Chapter 9: Problem 6
Which of the following methods brings about cell lysis due to cavitation induced by rapid localized pressure changes? a. microwaving b. gamma irradiation c. ultraviolet radiation d. sonication
Short Answer
Expert verified
Sonication brings about cell lysis due to cavitation induced by rapid localized pressure changes.
Step by step solution
01
Understand cell lysis and cavitation
Cell lysis refers to the disruption or breaking down of the cell membrane, leading to the release of cellular contents. Cavitation is a process where rapid pressure changes create small vapor-filled cavities or bubbles in a liquid. When these bubbles collapse, they generate shock waves that can cause cell lysis.
02
Review the methods listed
Look at each provided option and understand how they work. Microwaving heats substances using microwave radiation. Gamma irradiation uses high-energy photons to ionize molecules, and UV radiation damages genetic material through high-energy photons. Sonication generates sound waves that produce cavitation.
03
Identify the method involving cavitation
Find the method among the options that causes cell lysis through cavitation. Only sonication relies on the generation of sound waves that can cause cavitation, leading to rapid localized pressure changes that induce cell lysis.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Cavitation in Microbiology
Cavitation is a phenomenon often mentioned in the context of fluid dynamics, but it also plays a significant role in microbiology. In microbial studies and biotechnological applications, cavitation refers to the formation of vapor cavities or 'microbubbles' within a liquid. When subjected to rapid changes in pressure, these microbubbles collapse and generate powerful shock waves.
For microbial cells, these shock waves can be sufficiently forceful to cause cell lysis, which is the disruption of the cell membrane and the subsequent release of cellular contents. Cell lysis is crucial for a variety of laboratory techniques, where extracting the contents of microbial cells, such as proteins, DNA, and other biomolecules, is necessary for further study or application.
The beauty of using cavitation for cell lysis lies in its efficiency and specificity. By carefully controlling the pressure variations, scientists can target very small volumes, ensuring that lysis occurs selectively and with limited collateral damage to the desired product or the surrounding environment.
For microbial cells, these shock waves can be sufficiently forceful to cause cell lysis, which is the disruption of the cell membrane and the subsequent release of cellular contents. Cell lysis is crucial for a variety of laboratory techniques, where extracting the contents of microbial cells, such as proteins, DNA, and other biomolecules, is necessary for further study or application.
The beauty of using cavitation for cell lysis lies in its efficiency and specificity. By carefully controlling the pressure variations, scientists can target very small volumes, ensuring that lysis occurs selectively and with limited collateral damage to the desired product or the surrounding environment.
Sonication Process
The sonication process is a powerful tool largely used in microbiology to disrupt cells through ultrasonic waves. During sonication, sound waves at frequencies typically beyond the range of human hearing (usually above 20 kHz) are introduced into a liquid medium. These waves create alternating high-pressure and low-pressure cycles in the liquid.
Under high pressure, microbubbles form, and as the cycle shifts to low pressure, these bubbles rapidly collapse—a process referred to as 'cavitation.' The cavitation generates intense shear forces and localized extremes of temperature and pressure. When microbial cells suspended in the liquid are exposed to these extreme conditions, their cellular membranes rupture, leading to lysis.
Sonication is especially valued for its ability to lyse cells in a controlled and reproducible manner, allowing for high recovery of intracellular components. It's also a relatively quick and non-chemical method, making it an environmentally friendly alternative to other cell disruption techniques that rely on detergents or solvents.
Under high pressure, microbubbles form, and as the cycle shifts to low pressure, these bubbles rapidly collapse—a process referred to as 'cavitation.' The cavitation generates intense shear forces and localized extremes of temperature and pressure. When microbial cells suspended in the liquid are exposed to these extreme conditions, their cellular membranes rupture, leading to lysis.
Sonication is especially valued for its ability to lyse cells in a controlled and reproducible manner, allowing for high recovery of intracellular components. It's also a relatively quick and non-chemical method, making it an environmentally friendly alternative to other cell disruption techniques that rely on detergents or solvents.
Microbial Cell Disruption Techniques
Cell disruption techniques are vital in microbiology and biotechnology to access the intracellular components of microbial cells. Various methods can be employed, depending on the type and sturdiness of the cell as well as the desired purity and intactness of the intracellular contents.
Some commonly used physical techniques include:
Each technique has its own merits and drawbacks, and often a combination of methods is used to achieve optimal cell disruption while preserving the integrity of the cellular components.
Some commonly used physical techniques include:
- Homogenization: This method uses shear force to break cells, typically through mechanical means such as grinding, stirring or shaking.
- Bead beating: Cells are agitated in the presence of small beads, which physically break the cell walls upon impact.
- Freeze-thaw cycles: These exploit the expansion of water when it freezes to disrupt the cell membrane by repeatedly freezing and thawing the sample.
- Osmotic shock: A sudden change in solute concentration around the cells can lead to lysis due to the inflow or outflow of water as the cell attempts to balance osmotic pressures.
Each technique has its own merits and drawbacks, and often a combination of methods is used to achieve optimal cell disruption while preserving the integrity of the cellular components.