Microbial Nutrition and Growth
Microbial Nutrition and Growth
Microorganisms have are certain physical and chemical requirements they must possess to survive, reproduce, and grow.
Microbiologists use the term growth to indicate an increase in a population of microbes rather than an increase in size. One of the reasons prokaryotic organisms, like bacteria, have been so successful for billions of years, is that they reproduce very quickly using a process called binary fission. Binary fission creates two genetically identical daughter cells from one single parent cell. This process is more simple than mitosis, which occurs in eukaryotic cells, and it requires less energy.
Most bacterial organisms reproduce by an asexual process called binary fission, which usually occurs after a period of growth in which the cell increases in size. The bacterial chromosome is replicated at the beginning of binary fission, resulting in 2 DNA molecules. The 2 chromosomes separate rather easily compared to cell division in eukaryotic cells. Bacterial cells do not require a mitotic spindle (or centrosome) to separate their replicated chromosomes, like eukaryotic cells do. Following chromosomal segregation, a septum is formed at the midline of the dividing cell. The septum continues to grow and eventually separates the dividing cell into two genetically identical daughter cells.
Generation (or Doubling)Time
Microorganisms reproduce rapidly using binary fission. Microbes will reproduce exponentially as long as they have the needed nutrients and space and have a habitat free of toxins. This means that a single microorganism can quickly generate a population of cells that are astronomical in number!
- Generation Time - This is the time required for a population of cells to double in size. Most bacteria have a generation time of 1-3 hours.
The interval of time between successive binary fissions of a cell or population of cells is known as the generation time (or doubling time).
Under optimal conditions, some species have a very fast generation time; for others, it is much slower. For example, the optimal generation time.
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If Escherichia coli were able to undergo consecutive rounds of binary fissions uninterrupted for only 36 hours, they would be able to cover the entire surface of the Earth!
So, WHY ARE WE NOT KNEE-DEEP IN E.COLI? E. Coli, like any other cell have needs! They require proper nutrition, they require certain environmental conditions, and perhaps... a little bit of love? Pathogenic microorganisms (microbes that cause disease) that have a shorter generation time, will produce symptoms more quickly in organisms that they have infected. The period of time that exists between exposure to the pathogen and the onset of symptoms is called the incubation period. In other words, we can say that the faster a microorganism reproduces, the shorter incubation period will be experienced for the disease cause by the microorganism.
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Most of us have had some form of food poisoning at some point in our lives. Some strains of E. coli (pathogen E. coli O157:H7) can cause food poisoning. If you were to ingest only one of these pathogenic cells with your under cooked breakfast at 8:00 AM, your body would have over 2 million E. coli cells by only 3:00 PM that afternoon!
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Growth of Microbial Populations
Phases of Microbial Growth
When we analyze bacterial growth, it is convenient to create a graph of the number of bacteria versus time. This type of graph is called a "growth curve". Analyzing these growth curves reveals distinct phases of bacterial growth.
- The Lag Phase - The lag phase of the growth curve is generated from the bacteria adjusting to their new environment. The cells will not undergo binary fission until they have adapted to the new habitat.
- The Log Phase - The log phase of the growth curve reveals the active growth of bacteria in the population.
- The Stationary Phase - When the population of bacteria begins to run out of space and nutrients and/or when toxins are built up in the culture, the log phase will give way to the stationary phase. In the stationary phase, the number of bacteria cells in the population will remain fairly consistent due to the fact that the number of cells being created will be roughly equal to the number of cells dying.
- The Death Phase - After some time, the depletion of nutrition and space and the buildup of toxins in the culture, will cause more cells to be dying than cell being produced. This is the death phase of the growth curve.
Endospores
Endospores are dormant structures that can endure times of environmental stress.
A few gram-positive bacterial species, such as the soil-dwelling bacteria of the genera Bacillus and Clostridium, produce endospores in times of stress.
When environmental conditions are good, bacterial cells grow, mature, and reproduce as vegetative cells. However, when condition for growth become strained, these bacteria are able to survive harsh conditions through spore formation or sporulation.
When environmental conditions are good, bacterial cells grow, mature, and reproduce as vegetative cells. However, when condition for growth become strained, these bacteria are able to survive harsh conditions through spore formation or sporulation.
Steps of Endospore Formation
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Microorganisms are everywhere; on our skin, on surfaces and in the air. Because this is the case, it is important to protect cell cultures from contamination. Microbiologists are usually intending to grow axenic cultures. An axenic culture will consist of a colony of cells generated from a single parent cell (progenitor cell) or colony-forming unit (CFU). In order to produce such a cell culture, efforts must be taken to sterilize any substance, media, loops, glassware, etc. that may come into contact with the culture. Sterile techniques have been developed to reduce the risk of contamination. Here are some of the more popular sterile techniques used today.
- The Streak Plate Method. In this technique, a sterile inoculating loop is used to spread an inoculum across the surface of the agar in a Petri dish. The dish or plate will develop colonies following a time of incubation.
- The Pour Plate Technique - In this technique, colonies are isolated through a series of serial dilutions. The final dilution is then added to warm agar in a Petri dish. The dish will produce colonies after an incubation period.