Chapter 5 - PPT Flashcards
(34 cards)
Binary fission:
cell division following enlargement of a cell to twice its minimum size 1 becomes 2, which becomes 4, which becomes 8, … Exponential; Logarithmic scale
Doubling time
time required for microbial cells to double in number A.k.a. generation time E. coli: short doubling time, 20 min B. japonicum: long doubling time, 24 hours Function of the slope of the line of cells vs. time on log scale Chapter 5 II
Divisome:
cell division apparatus FtsZ: forms ring around center of cel Fts (filamentous temperature-sensitive) proteins Essential for cell division in ZipA: anchor that connects FtsZ ring to cytoplasmic membrane FtsA: helps connect FtsZ ring to membrane and also recruits other divisome proteins
Divisome complex and FtsZ ring Image


Wall band and growth zone of Petidoglycan covered Cell
Exponential growth:
growth of a microbial population in which cell numbers double within a specific time interval (doubling time)
When graphed on linear scale – curved line
When graphed on logarithmic scale – straight line
Slope of line indicates doubling time
Doubling time graphs
Logorithmic and arathmatic

Doubling time
(dt) of the exponentially growing population is
dt = t/n
t is the duration of exponential growth
n is the number of generations during the period of exponential growth
Growth Rate
(v) is calculated as
v = 1/dt
Graphs of Exponential growth
Mathamatics and graphs

Batch Culture
a closed-system microbial culture of fixed volume
Lag phase
Exponential phase
Stationary phase
Death phase

Lag phase
Interval between when a culture is inoculated and when growth begins
Exponential phase
Cells in this phase are typically the healthiest
Primary metabolites produced
Stationary phase
Growth rate of population is zero
Either an essential nutrient is used up or product of the organism accumulated
Secondary metabolites are produced
Death Phase
If incubation continues after cells reach stationary phase, the cells will eventually die?
Continuous culture
an open-system microbial culture of fixed volume
Chemostat
: most common type of continuous culture device
Extend exponential phase, prevent stationary/death
Both growth rate and population density of culture can be controlled independently and simultaneously
Dilution rate: rate at which fresh medium is pumped in and spent medium is pumped out

Chemostat Graph

Microscopic Counts

Viable cell counts
(plate counts): measurement of living, reproducing population
Two main ways to perform plate counts:
Spread-plate method
Pour-plate method
To obtain the appropriate colony number, the sample to be counted should always be diluted
The Great Plate Anomaly
evaluation of natural samples reveal far more organisms than those recoverable on/in media
Microscopic methods count dead cells whereas viable methods do not
Different organisms have vastly different requirements for growth
Media biased towards certain microbes
Majority of microorganisms are viable, but not culturable
Dormant state
Scout hypothesis
Turbidity
(cloudiness) measurements are an indirect, rapid, and useful method of measuring microbial growth
Most often measured with a spectrophotometer
Measurement referred to as optical density (O.D.)
Spectrophotometer


