PowerPoint 5 - Microbial Growth
Introduction to Microbial Growth
Source of Content: Modified PowerPoint for BIO 275 (CVCC)
Textbook and resources available at OpenStax
Microbial Growth Basics
Definition: Microbial growth refers to the increase in the number of bacterial cells, not the size of individual microorganisms.
Colony Formation:
Starts from a single mother cell.
Cell division occurs via binary fission, creating offspring that form visible colonies in favorable conditions.
Binary Fission Process
Mechanism of Cell Division:
Common in bacteria, binary fission is a form of asexual reproduction.
The cell grows and duplicates its cellular components before dividing.
DNA Replication:
Begins at the origin of replication on the circular chromosome, attached to the inner cell membrane.
Continues until reaching the terminus, leading to the formation of new daughter cells through cytokinesis.
Visual Representation:
Electron micrographs depict the process and stages of binary fission in bacteria like Salmonella typhimurium.
Cytokinesis and FtsZ Action
Role of FtsZ Protein:
A key protein (similar to tubulin in eukaryotic cells) directs cytokinesis.
It assembles a Z ring on the cytoplasmic membrane, defining the division plane between daughter cells.
Divisome Formation:
Additional proteins join the Z ring to form the divisome, initiating new cell wall synthesis and septum formation.
Doubling Time and Generation Time
Definition: Time for a bacterial population to double through one round of binary fission.
Escherichia coli: Optimal doubling time of about 20 minutes, which may extend to several days under harsh conditions.
Generation Figures:
A single cell increases to over 1 million in 20 generations (~7 hours).
Example: Mycobacterium leprae doubling time is 14 days.
Microbial Growth Curve
Growth Curve Phases:
Lag Phase: Initial phase, characterized by cell adjustment and preparation for division.
Log Phase: Rapid exponential growth and division; cells are most metabolically active and susceptible to antibiotics.
Stationary Phase: Balance between cell division and death, reaching carrying capacity.
Death Phase: Increased waste and nutrient depletion lead to cell death; persister cells may survive.
Measuring Microbial Growth
Methods:
Plate Count: Viable cells counted based on visible colonies, expressed in CFUs.
Serial Dilution: Helps achieve manageable counts within accurate statistical ranges for microbial estimates.
Filtration Method: Used for low bacterial counts in samples like water to detect coliforms.
Coulter Counter: Counts cells as they pass through a detector in a liquid sample.
Biofilms and Their Importance
Characteristics:
Structured microbial communities that thrive on surfaces, secreting extracellular polymeric substances (EPS) to form a protective matrix.
Quorum Sensing:
Communication between cells in biofilms using signaling molecules to coordinate responses based on population density.
Clinical Relevance:
Biofilms can enhance resistance to antibiotics and contribute to chronic infections.
Environmental Conditions Affecting Microbial Growth
Anaerobic Environments: Locations like bogs or the rumen provide oxygen-free conditions favorable for specific bacteria.
pH and Temperature Tolerance:
Microbes have specific ranges required for optimal growth (e.g. neutrophiles near pH 7, thermophiles thrive at high temperatures).
Salt Concentration: Halophiles adapt to high salinity environments, such as those found in salt lakes.
Culture Media in Microbiology
Types of Media:
Agar: The most common solidifying agent, solidifies at temperatures below 40°C.
Selective and Differential Media: Used to isolate specific microbes or distinguish between different species based on color change.
Examples:
MacConkey agar differentiates lactose fermenters (e.g., E. coli) from non-fermenters.
Blood agar identifies hemolytic bacteria like Listeria.