Introduction to Biotechnology: a Georgia Teachers Resource Manual
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Career Guide Biological Sciences Concentration in Microbiology
MAJOR TO BACHELOR OF SCIENCE IN CAREER GUIDE BIOLOGICAL SCIENCES CONCENTRATION IN MICROBIOLOGY Majoring in biological sciences with a concentration in microbiology provides students with intellectual and technical skills required for success in the broad area of microbiology, which includes clinical, environmental, ecological, evolutionary, molecular, metabolic, and physiological perspectives of microbes, including aspects of virology and immunology. Students concentrating in microbiology should also be able to explain the diversity and ABOUT THE MAJOR/ similarity of microbes, including their physiology, mechanisms of pathogenesis and host CONCENTRATION defenses, and unique ecology. SKILLS Research Problem-Solving Ability to Operate Critical Thinking Scientific Equipment Agricultural and Food Scientist Environmental Scientist Quality Control Analyst Bacteriologist Lab Technician* Regulatory Affairs Specialist Biomedical Scientist* Medical Device Specialist Research Microbiologist Biotechnologist* Mycologist Science Educator* Cell Biologist Parasitologists Virologist POTENTIAL CAREER Clinical Microbiologist Public Health Professional OPPORTUNITIES *Additional education/certification may be required COMMON CAREER AREAS FOR THIS MAJOR Organismal/ Research & Biomedical Healthcare Ecological Education Biotechnology Bioinformatics Development Sciences Biology Do volunteer work Get part-time job or internship Did you know UNLV has programs, student A part-time, temporary, and summer job or groups, and academic service-learning internship can -
An Instrumented Centrifuge for Studying Mouse Locomotion and Behaviour Under Hypergravity Benjamin J
© 2019. Published by The Company of Biologists Ltd | Biology Open (2019) 8, bio043018. doi:10.1242/bio.043018 METHODS AND TECHNIQUES An instrumented centrifuge for studying mouse locomotion and behaviour under hypergravity Benjamin J. H. Smith* and James R. Usherwood ABSTRACT (Alexander, 1984). Investigating the limitations of inverted Gravity may influence multiple aspects of legged locomotion, from the pendulum models of locomotion may lead to advances in robotics periods of limbs moving as pendulums to the muscle forces required and treatment of gait pathologies, as well as our fundamental to support the body. We present a system for exposing mice to understanding of legged locomotion. hypergravity using a centrifuge and studying their locomotion and The motion of an inverted pendulum can be described using u€ ¼ g u u€ activity during exposure. Centrifuge-induced hypergravity has the the equation L sin , where is angular acceleration, g is θ advantages that it both allows animals to move freely, and it affects gravitational acceleration, L is length, and is angular displacement both body and limbs. The centrifuge can impose two levels of from the equilibrium point; testing the predictions of inverted hypergravity concurrently, using two sets of arms of different lengths, pendulum-based models therefore requires the manipulation of either each carrying a mouse cage outfitted with a force and speed L or g. Differences in L are usually studied by comparing similar measuring exercise wheel and an infrared high-speed camera; both animals of different sizes (Gatesy and Biewener, 1991; Daley and triggered automatically when a mouse begins running on the wheel. -
THE CASE for FIRST AMENDMENT PROTECTION of BIOART in 2000
FREEDOM TO EXPRESS A BIOLOGICAL CONSTRUCT: THE CASE FOR FIRST AMENDMENT PROTECTION OF BIOART KEITH SYVERSON INTRODUCTION In 2000, contemporary artist Eduardo Kac made international headlines by partnering with scientists at the Institut National de la Recherche Agronomique (INRA), France where together they genetically engineered an albino rabbit to express an enhanced green fluorescent protein (GFP)1 so that the rabbit would glow green when exposed to blue light.2 The entire project from its conception to the final display was intended as an artistic experiment to challenge society’s views on animal experimentation and the selective breeding of pets.3 This type of work that merges art and biology is called “BioArt.” According to Eduardo Kac, BioArt “employs one or more of the following approaches: (1) the coaching of biomaterials into specific inert shapes or behaviors; (2) the unusual or subversive use of biotech tools and processes; (3) the invention or transformation of living organisms with or without social environmental integration."4 BioArt has arguably existed for centuries.5 For example, some commentators have described the primitive methods of brewing beer in the Old Kingdom as form of BioArt.6 Similarly, the artificial selection involved in agriculture has been viewed by some as a form of 1 Frances Stracey, Bio-art: The Ethics Behind the Aesthetics, 10 NATURE REVIEWS: MOLECULAR CELL BIOLOGY 496, 499 (2009). 2 Id. 3 Id. 4 Eduardo Kac, Art That Looks You in the Eye: Hybrids, Clones, Mutants, Synthetics, and Transgenics, in SIGNS OF LIFE 1, 18 (Eduardo Kac ed., MIT Press, 2007). 5 See Edgar DaSilva, Art, Biotechnology and the Culture of Peace, 7 ELECTRONIC JOURNAL OF BIOTECHNOLOGY 130, 131-32 (2004) (arguing that the brewing reliefs in Egypt during the Old Kingdom from 2650 BC are an example of BioArt). -
PHYSICS of ARTIFICIAL GRAVITY Angie Bukley1, William Paloski,2 and Gilles Clément1,3
Chapter 2 PHYSICS OF ARTIFICIAL GRAVITY Angie Bukley1, William Paloski,2 and Gilles Clément1,3 1 Ohio University, Athens, Ohio, USA 2 NASA Johnson Space Center, Houston, Texas, USA 3 Centre National de la Recherche Scientifique, Toulouse, France This chapter discusses potential technologies for achieving artificial gravity in a space vehicle. We begin with a series of definitions and a general description of the rotational dynamics behind the forces ultimately exerted on the human body during centrifugation, such as gravity level, gravity gradient, and Coriolis force. Human factors considerations and comfort limits associated with a rotating environment are then discussed. Finally, engineering options for designing space vehicles with artificial gravity are presented. Figure 2-01. Artist's concept of one of NASA early (1962) concepts for a manned space station with artificial gravity: a self- inflating 22-m-diameter rotating hexagon. Photo courtesy of NASA. 1 ARTIFICIAL GRAVITY: WHAT IS IT? 1.1 Definition Artificial gravity is defined in this book as the simulation of gravitational forces aboard a space vehicle in free fall (in orbit) or in transit to another planet. Throughout this book, the term artificial gravity is reserved for a spinning spacecraft or a centrifuge within the spacecraft such that a gravity-like force results. One should understand that artificial gravity is not gravity at all. Rather, it is an inertial force that is indistinguishable from normal gravity experience on Earth in terms of its action on any mass. A centrifugal force proportional to the mass that is being accelerated centripetally in a rotating device is experienced rather than a gravitational pull. -
Biotechnology: Answers to Common Questions
FSR0030 Biotechnology: Answers to Common Questions Kevin Keener, Assistant Professor of Food Science Thomas Hoban, Professor of Sociology and Food Science N.C. Cooperative Extension Service N.C. State University We are entering the “Century of Biology.” Recent developments in the biological sciences are giving us a better understanding of the natural world. At the same type we are developing new tools that are collectively referred to as “biotechnology.” These help us address problems related to human health, food production, and the environment. Any new technology – particularly one as far-reaching as biotechnology – will generate interest, as well as concerns. Because the science behind biotechnology is complex, misconceptions arise over its impacts and implications. In this publication we will answer questions many people have about biotechnology. These questions are organized along the lines of a news story: what, when, who, where, why, and how. We also provide a list of additional information sources available on the Internet. Our primary focus will be on the uses of biotechnology in agriculture and food production since these appear to be more controversial than other applications (at least up until this time). What is Biotechnology? In its broadest sense, biotechnology refers to the use of living systems to develop products. New scientific discoveries are allowing us to better understand fundamental life processes at the cellular and molecular level. Now we can improve selected attributes of microbes, plants, or animals for human use by making precise genetic changes that were not possible with traditional methods. All living organisms contain genes that carry the hereditary traits between generations. -
Laboratory Exercises in Microbiology: Discovering the Unseen World Through Hands-On Investigation
City University of New York (CUNY) CUNY Academic Works Open Educational Resources Queensborough Community College 2016 Laboratory Exercises in Microbiology: Discovering the Unseen World Through Hands-On Investigation Joan Petersen CUNY Queensborough Community College Susan McLaughlin CUNY Queensborough Community College How does access to this work benefit ou?y Let us know! More information about this work at: https://academicworks.cuny.edu/qb_oers/16 Discover additional works at: https://academicworks.cuny.edu This work is made publicly available by the City University of New York (CUNY). Contact: [email protected] Laboratory Exercises in Microbiology: Discovering the Unseen World through Hands-On Investigation By Dr. Susan McLaughlin & Dr. Joan Petersen Queensborough Community College Laboratory Exercises in Microbiology: Discovering the Unseen World through Hands-On Investigation Table of Contents Preface………………………………………………………………………………………i Acknowledgments…………………………………………………………………………..ii Microbiology Lab Safety Instructions…………………………………………………...... iii Lab 1. Introduction to Microscopy and Diversity of Cell Types……………………......... 1 Lab 2. Introduction to Aseptic Techniques and Growth Media………………………...... 19 Lab 3. Preparation of Bacterial Smears and Introduction to Staining…………………...... 37 Lab 4. Acid fast and Endospore Staining……………………………………………......... 49 Lab 5. Metabolic Activities of Bacteria…………………………………………….…....... 59 Lab 6. Dichotomous Keys……………………………………………………………......... 77 Lab 7. The Effect of Physical Factors on Microbial Growth……………………………... 85 Lab 8. Chemical Control of Microbial Growth—Disinfectants and Antibiotics…………. 99 Lab 9. The Microbiology of Milk and Food………………………………………………. 111 Lab 10. The Eukaryotes………………………………………………………………........ 123 Lab 11. Clinical Microbiology I; Anaerobic pathogens; Vectors of Infectious Disease….. 141 Lab 12. Clinical Microbiology II—Immunology and the Biolog System………………… 153 Lab 13. Putting it all Together: Case Studies in Microbiology…………………………… 163 Appendix I. -
Continuous-Flow Centrifugation to Collect Suspended Sediment for Chemical Analysis
1 Table 6. Compounds detected in both equipment blank samples and not in corresponding source blank samples or at concentrations greater than two times the corresponding source blank sample concentration. Prepared in cooperation with the National Water Quality Monitoring Council and [Source data: Appendix A, table A1; Conn and Black (2014, table A4); and Conn and others (2015, table A11). CAS Registry Number: Chemical Abstracts Service Washington State Department of(CAS) Ecology Registry Number® (RN) is a registered trademark of the American Chemical Society. CAS recommends the verifi cation of CASRNs through CAS Client ServicesSM. Method: EPA, U.S. Environmental Protection Agency’s SW 846; SIM, select ion monitoring. Unit: µg/kg, microgram per kilogram; ng/kg, nanogram per kilogram. Sample type: River samples were from the Puyallup River, Washington. Q, qualifi er (blank cells indicate an unqualifi ed detection). J, estimated, result between the Continuous-Flow Centrifugationdetection level and reporting level; toNJ, result Collect did not meet all quantitation Suspended criteria (an estimated maxiumum possible concentration is reported in Result column) U, not detected above the reporting level (reported in the Result column); UJ, not detected above the detection level (reported in the Result column). Abbreviations: na, not Sediment for Chemicalapplicable; Analysis PCBs, polychlorinated biphenyls] Sample type Chapter 6 of CAS River River Commercial Commercial Section D, Water Quality Parameter name Registry Method Unit source equipment -
BIO-210 Introduction to Biotechnology
Bergen Community College Division of Mathematics, Science, and Technology Department of Biology and Horticulture Introduction to Biotechnology (BIO-210) General Course Syllabus Spring 2016 Course Title: BIO-210 Introduction to Biotechnology Course Description: This course is designed to give students both a theoretical background and a working knowledge of the instrumentation and techniques employed in a biotechnology laboratory. Emphasis will be placed on the introduction of foreign DNA into bacterial cells, as well as the analysis of nucleic acids (DNA and RNA) and proteins. Prerequisites: BIO-101 General Biology I General Education Course: No Course Credits 4.0 Hours per week: 6.0: 3 hours lecture and 3 hours lab Course Coordinator: John Smalley Required Textbook: Introduction To Biotechnology, 3rd edition, Thieman, W.J. and M.A. Palladino. Pearson/Benjamin Cummings. Required Lab Manual: None Student Learning Objectives The student will be able to: 1. Students will demonstrate proper scientific laboratory record keeping. Students will be evaluated by periodic notebook collections. 2 Students will be able to explain the scientificbasis for each technique used. Students will be required to answer exam questions designed to allow them to demonstrate their acquisition and retention of this knowledge. 3. Students will learn how to introduce foreign DNA into bacterial cells for the purpose of molecular cloning. Students will be evaluated by observation in the laboratory and analysis of experimental results. Assessment will also be based upon performance on exam questions. 4. Students will be able to retrieve cloned DNA and analyze it using restriction endonuclease digestion and agarose gel electrophoresis. Students will be evaluated by observation in the laboratory and analysis of experimental results. -
Gas Centrifuge Technology: Proliferation Concerns and International Safeguards Brian D
Gas Centrifuge Technology: Proliferation Concerns and International Safeguards Brian D. Boyer Los Alamos National Laboratory Trinity Section American Nuclear Society Santa Fe, NM November 7, 2014 Acknowledgment to M. Rosenthal (BNL), J.M. Whitaker (ORNL), H. Wood (UVA), O. Heinonen (Harvard Belfer School), B. Bush (IAEA-Ret.), C. Bathke (LANL) for sources of ideas, information, and knowledge UNCLASSIFIED Operated by Los Alamos National Security, LLC for the U.S. Department of Energy's NNSA Enrichment / Proliferation / Safeguards . Enrichment technology – The centrifuge story . Proliferation of technology – Global Networks . IAEA Safeguards – The NPT Bargain Enrichment Proliferation Safeguards U.S. DOE Centrifuges – DOE / Pres. George W. Bush at ORNL B. Boyer and K. Akilimali - IAEA Zippe Centrifuge – Deutsches Museum (Munich) briefed on seized Libyan nuclear Safeguards Verifying Spent Fuel in www.deutsches-museum.de/en/exhibitions/energy/energy-technology/nuclear-energy/ equipment (ORNL) Training in Sweden (Ski-1999) UNCLASSIFIED 2 Operated by Los Alamos National Security, LLC for the U.S. Department of Energy's NNSA The Nuclear Fuel Cycle and Proliferation Paths to WMDs IAEA Safeguards On URANIUM Path Weapon Assembly Convert UF6 to U Metal Pre-Safeguards Natural Enriched DIVERSION Material (INFCIRC/153) Uranium Uranium PATH “Open” Cycle WEAPONS PATHS Fuel – Natural Uranium or LEU In closed cycle – MOX Fuel (U and Pu) “Closed” Cycle IAEA Safeguards On PLUTONIUM Path Convert Pu Plutonium Compounds to Pu Metal DIVERSION PATH To Repository -
Basics in Centrifugation - Eppendorf Handling Solutions Page 1 of 5
Basics in Centrifugation - Eppendorf Handling Solutions Page 1 of 5 Menu • Home • Sample Handling • Centrifugation • Safe Use of Centrifuges • Basics in Centrifugation Basics in Centrifugation • Biosafety • Safe Use of Centrifuges • Centrifugation Applications • This and That • Braking Ramps • Thermal Conductivity • Centrifuge Maintenance • Ergonomics • share • tweet • share • mail Basics in Centrifugation Centrifugation is a technique that helps to separate mixtures by applying centrifugal force. A centrifuge is a device, generally driven by an electric motor, that puts an object, e.g., a rotor, in a rotational movement around a fixed axis. A centrifuge works by using the principle of sedimentation: Under the influence of gravitational force (g-force), substances separate according to their density. Different types of separation are known, including isopycnic, ultrafiltration, density gradient, phase separation, and pelleting. https://handling-solutions.eppendorf.com/sample-handling/centrifugation/safe-use-of-cent... 10/24/2018 Basics in Centrifugation - Eppendorf Handling Solutions Page 2 of 5 Pelleting is the most common application for centrifuges. Here, particles are concentrated as a pellet at the bottom of the centrifuge tube and separated from the remaining solution, called supernatant. During phase separation, chemicals are converted from a matrix or an aqueous medium to a solvent (for additional chemical or molecular biological analysis). In ultrafiltration, macromolecules are purified, separated, and concentrated by using a membrane. Isopycnic centrifugation is carried out using a "self- generating" density gradient established through equilibrium sedimentation. This method concentrates the analysis matches with those of the surrounding solution. Protocols for centrifugation typically specify the relative centrifugal force (rcf) and the degree of acceleration in multiples of g (g-force). -
Genetically Modified, Red Fluorescent Zebrafish: Detection, Crossing
Journal of Environmental Biotechnology Vol. 8, No. 2, 105–110, 2008 Original paper (regular paper) Genetically Modifi ed, Red Fluorescent Zebrafi sh: Detection, Crossing, Inheritance of Red Fluorescence, and Tolerance to Low Temperatures KIMIKO AMANUMA*, NOBUYOSHI NAKAJIMA, AKIKO H. HASHIMOTO and YASUNOBU AOKI National Institute for Environmental Studies, 16–2 Onogawa, Tsukuba, Ibaraki 305–8506, Japan * TEL: +81–(0)29–850–2390 FAX: +81–(0)29–850–2588 * E-mail: [email protected] (Received; 28 September, 2008/Accepted; 10 October, 2008) Under Cartagena Protocol domestic law, genetically modifi ed (GM) fi sh have not yet received permission to be imported or sold in Japan. However, it is anticipated that ornamental, fl uorescent GM fi sh will be imported and sold prior to any offi cial process for evaluating their eff ects on biological diversity as GM organisms (GMO). Therefore, we have devised a method for detecting GM fi sh that utilizes PCR for the detection of replication origins of plasmids that generally exist as transgenes integrated in the GMOs’ chromosomes. Using red fl uorescent zebrafi sh (rfZF), sold in Japan, and rpsL GM ZF established by us, we demonstrated the feasibility of this method for detecting GMO. Next, we examined the biological characteristics of the GM rfZF. They were able to cross with non-GM ZF; the red fl uorescence was inherited by their progeny according to expected outcomes, based on Mendelian genetics. Examination of the low temperature tolerance of rfZF and non-GM fi sh indicated that the lethal, minimum temperature was the same for both fi sh (5°C). -
Microbiology Mary Jane Ferraro and Robert C
Chapter Microbiology Mary Jane Ferraro and Robert C. Moellering Jr. he history of Microbiology (or Bacte- abrupt departure the following year, Dr. Law- Triology, as it was originally known) at the rence Kunz, who had come to the MGH as an Massachusetts General Hospital (MGH) is a Assistant Bacteriologist in 1952, assumed de facto complex one. Although Dr. Reginald Heber responsibility for the laboratory until he was offi - Fitz’s pioneering work established the pathogen- cially appointed chief in 1956. During his tenure esis of appendicitis in 1886 (15, 41; and see chapter the Department of Bacteriology developed close 2), the laboratory specialty of microbiology owes ties with the Infectious Diseases Division and the its origins to Dr. James Homer Wright, who was Department of Medicine. Th is was also a time appointed Pathologist at MGH in 1896. Wright during which a number of “boutique” clinical was involved in a number of landmark studies laboratories sprang up throughout the hospital. in the etiology of parasitic and other infections, Microbiology and Infectious Diseases were no established the fi rst diagnostic bacteriology labo- exception, and in rapid order independent labo- ratory functions at the MGH, and hired several ratories of Antibiotic Blood Levels, Parasitology, physicians to undertake bacteriological work in and Virology were established in the Infectious the department. In 1925, just before the end of Dr. Diseases Unit. All these had close relationships Wright’s tenure as chief, the offi cial position of with the Bacteriology Laboratory as well. In 1989 Bacteriologist was established in the Department the activities of the Bacteriology/Clinical Micro- of Pathology, and this was held in succession by biology Laboratory were once again returned to Drs.