II. BACTERIAL GROWTH AND MICROBIAL METABOLISM
A. Bacterial Growth
Fundamental statements for this learning object:
1. Bacteria replicate by binary fission, a process by which one bacterium splits into two.
2. Generation time is the time it takes for a population of bacteria to double in number. For many bacteria the generation time ranges from minutes to hours.
3. Because of binary fission, bacteria increase their numbers by geometric progression whereby their population doubles every generation time.
4. Par proteins function to separate bacterial chromosomes to opposite poles of the cell during bacterial cell division.
5. The bacterial divisome is responsible for directing the synthesis of new cytoplasmic membrane and new peptidoglycan to form the division septum.
6. Although bacteria are capable of replicating geometrically as a result of binary fission, this only occurs as long as their is space to grow, sufficient nutrients, and a way to dispose of waste products.
7. In a closed growth system, a bacterial population usually exhibits a predictable pattern of growth - its growth curve - that follows several stages or phases.
8. During the lag phase growth is relatively flat and the population appears either not to be growing or growing quite slowly as newly inoculated cells are adapt to their new environment.
9. During the exponential growth phase (log phase) the population increases geometrically as long as there is sufficient food and space for growth.
10. During the stationary phase the population grows slowly or stops growing because of decreasing food, increasing waste, and lack of space.
11. During the death (decline) phase the population dies exponentially from the accumulation of waste products .
Bacterial Growth
Bacteria replicate by binary fission (def), a process by which one bacterium splits into two. Therefore, bacteria increase their numbers by geometric progression (def) whereby their population doubles every generation time.
Generation time (def) is the time it takes for a population of bacteria to double in number. For many common bacteria, the generation time is quite short, 20-60 minutes under optimum conditions. For most common pathogens in the body, the generation time is probably closer to 5-10 hours. Because bacteria grow by geometric progression and most have a short generation time, they can astronomically increase their number in a short period of time.
The relationship between the number of bacteria in a population at a given time (Nt), the original number of bacterial cells in the population (No), and the number of divisions those bacteria have undergone during that time (n) can be expressed by the following equation:
Nt = No X 2n
For example, Escherichia coli, under optimum conditions, has a generation time of 20 minutes. If one started with only 10 E. coli (No = 10) and allowed them to grow for 12 hours (n = 36; with a generation time of 20 minutes they would divide 3 times in one hour and 36 times in 12 hours), then plugging the numbers in the formula, the number of bacteria after 12 hours (Nt) would be
10 X 236 = Nt = 687,194,767,360 E. coli
In general it is thought that during DNA replication (discussed in Unit 6), each strand of the replicating bacterial DNA attaches to proteins at what will become the cell division plane. For example, Par proteins function to separate bacterial chromosomes to opposite poles of the cell during cell division. They bind to the origin of replication of the DNA and physically pull or push the chromosomes apart, similar to the mitotic apparatus of eukaryotic cells.
In the center of the bacterium, a group of proteins called Fts (filamentous temperature sensitive) proteins interact to form a ring at the cell division plane. These proteins form the cell division apparatus known as the divisome and are directly involved in bacterial cell division by binary fission (see Fig. 1 and Fig. 2).
The divisome is responsible for directing the synthesis of new cytoplasmic membrane and new peptidoglycan to form the division septum. The function of a number of divisome proteins have been identified, including:
- Scanning electron micrograph of dividing Escherichia coli; courtesy of CDC.
- Scanning electron micrograph of dividing Salmonella typhimurium; courtesy of CDC.
The Population Growth Curve
Although bacteria are capable of replicating geometrically as a result of binary fission, in reality this only occurs as long as their is space to grow, sufficient nutrients, and a way to dispose of waste products. Because these factors limit the ability to replicate geometrically, over time in a closed growth system a bacterial population usually exhibits a predictable pattern of growth - its growth curve - that follows several stages or phases:
1. The lag phase
During the lag phase growth is relatively flat and the population appears either not to be growing or growing quite slowly (see Fig. 3). During this phase the newly inoculated cells are adapting to their new environment and synthesizing the molecules they will need in order to grow rapidly.
2. The exponential growth phase (also called the logarithmic or log phase)
This is the phase where the population increases geometrically as long as there is sufficient food and space for growth (see Fig. 3).
3. The stationary growth phase
Here the population grows slowly or stops growing (see Fig. 3) because of decreasing food, increasing waste, and lack of space. The rate of replication is balanced out by the rate of inhibition or death.
4. The decline or death phase
Here the population dies exponentially from the accumulation of waste products (see Fig. 3), although the rate of death depends on the degree of toxicity and the resistance of the species and viable cells may remain for weeks to months.
Gary E. Kaiser, Ph.D.
Professor of Microbiology
The Community College of Baltimore County, Catonsville Campus
This work is licensed under a Creative Commons Attribution 4.0 International License.
Based on a work The Grapes of Staph at https://cwoer.ccbcmd.edu/science/microbiology/index_gos.html.
Last updated: Feb., 2020
Please send comments and inquiries to Dr.
Gary Kaiser