Serial dilution and colony counting ● Serial dilution and colony counting – Also know as “viable cell counts” – Concentrated samples are diluted by serial.

Slides:



Advertisements
Similar presentations
PHT 381 Lab # 6. Bacterial population count Many bacteriological studies require that we are able to determine the number of m.o per unit volume of a.
Advertisements

Bacterial Generation Time
140 micro Lab 8 : Counting of bacteria in Milk
ENUMERATION OF MICROORGANISMS
I. Microbial growth II. Environmental effects on microbial growth.
1 Microbial growth: prokaryotic cell cycle and growth curve Chapter 6.
PHT 381 Lab # 6. Bacterial population count Many bacteriological studies require that we are able to determine the number of m.o per unit volume of a.
Growth curves of micro-organisms. Learning Objectives  Discuss the growth curves of micro organisms  Outline the differences between batch and continuous.
Measurement of Bacterial Growth
Cell Growth Kinetics Introduction
Microbial Nutrition and Growth Microbial Population Growth
The Serial Dilution Method of Bacteria Enumeration
Bacterial Growth By Dr. Marwa Salah. Learning objectives Definition of bacterial growth. Requirements of bacterial growth. Types of respiration in bacteria.
Introduction to Lab Ex. 19: Enumeration of Bacteria
Chapter4 Microbial growth
Microbial Growth Growth in Batch Culture
Chapter 6: Microbial Growth
Growth and Cultivation of micro-organisms
Microbial growth: chapter 6
Inorganic Nutrient Availability & Phytoplankton Growth: the start of Biogeochemical Cycles Re-read pp , Habitat Determinants of Primary Production.
Microbial Growth and Culture
Culturing requirements
Microbial Growth 1.
Bacterial Growth Curve
Growth of bacteria in culture
Working with yeast Microbiologists have developed techniques for isolating and maintaining strains in the laboratory Strains: microorganisms of the same.
Bacterial growth:. Bacterial Growth Curve: The schematic growth curve shown below is associated with simplistic conditions known as a batch culture. It.
Binary fission of bacteria. E.coli genome size: 4.6 x 10 6 nucleotides Generation time at optimal conditions: 20min DNA replication rate: 1000nt/s ≈ 1.2.
Typically refers to an increase in population rather than in size
General Microbiology Laboratory Bacterial Generation Time.
Lecture 4 Dr. Dalia M. Mohsen Prof. of Microbiology.
Introduction Many studies require the quantitative determination of bacterial populations. The two most widely used methods for determining bacterial.
ABE 572 Bioprocess Engineering Lecture 1: Cell Growth.
Introduction to Bacteriology
Dr Rita Oladele Dept of Med Micro &Para CMUL/LUTH
Bacterial growth The mathematics of bacterial growth is fairly simple, since each original cell divides to form two new cells, with the loss of the original.
Microbial Growth. Growth of Microbes Increase in number of cells, not cell size One cell becomes colony of millions of cells.
 Many studies require the quantitative determination of bacterial populations. The two most widely used methods for determining bacterial numbers are:
Enumeration (determine the numbers of bacteria in a sample) Direct Measurement of Microbial Growth  Microscopic count - the microbes in a measured volume.
Microbial kinetics of growth and substrate utilization. Batch culture and Kinetics of Microbial growth in batch culture After inoculation the growth rate.
Microbial Growth refers to increase in number of cells not in size.
Microbial Growth.
Bacterial Growth November 2013.
Microbial Kinetics and Substrate utilization in Fermentation
Microbial Growth Growth in Batch Culture
Growth of Bacterial Culture
M ICROBIAL G ROWTH AND E NUMERATION. O BTAINING P URE C ULTURES  Pure Culture: Contains a single microbial species.  Most clinical and environmental.
Batch and Continuous Flow
BACTERIAL GROWTH CURVE MONOD’S EQUATION MADE BY JITENDRA PRATAP SINGH M TECH ENV ENGG.
PHT 381 Lab # 6 Bacterial population count.
Bacteria Cell Culture and Reproduction
BACTERIAL GROWTH & REPRODUCTION
Microbial Growth.
Growth of bacteria Dr. Sahar Mahdi.
Starter Decide whether the following statements relate to optical methods or dilution plating: Takes a very long time Uses a colorimeter Requires very.
MICROBIAL GROWTH AND REQUIREMENTS
Growth curves of micro-organisms
MICROBIAL GROWTH AND REQUIREMENTS
MICROBIAL GROWTH CURVE
Growth of bacteria Dr. Sahar Mahdi.
Microorganisms & Biotechnology
Learning Objectives i Understand the basic aseptic techniques used in culturing organisms. ii Understand the principles and techniques involved in culturing.
النمو والعد البكتيري Microbial growth النمو الجرثومي.
Bioreactors Engineering
Introduction Many studies require the quantitative determination of bacterial populations. The two most widely used methods for determining bacterial.
Metode Manual (Bergeys manual of bacteriology) sni.
Metabolism and Survival
Growth curves of micro-organisms
Bacterial Generation Time
Hadeel Kareem Musafer PhD
Presentation transcript:

Serial dilution and colony counting ● Serial dilution and colony counting – Also know as “viable cell counts” – Concentrated samples are diluted by serial dilution – The diluted samples can be either plated by spread plating or by pour plating

Serial dilution and colony counting ● Serial dilution (cont.) – Diluted samples are spread onto media in petri dishes and incubated – Colonies are counted. The concentration of bacteria in the original sample is calculated (from plates with 25 – 250 colonies, from the FDA Bacteriological Analytical Manual. – A simple calculation, with a single plate falling into the statistically valid range, is given below:

Serial dilution and colony counting Count the number of colonies on a plate that has between 25 and 250 colonies. Any plate which has more than 250 colonies is designated as "too numerous to count" (TNTC). Also any plate which has fewer than 25 colonies is designated as "too few to count" (TFTC). Notes: According to FDA Bacteriological Analytical Manual ( in rare situations) If there is no colony plate, use plate having nearest to 25 or 250 colonies. If all plates from a sample show no colonies, record count as 0.

Bacterial Generation time

Growth in Batch Culture “Growth” is generally used to refer to the acquisition of biomass leading to cell division, or reproduction. Growth is an increase in the number of cells, not an increase in size. A “batch culture” is a closed system in broth medium in which no additional nutrient is added after inoculation of the broth. Generation time: Generation time: time it takes for a cell to divide and the population to double.

Growth in Batch Culture ● Typically, a batch culture passes through four distinct stages: – Lag stage – Logarithmic (exponential) growth – Stationary stage – Death stage

Standard Bacterial Growth Curve in Batch Culture

Lag stage ( phase ) ● During lag phase, bacteria adapt themselves to growth conditions. ● It is the period where the individual bacteria are maturing and not yet able to divide. ● During the lag phase of the bacterial growth cycle, synthesis of RNA, enzymes and other molecules occurs. ● So in this phase the microorganisms are not dormant.

Logarithmic (exponential) growth ● Is a period characterized by cell doubling. ● This period in which the organisms are growing at the maximal rate possible. ● Generation time can be easily obtained from the exponential phase of a growth curve. ● Exponential growth cannot continue indefinitely, because the medium is soon depleted of nutrients and enriched with wastes.

Stationary stage (phase) ● Stationary phase, the growth rate slows as a result of nutrient depletion and accumulation of toxic products. ● This phase is reached as the bacteria begin to exhaust the resources that are available to them. ● This phase is a constant value as the rate of bacterial growth is equal to the rate of bacterial death.

Death stage (phase) ● The number of deaths eventually exceeds the number of new formed. ● Cell death may result from nutrient limitation, Toxic waste accumulation, loss of cell's ability to detoxify toxins and O 2 depletion.

Standard Bacterial Growth Curve in Batch Culture

Optical density is directly proportional to the number of cells. When the bacterial population doubles, the optical density of the bacterial suspension also doubles.