light Bright-field (stained). Differential interference Phase contrast. Density Dark-field. Light is passed passing through the Dyes are used to stain contrast. Optical methods differences in the through the specimen at specimen is brought the specimen. Certain are used to enhance specimen cause light rays an oblique angle so that directly into focus. Usually, components take up density differences within to come out of “phase.” the objective lens receives the low level of contrast the dye more than other the specimen so that The microscope enhances only light diffracted and within the specimen components, and therefore certain regions appear these phase differences so scattered by the object. interferes with viewing all contrast is enhanced. brighter than others. This that some regions of the This technique is used to but its largest components. technique is used to view specimen appear brighter view organelles, which living cells, chromosomes, or darker than others. The appear quite bright against and organelle masses. technique is widely used a dark field. to observe living cells and organelles. (Bright field): © Ed Reschke; (Bright field stained): © Biophoto Associates/Photo Researchers, Inc.; (Differential, Phase contrast, Dark field): © David M. Phillips/Visuals Unlimited 17 Prokaryotic Cells Lack a membrane-bound nucleus Structurally smaller and simpler than eukaryotic cells (which have a nucleus). Prokaryotic cells are placed in two taxonomic domains: Bacteria Archaea Live in extreme habitats Domains are structurally similar but biochemically different 18 The Structure of Bacteria Extremely small - 1–1.5 μm wide and 2–6 μm long Occur in three basic shapes: Spherical coccus, Rod-shaped bacillus, Spiral spirillum (if rigid) or spirochete (if flexible). Cell Envelope includes: Plasma membrane - lipid bilayer with imbedded and peripheral protein Form internal pouches (mesosomes) Cell wall - maintains the shape of the cell and is strengthened by peptidoglycan Glycocalyx - layer of polysaccharides on the outside of the cell wall Well organized and resistant to removal (capsule) 19 The Structure of Bacteria Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. spirillum spirochete bacillus coccus 20 The Structure
Recommended publications
  • Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
    Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal.
    [Show full text]
  • NIH Public Access Author Manuscript Mucosal Immunol
    NIH Public Access Author Manuscript Mucosal Immunol. Author manuscript; available in PMC 2014 March 01. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Mucosal Immunol. 2013 March ; 6(2): 379–392. doi:10.1038/mi.2012.81. Molecular Organization of the Mucins and Glycocalyx Underlying Mucus Transport Over Mucosal Surfaces of the Airways Mehmet Kesimer*,‡,▫, Camille Ehre*, Kimberly A. Burns*, C. William Davis*,†, John K. Sheehan*,‡, and Raymond J. Pickles*,§ *Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina, Chapel Hill, NC 27599-7248 ‡Department of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC 27599-7248 †Department of Cell and Molecular Physiology, University of North Carolina, Chapel Hill, NC 27599-7248 §Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599-7248 Abstract Mucus, with its burden of inspired particulates, and pathogens, is cleared from mucosal surfaces of the airways by cilia beating within the periciliary layer (PCL). The PCL is held to be ‘watery’ and free of mucus by thixotropic-like forces arising from beating cilia. With radii of gyration ~250 nm, however, polymeric mucins should reptate readily into the PCL, so we assessed the glycocalyx for barrier functions. The PCL stained negative for MUC5AC and MUC5B, but it was positive for keratan sulfate, a glycosaminoglycan commonly associated with glycoconjugates. Shotgun proteomics showed keratan sulfate-rich fractions from mucus containing abundant tethered mucins, MUC1, MUC4, and MUC16, but no proteoglycans. Immuno-histology by light and electron microscopy localized MUC1 to microvilli, MUC4 and MUC20 to cilia, and MUC16 to goblet cells.
    [Show full text]
  • Nanoarchitecture and Dynamics of the Mouse Enteric Glycocalyx Examined by Freeze-Etching Electron Tomography and Intravital Microscopy
    ARTICLE https://doi.org/10.1038/s42003-019-0735-5 OPEN Nanoarchitecture and dynamics of the mouse enteric glycocalyx examined by freeze-etching electron tomography and intravital microscopy Willy W. Sun1,2,5, Evan S. Krystofiak1,5, Alejandra Leo-Macias1, Runjia Cui1, Antonio Sesso3, Roberto Weigert 4, 1234567890():,; Seham Ebrahim4 & Bechara Kachar 1* The glycocalyx is a highly hydrated, glycoprotein-rich coat shrouding many eukaryotic and prokaryotic cells. The intestinal epithelial glycocalyx, comprising glycosylated transmembrane mucins, is part of the primary host-microbe interface and is essential for nutrient absorption. Its disruption has been implicated in numerous gastrointestinal diseases. Yet, due to chal- lenges in preserving and visualizing its native organization, glycocalyx structure-function relationships remain unclear. Here, we characterize the nanoarchitecture of the murine enteric glycocalyx using freeze-etching and electron tomography. Micrometer-long mucin filaments emerge from microvillar-tips and, through zigzagged lateral interactions form a three-dimensional columnar network with a 30 nm mesh. Filament-termini converge into globular structures ~30 nm apart that are liquid-crystalline packed within a single plane. Finally, we assess glycocalyx deformability and porosity using intravital microscopy. We argue that the columnar network architecture and the liquid-crystalline packing of the fila- ment termini allow the glycocalyx to function as a deformable size-exclusion filter of luminal contents. 1 Laboratory of Cell Structure and Dynamics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA. 2 Neuroscience and Cognitive Science Program, University of Maryland, College Park, MD 20740, USA. 3 Sector of Structural Biology, Institute of Tropical Medicine, University of São Paulo, Sao Paulo, SP 05403, Brazil.
    [Show full text]
  • Nomina Histologica Veterinaria, First Edition
    NOMINA HISTOLOGICA VETERINARIA Submitted by the International Committee on Veterinary Histological Nomenclature (ICVHN) to the World Association of Veterinary Anatomists Published on the website of the World Association of Veterinary Anatomists www.wava-amav.org 2017 CONTENTS Introduction i Principles of term construction in N.H.V. iii Cytologia – Cytology 1 Textus epithelialis – Epithelial tissue 10 Textus connectivus – Connective tissue 13 Sanguis et Lympha – Blood and Lymph 17 Textus muscularis – Muscle tissue 19 Textus nervosus – Nerve tissue 20 Splanchnologia – Viscera 23 Systema digestorium – Digestive system 24 Systema respiratorium – Respiratory system 32 Systema urinarium – Urinary system 35 Organa genitalia masculina – Male genital system 38 Organa genitalia feminina – Female genital system 42 Systema endocrinum – Endocrine system 45 Systema cardiovasculare et lymphaticum [Angiologia] – Cardiovascular and lymphatic system 47 Systema nervosum – Nervous system 52 Receptores sensorii et Organa sensuum – Sensory receptors and Sense organs 58 Integumentum – Integument 64 INTRODUCTION The preparations leading to the publication of the present first edition of the Nomina Histologica Veterinaria has a long history spanning more than 50 years. Under the auspices of the World Association of Veterinary Anatomists (W.A.V.A.), the International Committee on Veterinary Anatomical Nomenclature (I.C.V.A.N.) appointed in Giessen, 1965, a Subcommittee on Histology and Embryology which started a working relation with the Subcommittee on Histology of the former International Anatomical Nomenclature Committee. In Mexico City, 1971, this Subcommittee presented a document entitled Nomina Histologica Veterinaria: A Working Draft as a basis for the continued work of the newly-appointed Subcommittee on Histological Nomenclature. This resulted in the editing of the Nomina Histologica Veterinaria: A Working Draft II (Toulouse, 1974), followed by preparations for publication of a Nomina Histologica Veterinaria.
    [Show full text]
  • Mechanical Characterisation of Bone Cells and Their Glycocalyx
    Mechanical characterisation of bone cells and their glycocalyx a dissertation presented by Stefania Marcotti to The Department of Mechanical Engineering University of Sheffield Sheffield, United Kingdom in partial fulfilment of the requirements for the degree of Doctor of Philosophy Supervisor: Prof. Damien Lacroix Co-Supervisor: Dr. Gwendolen C Reilly November 2017 Abstract Mechanotransductionreferstotheprocessbywhichacellisabletotranslatemech- anical stimulation into biochemical signals. In bone, mechanotransduction regu- lates how cells detect environmental stimuli and use these to direct towards bone deposition or resorption. The mechanical properties of bone cells have an impact on the way mechanical stimulation is sensed, however, little evidence is available about how these properties influence mechanotransduction. The aim of the present Thesis was to quantify the mechanical properties of bone cells with a combined experimental and computational approach. Atomic force microscopy was employed to quantify the stiffness of bone cells and their gly- cocalyx. Changes in cell stiffness during osteocytogenesis were explored. Single molecule force spectroscopy of glycocalyx components was performed to evalu- ate their anchoring to the cytoskeleton. A single cell finite element model was designed to discern the contributions of sub-cellular components in response to simulated cell nano-indentation. Wide ranges of variation were found for bone cell stiffness and a method was proposed to determine suitable sample sizes to capture population heterogeneity. Bytargetingsinglecomponentsoftheboneglycocalyx, itwaspossibletohypothes- ise different mechanotransduction mechanisms depending on the hyaluronic acid attachment to the cytoskeleton. The developed computational framework showed similar results to the nano-indentation experiments and highlighted the role of the actin cytoskeleton in withstanding compression and distributing strain within the cell. iii Publications and conference presentations Book chapters Marcotti S and Reilly GC (2017).
    [Show full text]
  • Mesosomes in Escherichia Coli R
    JOURNAL OF BACTERIOLOGY, Jan. 1969, p. 367-375 Vol. 97, No. 1 Copyright @ 1969 American Society for Microbiology Printed in U.S.A. Mesosomes in Escherichia coli R. D. PONTEFRACT, G. BERGERON, AND F. S. THATCHER Research Laboratories, Food and Drug Directorate, Department of National Health and Welfare, Ottawa 3, Ontario, Canada Received for publication 19 October 1968 When Escherichia coli was grown in a synthetic medium and fixed with osmium, sections of the cells revealed clearly defined mesosomes. These mesosomes ap- peared to develop, in dividing cells, as coiled infoldings of the cytoplasmic mem- brane. Mature mesosomes formed a link between the cytoplasmic membrane and the nucleus of the cell. The arrangement of the mesosomes in dividing cells led to the hypothesis that division of the nucleus in these cells is accomplished by two separate polar mesosomes. One mesosome is derived from the parent cell and is present at one pole of the daughter cell. The other is freshly synthesized at or near the newly forming pole of the daughter cell. While the old mesosome remains at- tached to the chromosome received from the parent cell, the newly synthesized mesosome becomes attached to and initiates replication of the new chromosome. As the cell grows and elongates, the two mesosomes, attached to their respective chro- mosomes move apart, thus effecting nuclear division. Infoldings of the plasma membrane to form buffer with 0.1 M Ca++ (pH 6.1), progressively de- tubular structures, termed mesosomes by Fitz- hydrated in distilled acetone kept over a "molecular James (4), have been most commonly observed in sieve" (type 4A beads, Union Carbide Corp., Linde 5, Division, Ontario, Canada), and embedded in Epon gram-positive organisms (4, 14, 15).
    [Show full text]
  • Immuno-Electron and Confocal Laser Scanning Microscopy of the Glycocalyx
    biology Article Immuno-Electron and Confocal Laser Scanning Microscopy of the Glycocalyx Shailey Gale Twamley 1,2, Anke Stach 1, Heike Heilmann 3, Berit Söhl-Kielczynski 4, Verena Stangl 1,2, Antje Ludwig 1,2,*,† and Agnieszka Münster-Wandowski 3,*,† 1 Medizinische Klinik für Kardiologie und Angiologie, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany; [email protected] (S.G.T.); [email protected] (A.S.); [email protected] (V.S.) 2 DZHK (German Centre for Cardiovascular Research), Partner Site, 10117 Berlin, Germany 3 Institute of Integrative Neuroanatomy, Charité—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany; [email protected] 4 Institute for Integrative Neurophysiology—Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany; [email protected] * Correspondence: [email protected] (A.L.); [email protected] (A.M.-W.) † These authors equally contributed. Simple Summary: The glycocalyx (GCX) is a hydrated, gel-like layer of biological macromolecules attached to the cell membrane. The GCX acts as a barrier and regulates the entry of external substances into the cell. The function of the GCX is highly dependent on its structure and composition. Citation: Twamley, S.G.; Stach, A.; Pathogenic factors can affect the protective structure of the GCX. We know very little about the three- Heilmann, H.; Söhl-Kielczynski, B.; dimensional organization of the GXC. The tiny and delicate structures of the GCX are difficult Stangl, V.; Ludwig, A.; to study by microscopic techniques.
    [Show full text]
  • Characteristics of a Glycoprotein in the Ocular Surface Glycocalyx
    Investigative Ophthalmology & Visual Science, Vol. 33, No. 1, January 1992 Copyright © Association for Research in Vision and Ophthalmology Characteristics of a Glycoprotein in the Ocular Surface Glycocalyx llene K. Gipson,*t Michelle Yankauckas,* Sandra J. Spurr-Michaud,* Ann S. Tisdale,* and William Rineharr* A monoclonal antibody has been produced that binds to the apical squames (flattened cells) of the rat ocular surface epithelium and to the goblet cells of the conjunctiva. Immunoelectron microscopic localization of the antigen indicates that in apical cells it is present along the apical-microplical mem- brane in the region of the glycocalyx. In subapical squames, the antigen is in cytoplasmic vesicles. In some goblet cells, the antigen is in the Golgi network, and in others, it is located primarily in the membrane of the mucous granules. SDS-PAGE and immunoblot analysis demonstrate that the molecu- lar weight of the antigen is greater than 205 kD, and the electrophoretic band stains with Alcian blue followed by silver stain. Periodate oxidation of immunoblots and cryostat sections removes antibody binding. Neuraminidase treatment of cryostat sections does not remove antibody binding, whereas N-glycanase does. Taken together, these data indicate that the antigen recognized by the monoclonal antibody is a carbohydrate epitope on a high-molecular-weight, highly glycosylated glycoprotein in the glycocalyx of the ocular surface epithelium and goblet cell mucin granule membrane. The antigen appears to be stored within cytoplasmic vesicles and reaches the glycocalyx when cells differentiate to the apical-most position where the glycocalyx interfaces with the mucin layer of the tear film. Invest Ophthalmol Vis Sci 33:218-227,1992 The ocular surface epithelium that covers the con- tissue stained with tannic acid demonstrates that the junctiva and cornea is nonkeratinizing, stratified, and glycocalyx is a fine, filamentous layer.
    [Show full text]
  • Biol 1020: a Tour of the Cell
    Chapter 6: A Tour of the Cell Cell theory Cell organization and homeostasis Studying cells – microscopy and fractionation Eukaryotic vs. prokaryotic cells Compartments in eukaryotic cells (cell regions, organelles) Cytoskeleton Outside the cell . Chapter 6: A Tour of the Cell Cell theory Cell organization and homeostasis Studying cells – microscopy and fractionation Eukaryotic vs. prokaryotic cells Compartments in eukaryotic cells (cell regions, organelles) Cytoskeleton Outside the cell . • What are the main tenets of cell theory? • What are the major lines of evidence that all presently living cells have a common origin? . Cell theory All living organisms are composed of cells smallest “building blocks” of all multicellular organisms all cells are enclosed by a surface membrane that separates them from other cells and from their environment specialized structures with the cell are called organelles; many are membrane-bound . Cell theory Today, all new cells arise from existing cells All presently living cells have a common origin all cells have basic structural and molecular similarities all cells share similar energy conversion reactions all cells maintain and transfer genetic information in DNA the genetic code is essentially universal . • What are the main tenets of cell theory? • What are the major lines of evidence that all presently living cells have a common origin? . Chapter 6: A Tour of the Cell Cell theory Cell organization and homeostasis Studying cells – microscopy and fractionation Eukaryotic vs. prokaryotic cells Compartments in eukaryotic cells (cell regions, organelles) Cytoskeleton Outside the cell . • What is surface area to volume ratio, and why is it an important consideration for cells? • What (usually) happens to surface area to volume ratio as cells grow larger? .
    [Show full text]
  • University of Kirkuk/College of Nursing /Microbiology Introduction of Microbiology, and Bacterial Structure 1 Dr
    University of Kirkuk/College of nursing /Microbiology Introduction of microbiology, and bacterial structure 1 Dr. Gulbahar F. Karim ………………………………………………………………………………………………………………………………….. Lec.1// Introduction of microbiology, and bacterial structure Microbiology: is the science that deal with the study of microorganisms. Microorganisms can be found in every ecosystem, and in close association with every type of multicellular organisms. They populate the healthy human body by billions as normal flora. -Many scientist had rule in the development of this science including: -Louis Pasteur (1857) established that fermentation was the result of microbial activity. -Robert Koch (father of bacteriology) perfected bacteriological techniques during his studies on the culture of Bacillus anthraces (1876). He introduced staining techniques and also methods of obtaining bacteria in pure culture using solid media. He discovered Mycobacterium tuberculosis (1882), Vibrio cholerae (1883) -Fleming (1925) made the accidental discovery that the fungus penicillium produces a substance which destroys staphylococci. -Microbiology include many branches. Here we are concerned with medical microbiology. Medical microbiology (Gr. mikros-small, bios-life, logos-science) is the study of causative agents of infectious disease of human beings and their reactions to such infections. In other words it deals with etiology, pathogenesis, laboratory diagnosis, treatment, epidemiology and control of infection. It is studied under following headings: a. Parasitology ,Mycology , Immunology , Bacteriology, Genetics , and and Virology (which are consider between living and non living organisms). Microorganisms are classified under the kingdom Protista which is subdivided into two groups: 1-Eukaryotic organisms(with nucleus): include fungi, Algae, protozoa, helminthes. 2-Prokaryotic organisms(without nucleus): include bacteria and green algae. Morphology of bacteria: - Bacteria are unicellular,free living organisms ,live everywhere, present in soil, water.
    [Show full text]
  • Introduction to Microbiology
    Introduction to microbiology Prof. dr hab. Beata M. Sobieszczańska Department of Microbiology University of Medicine • http://www.lekarski.umed.wroc.pl/mikrobiologia • schedules, rules, important information • Consulting hours – teachers are always available for students during consulting hours or classes – apart from consulting hours – you must chase ! • Sick leaves (original) must be shown to the teacher just after an absence but not longer than after two weeks otherwise a sick note will not be honored - a copy of the sick note must be delivered to the secretary office • Class tests – 10 open questions • Terms: 1st, 2nd – if failed commission test from the whole material at the end of semester • Students with the average 4.8 will be released from the final exam • Presence on lectures and classes are obligatory • The final grade from classes is the average of all grades during semester Your best friend in this year: Medical Microbiology by Patrick R. Murray, Ken S. Rosenthal, Michael A. Pfaller Answer questions: • Name important cell wall structures of GP and GN bacteria • What is a role of these structures in human diseases? • Name other than bacterial cell wall structures and explain their role in bacterial pathogenicity • Do you understand the term pathogenicity? • Name five different genera GP and GN bacteria and indicate the colour they have after Gram staining Answer questions: • Name clinically important bacteria producing endospores – why endospores are important? • What is the difference between capsule and glycocalyx layer on GP bacteria? • What is axial filament? What role it plays? What bacteria produce axial filaments? • Name two types of pili and their role in bacterial pathogenicity Most bacteria come in one of three basic shapes: coccus, rod or bacillus & spiral MURRAY 7th ed.
    [Show full text]
  • Changes in the Ultrastructure of Staphylococcus Aureus Treated with Cationic Peptides and Chlorhexidine
    microorganisms Article Changes in the Ultrastructure of Staphylococcus aureus Treated with Cationic Peptides and Chlorhexidine Alina Grigor’eva, Alevtina Bardasheva, Anastasiya Tupitsyna, Nariman Amirkhanov , Nina Tikunova, Dmitrii Pyshnyi and Elena Ryabchikova * Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of Russian Academy of Science, Lavrent’ev av. 8, 630090 Novosibirsk, Russia; [email protected] (A.G.); [email protected] (A.B.); [email protected] (A.T.); [email protected] (N.A.); [email protected] (N.T.); [email protected] (D.P.) * Correspondence: [email protected]; Tel.: +7-383-363-51-63 Received: 11 November 2020; Accepted: 11 December 2020; Published: 14 December 2020 Abstract: Antimicrobial peptides, including synthetic ones, are becoming increasingly important as a promising tool to fight multidrug-resistant bacteria. We examined the effect of cationic peptides H2N-Arg9-Phe2-C(O)NH2 and H2N-(Lys-Phe-Phe)3-Lys-C(O)NH2 on Staphylococcus aureus, which remains one of the most harmful pathogens. Antiseptic chlorhexidine served as reference preparation. We studied viability of S. aureus and examined its ultrastructure under treatment with 100 µM of R9F2 or (KFF)3K peptides or chlorhexidine using transmission electron microscopy of ultrathin sections. Bacterial cells were sampled as kinetic series starting from 1 min up to 4 h of treatment with preparations. Both peptides caused clearly visible damage of bacteria cell membrane within 1 min. Incubation of S. aureus with R9F2 or (KFF)3K peptides led to cell wall thinning, loss of cytoplasm structure, formation of mesosome-derived multimembrane structures and “decorated fibers” derived from DNA chains.
    [Show full text]