Lab 7 Goals and Objectives: Read the results: Gather all plates and tubes so we can discuss results together: ***Do NOT shake the FTM tubes!!!*** Your.

Slides:



Advertisements
Similar presentations
Week 10W New This Week: Last week: Gram (+) Bacteria ID
Advertisements

Shigella spp Isolation and Serotyping
General Microbiology Laboratory Bacteria Oxygen Requirements.
Materials: Each pair needs (for controls and unknowns): 5 glucose broths (red cap, red liquid, durham tube) 4 lactose broths (white cap, red liquid, durham.
الجامعة الإسلامية - غزة كلية العلوم قسم التحاليل الطبية الجامعة الإسلامية - غزة كلية العلوم قسم التحاليل الطبية Bacterial Oxygen Requirement By / Shadi.
Microbial Growth For microorganisms, growth is measured by increase in cell number, due to their limited increase in cell size.
Micro labs - review BIOL260 Winter Ubiquity What organisms grow best at room temperature? ___°C? At body temperature? = ___°C? What kind of medium.
Lab 14 Goals and Objectives: Exercise 69: Staphylococci Identification Read and record results Exercise 70: Streptococci & Enterococci Identification Read.
Exercise 18: Motility Determination
Chapter 6, part A Microbial Growth.
Microbiology Practical I The following slides were contributed by your fellow BIO 251 students… Use side “  ” key to view slides…
ASEPTIC TECHNIQUE Removing inoculum from a broth culture
1 How do you study something that you cant see? You look at it under the microscope –But certain microbes (e.g. bacteria) do not have too many identifying.
Copyright © 2004 Pearson Education, Inc., publishing as Benjamin Cummings PowerPoint ® Lecture Slide Presentation prepared by Christine L. Case Microbiology.
Lab 8&9 Goals and Objectives : Exercise 37: Morphological Study of Unknown Bacterium Exercise 38: Cultural Characteristics Discuss observations of the.
Lab 6 Goals and Objectives: Exercise 18: Motility Determination – presence of flagella Exercise 27: Effect of Oxygen on Growth Exercise 37: Morphological.
ASEPTIC TECHNIQUE Removing inoculum from a broth culture
Exercise 41: Multiple Test Media: Read and record results
Microbiology Class Four Culture Characteristics. Day 4 Exp 2B, Isolation of pure cultures form SPD, Streak Plate Dilution, Technique. Procedure: page.
Bacteria oxygen requirements
Bacteria Growth in the laboratory (in vitro). Bacterial nutrition and the design of culture media Based on bacterial metabolism* Culture pH Culture oxidation-
Growing of microorganism
Ex. 7: Aseptic Technique – Inoculating Different Types of Media Key concepts: 1.Different types of bacterial cultures: broth, agar slant, and agar deep.
Media & Biochemical Tests
Isolation technique with aseptic techniques to cultivate bacteria
General Microbiology Laboratory Sterile Technique & Pure Culture Concept.
Chapter 6, part A Microbial Growth.
Lab 8 Goals and Objectives: Do not disrupt BHI broths: need to see surface growth. Do not shake FTM tubes Make all Gram stain smears from broth & plates.
Exp 1: Culture Transfer Techniques , with organisms
Class Three February 7-9 Culture Characteristics
Class Two Fall – Spring Semester. Exp 1: Culture Transfer Techniques, w/ organisms Materials: per table: cultures – broths for EC, SM,ML, and BS per person.
Exercise 41: Multiple Test Media: Read and record results
General Microbiology Laboratory Anaerobic Bacteria.
Components Preparation Inoculation
Diagnosis of Bacterial Infection Bacterial Cultivation
Microbiology / Lab. 8. o Culture (Growth) Media I.What is a medium (plural media)? II.What is culture medium? III.What is meant by Inoculation of Media?
Gather all plates and tubes so we can discuss results together:
Lab #4. Review of Lab #3 Oxygen requirements Obligate aerobes (B. subtilis) Obligate anaerobes (C. sporogenes) Facultative anaerobes (E. coli, K. pneumoniae,
General Microbiology Laboratory 1.  Among the many enzymes that bacteria may produce are exoenzymes (those that are excreted) used to degrade large polymers.
 Nutrients - C, H, O, N, S. P, K, Mg, Fe, Ca, Mn, and traces of Zn, Co, Cu, and Mo. These elements are found in the form of water, inorganic ions, small.
You’re never too old to streak!
Ubiquity of Microorganisms.  A collection of a single type of bacteria isolated and growing free from all other microbes. Mixed CulturePure Culture.
Bacterial identification plating streaking how to inoculate how to observe.
Lab #3. Review of Lab #2 Gram staining  record results on pg. 35 Gram positive – purple Gram negative – pink Bacillus subtilis – Escherichia coli – Klebsiella.
*5 I’s Inoculation – Implanting Microbes into or upon culture media.
Culturing microorganisms, types of culture media, and nutrition. “Bacteria, it’s the only culture I’ve got.” “Without pure cultures all you get is nonsense.
NAS Lecturer: Mr. M. Zivuku LECTURE 4 1 Objectives By the end of this unit, you should be able to ; Explain the cultivation of bacteria in terms of in.
culturing of microorganism
Exercise 9: Aseptic Technique: Check results
Exercise 39: Oxidation and Fermentation Tests
Exercise 38: Cultural Characteristics (Gelatin) put on ice!!!
Inoculation Incubation Isolation Inspection Identification 5/6/2018
Corneal Cultures & Smears
Culturing Bacteria Growth Media
Chapter 41 Culture Techniques
Sterile Technique & Pure Culture Concept
Exercise 39: Oxidation and Fermentation Tests
Chapter 6, part A Microbial Growth.
Exercise 18: Motility Determination Read results
Chapter 6, part A Microbial Growth.
Microbiology Practical I
Unknowns.
Lab
Biology and Biotechnology department
Macronutrients : C,H,N,O,P,S
Tools of the Laboratory Power Point #1: Culturing Microorganisms
Biology & biotechnology department
Chapter 6, part A Microbial Growth.
Culture media Pure culture techniques & Bacterial colony
Media.
Presentation transcript:

Lab 7 Goals and Objectives: Read the results: Gather all plates and tubes so we can discuss results together: ***Do NOT shake the FTM tubes!!!*** Your Unknowns: Exercises 37 and 38 Check plates, record appearance, check for contamination Check slants for growth and place in my “reserve” rack Make new inoculations for both unknowns from the plates

Motility Test Media Results Non-motileMotile Not Motile Discriminates motility (presence of flagella), ability to “swim” through media Results: organism growing only in line of inoculation = non-motile organism appears as haze beyond line of inoculation = motile

Oxygen requirements 1. Fluid Thioglycolate Medium (FTM) Results:growth only at top = obligate aerobe growth only at bottom = obligate anaerobe even growth throughout = aerotolerant heavy growth at top, lighter growth at bottom = facultative growth only in middle = microaerophile 2. Brewer’s Anaerobic Agar Results: growth on aerobic agar only = obligate aerobe growth on anaerobic agar only = obligate anaerobe even growth on both = aerotolerant heavy growth on aerobic, lighter growth on anaerobic = facultative Fig 21.4 Fig 27.2

Which Groups Grow on Anaerobic Agar In the Anaerobic Jar? Which Groups Grow on Brewer’s in 20% Oxygen? Brewer’s No Oxygen Brewer’s 20% Oxygen Obligate aerobes: 20% O 2 Obligate anaerobes: O 2 toxic Facultative: w/ or w/o, better with O 2 Microaerophiles: 5-10% O 2 Aerotolerant: ignore O 2

Obligate aerobes: 20% O 2 Obligate anaerobes: O 2 toxic Facultative: w/ or w/o, better with O 2 Microaerophiles: 5-10% O 2 Aerotolerant: ignore O 2 Fig 27.1 Fig 27.5

Your Unknowns: Exercises 37 and 38 Check plates, record appearance, check for contamination Check slants for growth and place in my “reserve” rack Make new inoculations for both unknowns from the plates: 1.2 FTM tubes for O 2 requirements (Ex. 38 pg. 267) **leave caps loose to incubate! 2.2 BHI broth tubes for growth in liquid characteristics (Ex. 38 pg. 266 fig. 38.2) and for Gram stain (Ex. 37 pg. 260) 3.2 Gelatin stab cultures for gelatin hydrolysis ability (Ex. 38 pg. 259) 4.3 BHI plates each unknown (6 total), streak for isolation, to grow at 25°C, 30°C, 37°C to determine optimal temp. (Ex. 37&38 had you using slants and broths; side by side plates is easier) 5.2 Motility test media stabs (Ex. 37 pg. 262) No: KOH, endospore, acid fast, other structures (Ex. 37 pg )

Nutrient Gelatin Stab Inoculation method: stab with needle Contains: beef extract, peptone, high gelatin concentration to gel (no agar) Must be set on ice 5-10 min before reading Discriminates organisms that can produce gelatinases to hydrolyze the gelatin into amino acids Results: liquid = gelatin hydrolysis, positive for gelatinase production solid = negative for gelatinase production

Data to collect for Exercise 37 & 38 For Next Lab Gram result, size, shape, arrangement Transfer to Data Chart Motility Transfer to Data Chart Amount of growth Color Opacity Form Surface (broth) Subsurface (broth) Sediment (broth) Growth (broth) Temperature Transfer to Data Chart Oxygen requirements (FTM) Transfer to Data Chart Gelatin Transfer to Data Chart Colonies

Identification of Unknown Bacterium

For next lab: Read over formal lab report directions in packet. State a hypothesis “If the collective results of a profile of key biochemical assays are compared to the known results for limited subset of bacterial species, then a specific unknown culture from that subset of bacterial species can be correctly identified based on the results obtained from the biochemical assays.”

Each pair needs for Lab 7 4 motility stabs 4 FTM tubes 4 gelatin stab 4 BHI broths 12 BHIA plates