Cell Membrane

Total Page:16

File Type:pdf, Size:1020Kb

Cell Membrane John Lenyo Corrina Perez Hazel Owens Cell Membrane http://micro.magnet.fsu.edu/cells/plasmamembrane/plasmamembrane.html • Cell membranes are composed of proteins and lipids. • Since they are made up of mostly lipids, only certain substances can move through. spmbiology403.blogspot.com •Phospholipids are the most abundant type of lipid found in the membrane. Phospholipids are made up of two layers, the outer and inner layers. The inside layer is made of hydrophobic fatty acid tails, while the outer layer is made up of hydrophilic polar heads that are pointed toward the water. academic.brooklyn.cuny.edu •Membrane structure relies on the tendency of fatty acid molecules to spread on the surface of water. • Membrane proteins (which take up half of the membrane) determine what gets into and leaves the cell. •Glycolipids are found on the outer part of the cell membrane. Single Chain vs. Phospholipid • Single chain lipids were assumed to be the first of those to form cell membranes with the more complex phospholipids evolving later • Phospholipids can be synthesized in an abiotic environment without enzymes now • Phosphoplipid bilayers now make up the plasma cell membranes that regulate movement into and out of prokaryotic and eukaryotic cells. Single chain lipid http://web.nestucca.k12.or.us/nvhs/staff/whitehead/homewor http://clincancerres.aacrjournals.org/content/11/5/2018/F1. k.htm expansion Types of Lipids • Today Plasma Membranes are made primarily of phospholipids • It is thought that early membranes may have been made of simpler fatty acids. http://exploringorigins.org/fattyacids.html Properties of Fatty Acids • They are Ampipathic, meaning that they have a hydrophobic (“water hating”) end and a hydrophilic (water loving”) end. •Hydrophobic molecules are nonpolar. They prefer other neutral or non‐polar molecules and avoid polar molecules, such as water. i.e. oil and vinegar http://www.cool‐science‐fair‐experiments.com/oil‐and‐vinegar‐separation‐ experimen/ •When fatty acids or phospholipids are put into an aqueous solution, they will self‐assemble into a ball. Their hydrophobic ends will face inward and hydrophilic Micelles • Micelles are basically spheres of fatty acids. • They will self‐assemble in an aqueous solution in low concentrations • Their hydrophilic ends point outward making contact with the water and the hydrophobic http://en.wikipedia.org/wiki/File:Micelle_scheme‐en.svg ends cluster together. Vesicles • Research from the Stoztak Lab at Massachusetts General Hospital has shown that micelles can form vesicles under the right conditions (pH, concentration, etc.) (http://genetics.mgh.harvard.edu/szostakweb/researchVesicles.html ) http://en.wikipedia.org/wiki/File:Lip osome_scheme‐en.svg •Vesicles are membrane‐enclosed sacks that form in aqueous solutions (http://en.wikipedia.org/wiki/Vesicle_(biology) ) •Once formed, phospholipid vesicles are highly stable •Fatty acid lipids are much more dynamic (http://exploringorigins.org/fattyacids.html ) Early Vesicles • Vesicles made of fatty acids are stable, but very dynamic. Fatty acids are constantly flipping in and out of the membrane. • This may have provided the opportunity for other monomers or macromolecules to enter the vesicle. http://genetics.mgh.harvard.edu/szostakweb/exploringOriginsDownloads/p rotocell.jpg Vesicle Research • In a cooperative effort from Harvard and other genetic research institutions efforts are being made to replicate working vesicles from plasma membranes. http://genetics.mgh.harvard.edu/szostakweb/researchVesicles.html http://www.hms.harvard.edu/dms/prospective/AboutDMS.html Early Earth • Some scientists propose that early earth had the capacity to form fatty acids, most likely near hydrothermal vents • Clays are thought to have played a role in catalyzing the formation of fatty acid tails from H and CO2 gases. • In large enough quantities, these fatty acids have been shown to self‐assemble into micelles, or vesicles (http://exploringorigins.org/fattyacids.html ) Early Earth • Research has shown that the clay montmorillonite can catalyze the formation of vesicle formation (http://exploringorigins.org/fattyacids.html ) • The vesicle is crucial to the formation of the protocell and is thought to be the precursor to the cell membrane • Today, however, plasma membranes are synthesized and regulated by the cell. Cell Membranes and Technology • European Researcher Pascal Jonkheijm is working to create artificial cell membranes on microchips to better understand how cells communicate with each other • Jonkheijm believes that the knowledge he gains can be a stepping stone into regenerative research. http://www.nanowerk.com/news/newsid=18101.php http://www.utnieuws.utwente.nl/new/?artikel_id=76814.
Recommended publications
  • Bacterial Cell Membrane
    BACTERIAL CELL MEMBRANE Dr. Rakesh Sharda Department of Veterinary Microbiology NDVSU College of Veterinary Sc. & A.H., MHOW CYTOPLASMIC MEMBRANE ➢The cytoplasmic membrane, also called a cell membrane or plasma membrane, is about 7 nanometers (nm; 1/1,000,000,000 m) thick. ➢It lies internal to the cell wall and encloses the cytoplasm of the bacterium. ➢It is the most dynamic structure of a prokaryotic cell. Structure of cell membrane ➢The structure of bacterial plasma membrane is that of unit membrane, i.e., a fluid phospholipid bilayer, composed of phospholipids (40%) and peripheral and integral proteins (60%) molecules. ➢The phospholipids of bacterial cell membranes do not contain sterols as in eukaryotes, but instead consist of saturated or monounsaturated fatty acids (rarely, polyunsaturated fatty acids). ➢Many bacteria contain sterol-like molecules called hopanoids. ➢The hopanoids most likely stabilize the bacterial cytoplasmic membrane. ➢The phospholipids are amphoteric molecules with a polar hydrophilic glycerol "head" attached via an ester bond to two non-polar hydrophobic fatty acid tails. ➢The phospholipid bilayer is arranged such that the polar ends of the molecules form the outermost and innermost surface of the membrane while the non-polar ends form the center of the membrane Fluid mosaic model ➢The plasma membrane contains proteins, sugars, and other lipids in addition to the phospholipids. ➢The model that describes the arrangement of these substances in lipid bilayer is called the fluid mosaic model ➢Dispersed within the bilayer are various structural and enzymatic proteins, which carry out most membrane functions. ➢Some membrane proteins are located and function on one side or another of the membrane (peripheral proteins).
    [Show full text]
  • Construction and Loss of Bacterial Flagellar Filaments
    biomolecules Review Construction and Loss of Bacterial Flagellar Filaments Xiang-Yu Zhuang and Chien-Jung Lo * Department of Physics and Graduate Institute of Biophysics, National Central University, Taoyuan City 32001, Taiwan; [email protected] * Correspondence: [email protected] Received: 31 July 2020; Accepted: 4 November 2020; Published: 9 November 2020 Abstract: The bacterial flagellar filament is an extracellular tubular protein structure that acts as a propeller for bacterial swimming motility. It is connected to the membrane-anchored rotary bacterial flagellar motor through a short hook. The bacterial flagellar filament consists of approximately 20,000 flagellins and can be several micrometers long. In this article, we reviewed the experimental works and models of flagellar filament construction and the recent findings of flagellar filament ejection during the cell cycle. The length-dependent decay of flagellar filament growth data supports the injection-diffusion model. The decay of flagellar growth rate is due to reduced transportation of long-distance diffusion and jamming. However, the filament is not a permeant structure. Several bacterial species actively abandon their flagella under starvation. Flagellum is disassembled when the rod is broken, resulting in an ejection of the filament with a partial rod and hook. The inner membrane component is then diffused on the membrane before further breakdown. These new findings open a new field of bacterial macro-molecule assembly, disassembly, and signal transduction. Keywords: self-assembly; injection-diffusion model; flagellar ejection 1. Introduction Since Antonie van Leeuwenhoek observed animalcules by using his single-lens microscope in the 18th century, we have entered a new era of microbiology.
    [Show full text]
  • Endoplasmic Reticulum-Plasma Membrane Contact Sites Integrate Sterol and Phospholipid Regulation
    RESEARCH ARTICLE Endoplasmic reticulum-plasma membrane contact sites integrate sterol and phospholipid regulation Evan Quon1☯, Yves Y. Sere2☯, Neha Chauhan2, Jesper Johansen1, David P. Sullivan2, Jeremy S. Dittman2, William J. Rice3, Robin B. Chan4, Gilbert Di Paolo4,5, Christopher T. Beh1,6*, Anant K. Menon2* 1 Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia, Canada, 2 Department of Biochemistry, Weill Cornell Medical College, New York, New York, United States of a1111111111 America, 3 Simons Electron Microscopy Center at the New York Structural Biology Center, New York, New a1111111111 York, United States of America, 4 Department of Pathology and Cell Biology, Columbia University College of a1111111111 Physicians and Surgeons, New York, New York, United States of America, 5 Denali Therapeutics, South San a1111111111 Francisco, California, United States of America, 6 Centre for Cell Biology, Development, and Disease, Simon a1111111111 Fraser University, Burnaby, British Columbia, Canada ☯ These authors contributed equally to this work. * [email protected] (AKM); [email protected] (CTB) OPEN ACCESS Abstract Citation: Quon E, Sere YY, Chauhan N, Johansen J, Sullivan DP, Dittman JS, et al. (2018) Endoplasmic Tether proteins attach the endoplasmic reticulum (ER) to other cellular membranes, thereby reticulum-plasma membrane contact sites integrate sterol and phospholipid regulation. PLoS creating contact sites that are proposed to form platforms for regulating lipid homeostasis Biol 16(5): e2003864. https://doi.org/10.1371/ and facilitating non-vesicular lipid exchange. Sterols are synthesized in the ER and trans- journal.pbio.2003864 ported by non-vesicular mechanisms to the plasma membrane (PM), where they represent Academic Editor: Sandra Schmid, UT almost half of all PM lipids and contribute critically to the barrier function of the PM.
    [Show full text]
  • Cell Wall Constrains Lateral Diffusion of Plant Plasma-Membrane Proteins
    Cell wall constrains lateral diffusion of plant SEE COMMENTARY plasma-membrane proteins Alexandre Martinièrea, Irene Lavagia, Gayathri Nageswarana, Daniel J. Rolfeb, Lilly Maneta-Peyretc, Doan-Trung Luud, Stanley W. Botchwayb, Stephen E. D. Webbb, Sebastien Mongrandc, Christophe Maureld, Marisa L. Martin-Fernandezb, Jürgen Kleine-Vehne, Jirí Frimlf, Patrick Moreauc, and John Runionsa,1 aDepartment of Biological and Medical Sciences, Oxford Brookes University, Oxford OX3 0BP, United Kingdom; bCentral Laser Facility, Research Complex at Harwell, Science and Technology Facilities Council, Rutherford Appleton Laboratory, Oxfordshire OX11 0QX, United Kingdom; cLaboratoire de Biogenèse Membranaire, Unité Mixte de Recherche 5200 Centre National de la Recherche Scientifique, Université Bordeaux Segalen, 33076 Bordeaux, France; dLaboratoire de Biochimie et Physiologie Moléculaire des Plantes, Institut de Biologie Intégrative des Plantes, Unité Mixte de Recherche 5004, Centre National de la Recherche Scientifique/Unité Mixte de Recherche 0386 Institut National de la Recherche Agronomique, 34060 Montpellier, France; eDepartment of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, 1190 Vienna, Austria; and fDepartment of Plant Biotechnology and Genetics, Ghent University, 9052 Ghent, Belgium Edited by Daniel J. Cosgrove, Pennsylvania State University, University Park, PA, and approved May 16, 2012 (received for review February 3, 2012) A cell membrane can be considered a liquid-phase plane in which yeast lines lacking
    [Show full text]
  • An Overview of Lipid Membrane Models for Biophysical Studies
    biomimetics Review Mimicking the Mammalian Plasma Membrane: An Overview of Lipid Membrane Models for Biophysical Studies Alessandra Luchini 1 and Giuseppe Vitiello 2,3,* 1 Niels Bohr Institute, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen, Denmark; [email protected] 2 Department of Chemical, Materials and Production Engineering, University of Naples Federico II, Piazzale Tecchio 80, 80125 Naples, Italy 3 CSGI-Center for Colloid and Surface Science, via della Lastruccia 3, 50019 Sesto Fiorentino (Florence), Italy * Correspondence: [email protected] Abstract: Cell membranes are very complex biological systems including a large variety of lipids and proteins. Therefore, they are difficult to extract and directly investigate with biophysical methods. For many decades, the characterization of simpler biomimetic lipid membranes, which contain only a few lipid species, provided important physico-chemical information on the most abundant lipid species in cell membranes. These studies described physical and chemical properties that are most likely similar to those of real cell membranes. Indeed, biomimetic lipid membranes can be easily prepared in the lab and are compatible with multiple biophysical techniques. Lipid phase transitions, the bilayer structure, the impact of cholesterol on the structure and dynamics of lipid bilayers, and the selective recognition of target lipids by proteins, peptides, and drugs are all examples of the detailed information about cell membranes obtained by the investigation of biomimetic lipid membranes. This review focuses specifically on the advances that were achieved during the last decade in the field of biomimetic lipid membranes mimicking the mammalian plasma membrane. In particular, we provide a description of the most common types of lipid membrane models used for biophysical characterization, i.e., lipid membranes in solution and on surfaces, as well as recent examples of their Citation: Luchini, A.; Vitiello, G.
    [Show full text]
  • Membrane Proteins Are Associated with the Membrane of a Cell Or Particular Organelle and Are Generally More Problematic to Purify Than Water-Soluble Proteins
    Strategies for the Purification of Membrane Proteins Sinéad Marian Smith Department of Clinical Medicine, School of Medicine, Trinity College Dublin, Ireland. Email: [email protected] Abstract Although membrane proteins account for approximately 30 % of the coding regions of all sequenced genomes and play crucial roles in many fundamental cell processes, there are relatively few membranes with known 3D structure. This is likely due to technical challenges associated with membrane protein extraction, solubilization and purification. Membrane proteins are classified based on the level of interaction with membrane lipid bilayers, with peripheral membrane proteins associating non- covalently with the membrane, and integral membrane proteins associating more strongly by means of hydrophobic interactions. Generally speaking, peripheral membrane proteins can be purified by milder techniques than integral membrane proteins, whose extraction require phospholipid bilayer disruption by detergents. Here, important criteria for strategies of membrane protein purification are addressed, with a focus on the initial stages of membrane protein solublilization, where problems are most frequently are encountered. Protocols are outlined for the successful extraction of peripheral membrane proteins, solubilization of integral membrane proteins, and detergent removal which is important not only for retaining native protein stability and biological functions, but also for the efficiency of downstream purification techniques. Key Words: peripheral membrane protein, integral membrane protein, detergent, protein purification, protein solubilization. 1. Introduction Membrane proteins are associated with the membrane of a cell or particular organelle and are generally more problematic to purify than water-soluble proteins. Membrane proteins represent approximately 30 % of the open-reading frames of an organism’s genome (1-4), and play crucial roles in basic cell functions including signal transduction, energy production, nutrient uptake and cell-cell communication.
    [Show full text]
  • DNA Extraction
    DNA Extraction Learning Objectives: Students learn about DNA, cell structure, and basic chemical separations. GRADE LEVEL SNEAK PEAK inside … ACTIVITY 4–8 Students extract DNA from strawberries. SCIENCE TOPICS STUDENT SUPPLIES Solutions and Mixtures see next page for more supplies Techniques strawberries Organic and Biochemistry sealing plastic bags dish soap PROCESS SKILLS salt meat tenderizer Describing and Defining isopropyl alcohol, etc…. Explaining Evaluating ADVANCE PREPARATION see next page for more details GROUP SIZE dilute soap mix tenderizer and salt together, etc…. 1–3 OPTIONAL EXTRAS DEMONSTRATION If available, goggles are recommended for this activity. Modeling the Procedure (p. C - 22) EXTENSIONS Animal DNA (p. C - 29) Other DNA Sources (p. C - 30) TIME REQUIRED Advance Preparation Set Up Activity Clean Up 15 minutes 15 minutes 20 minutes 15 minutes the day before DNA Extraction C – 19 Chemistry in the K–8 Classroom Grades 4–8 2007, OMSI SUPPLIES Item Amount Needed strawberries 1 per group sealing plastic bags (e.g., ZiplocTM) 1 per group liquid dish soap ½ teaspoon per group 99% isopropyl alcohol (or lower, e.g., 70% ¼ cup per group rubbing alcohol) meat tenderizer 1 tablespoon per class OR OR papaya or pineapple juice ¼ cup juice per class salt 1 tablespoon per class tall, clear, narrow plastic cups (8 oz. or 12 oz.) 2 per group plastic spoon 1 per group pop-top squeeze bottles (e.g., water or sports drink) 1 per group freezer or bucket of ice 1 per class For Extension or Demonstration supplies, see the corresponding section. ADVANCE PREPARATION Supplies Preparation Strawberries: Purchase fresh or thawed, green tops on or off.
    [Show full text]
  • Identification of Oxa1 Homologs Operating in the Eukaryotic
    Report Identification of Oxa1 Homologs Operating in the Eukaryotic Endoplasmic Reticulum Graphical Abstract Authors S. Andrei Anghel, Philip T. McGilvray, Ramanujan S. Hegde, Robert J. Keenan Correspondence [email protected] In Brief The absence of Oxa1/Alb3/YidC homologs in the eukaryotic endomembrane system has been a mystery. Now, Anghel et al. identify three ER-resident proteins, Get1, EMC3, and TMCO1, as remote homologs of Oxa1/ Alb3/YidC proteins and show that TMCO1 possesses YidC-like biochemical properties. This defines the ‘‘Oxa1 superfamily’’ of membrane protein biogenesis factors. Highlights d The ‘‘Oxa1 superfamily’’ comprises a group of membrane protein biogenesis factors d Three ER-resident proteins, Get1, EMC3, and TMCO1, are members of the superfamily d TMCO1, similar to bacterial YidC, associates with ribosomes and the Sec translocon Anghel et al., 2017, Cell Reports 21, 3708–3716 December 26, 2017 ª 2017 Elsevier Inc. https://doi.org/10.1016/j.celrep.2017.12.006 Cell Reports Report Identification of Oxa1 Homologs Operating in the Eukaryotic Endoplasmic Reticulum S. Andrei Anghel,1,2 Philip T. McGilvray,1 Ramanujan S. Hegde,3 and Robert J. Keenan1,4,* 1Department of Biochemistry and Molecular Biology 2Cell and Molecular Biology Graduate Program The University of Chicago, 929 East 57th Street, Chicago, IL 60637, USA 3MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK 4Lead Contact *Correspondence: [email protected] https://doi.org/10.1016/j.celrep.2017.12.006 SUMMARY proteins are inserted into the ER membrane by the WRB-CAML complex (Get1-Get2 in yeast; Mariappan et al., 2011; Schuldiner Members of the evolutionarily conserved Oxa1/Alb3/ et al., 2008; Vilardi et al., 2011; Wang et al., 2011, 2014; Yamamoto YidC family mediate membrane protein biogenesis at and Sakisaka, 2012).
    [Show full text]
  • Cellular Biology 1
    Cellular biology 1 INTRODUCTION • Specialized intracellular membrane-bound organelles (Fig. 1.2), such as mitochondria, Golgi apparatus, endoplasmic reticulum (ER). This chapter is an overview of eukaryotic cells, addressing • Large size (relative to prokaryotic cells). their intracellular organelles and structural components. A basic appreciation of cellular structure and function is important for an understanding of the following chapters’ information concerning metabolism and nutrition. For fur- ther detailed information in this subject area, please refer to EUKARYOTIC ORGANELLES a reference textbook. Nucleus The eukaryotic cell The nucleus is surrounded by a double membrane (nuclear Humans are multicellular eukaryotic organisms. All eukary- envelope). The envelope has multiple pores to allow tran- otic organisms are composed of eukaryotic cells. Eukaryotic sit of material between the nucleus and the cytoplasm. The cells (Fig. 1.1) are defined by the following features: nucleus contains the cell’s genetic material, DNA, organized • A membrane-limited nucleus (the key feature into linear structures known as chromosomes. As well as differentiating eukaryotic cells from prokaryotic cells) chromosomes, irregular zones of densely staining material that contains the cell’s genetic material. are also present. These are the nucleoli, which are responsible Inner nuclear Nucleus membrane Nucleolus Inner Outer Outer mitochondrial nuclear mitochondrial membrane membrane membrane Ribosome Intermembrane space Chromatin Mitochondrial Rough matrix Mitochondrial Nuclear endoplasmic ribosome pore reticulum Crista Mitochondrial mRNA Smooth Vesicle endoplasmic Mitochondrion Circular reticulum mitochondrial Proteins of the DNA Vesicle budding electron transport off rough ER Vesicles fusing system with trans face of Cytoplasm Golgi apparatus ‘Cis’ face + discharging protein/lipid Golgi apparatus ‘Trans’ face Lysosome Vesicles leaving Golgi with modified protein/lipid cargo Cell membrane Fig.
    [Show full text]
  • Introduction and Cell Membrane
    Introduction and Cell Membrane Peter Takizawa Department of Cell Biology Topics for today’s lecture • Course organization • Why cell biology • Cell membrane Cell Biology comprises a variety of activities that discuss basic science and disease. Lectures Website Cell Biology Clinical Histology Correlations Website !The Cell Biology course proper consists of three distinct activities: lectures, histology labs and clinical correlations. In addition, there are two electives that are associated with Cell Biology: molecular and cellular basis of disease and bench to bedside. Lectures will discuss the principles and concepts of modern cellular and molecular biology, focusing on the systems and mechanisms that allow cells to survive and perform specific functions in our bodies. The first part of the course will discuss the !systems and mechanisms that are common to most cells. The second part will discuss how the different types of cells in our bodies, utilize and modify those systems to perform specific biological functions. Histology examines the structure and functions of cells and how cells form tissues and organs. Histology places the cellular mechanisms presented in lecture into the context of cell and tissue structure. Histology also demonstrates how the !organization of cell and tissues allows organs to perform the physiological functions. Clinical correlations introduce students to clinical topics and medical terminology and demonstrate connections between basic science and disease. These presentations by physician-scientists, who are leaders in their fields, will sometimes include patients. You will notified when a patient is present. Why study cell biology to be a physician In order to understand how disease arises and how to treat disease, we need to learn how we work under normal conditions.
    [Show full text]
  • Cilia and Flagella: from Discovery to Disease Dylan J
    Dartmouth Undergraduate Journal of Science Volume 20 Article 2 Number 1 Assembly 2017 Cilia and Flagella: From Discovery to Disease Dylan J. Cahill Dylan Cahill, [email protected] Follow this and additional works at: https://digitalcommons.dartmouth.edu/dujs Part of the Engineering Commons, Life Sciences Commons, Medicine and Health Sciences Commons, Physical Sciences and Mathematics Commons, and the Social and Behavioral Sciences Commons Recommended Citation Cahill, Dylan J. (2017) "Cilia and Flagella: From Discovery to Disease," Dartmouth Undergraduate Journal of Science: Vol. 20 : No. 1 , Article 2. Available at: https://digitalcommons.dartmouth.edu/dujs/vol20/iss1/2 This Research Article is brought to you for free and open access by the Student-led Journals and Magazines at Dartmouth Digital Commons. It has been accepted for inclusion in Dartmouth Undergraduate Journal of Science by an authorized editor of Dartmouth Digital Commons. For more information, please contact [email protected]. BIOLOGY Cilia and Flagella: FromCilia and Discovery Flagella: to Disease From Discovery to Disease BY DYLAN CAHILL ‘18 Introduction certain insect sperm fagella (3, 5, 6). A unique Figure 1: Chlamydomonas intracellular transport mechanism known as reinhardtii, a single-celled, bi- In 1674, peering through the lens of a crude flagellate green alga, viewed intrafagellar transport is responsible for the light microscope, Antoni van Leeuwenhoek with a scanning electron assembly and maintenance of these organelles Chlamydomonas observed individual living cells for the frst time microscope. is (3, 6). Cilia and fagella are primarily composed a model organism in flagellar in history (1). He noted long, thin appendages of the protein tubulin, which polymerizes into dynamics and motility studies.
    [Show full text]
  • Cell Structure and Function in the Bacteria and Archaea
    4 Chapter Preview and Key Concepts 4.1 1.1 DiversityThe Beginnings among theof Microbiology Bacteria and Archaea 1.1. •The BacteriaThe are discovery classified of microorganismsinto several Cell Structure wasmajor dependent phyla. on observations made with 2. theThe microscope Archaea are currently classified into two 2. •major phyla.The emergence of experimental 4.2 Cellscience Shapes provided and Arrangements a means to test long held and Function beliefs and resolve controversies 3. Many bacterial cells have a rod, spherical, or 3. MicroInquiryspiral shape and1: Experimentation are organized into and a specific Scientificellular c arrangement. Inquiry in the Bacteria 4.31.2 AnMicroorganisms Overview to Bacterialand Disease and Transmission Archaeal 4.Cell • StructureEarly epidemiology studies suggested how diseases could be spread and 4. Bacterial and archaeal cells are organized at be controlled the cellular and molecular levels. 5. • Resistance to a disease can come and Archaea 4.4 External Cell Structures from exposure to and recovery from a mild 5.form Pili allowof (or cells a very to attach similar) to surfacesdisease or other cells. 1.3 The Classical Golden Age of Microbiology 6. Flagella provide motility. Our planet has always been in the “Age of Bacteria,” ever since the first 6. (1854-1914) 7. A glycocalyx protects against desiccation, fossils—bacteria of course—were entombed in rocks more than 3 billion 7. • The germ theory was based on the attaches cells to surfaces, and helps observations that different microorganisms years ago. On any possible, reasonable criterion, bacteria are—and always pathogens evade the immune system. have been—the dominant forms of life on Earth.
    [Show full text]