A disadvantage of the streak plate technique could be colony isolation problems. If the streaking technique is not done properly or if there is too much of an organism present on the inoculating loop then the cells can cluster and form what looks like one colony but it can actually be a couple colonies (made from a couple cells). This can cause an inaccurate colony forming unit count.
In scientific circles, the streak plate method is considered to be a rapid qualitative isolation method. To be effective, one must reduce the number of organisms in the inoculums by spreading a loop of culture over an agar plate. This ensures that individual cells are properly separated on the surface for the purpose of differentiating various species. The method is as follows: Using a sterile loop, microbes are initially transferred to the plate with one swipe. On the subsequent swipes, the loop is heated in the flame of a Bunsen burner to lessen the population of microbes being transmitted. Streak patterns are also done in via T-streak or by applying the loop to four quadrants of the plate.
One fail safe way to obtain a pure culture is the streak plate method. This is the best of several ways to obtain a PC. Streak plates allow us to isolate a particular microbe from a mixed culture. A small amount of desired microbe is obtained with a sterile loop, and a single colony is grown on a separate quadrant of the agar plate, or ideally another agar plate all together. One advantage to this method is that a skilled student can, if experienced and skilled, recolonize one particular type of bacteria/microbe up to three times on one agar plate, wherefore less materials are used. Another significant benefit is that this is one of the quickest methods. Another method of obtaining a pure culture is the pour plate method. Pour plating is a method of separating one species of bacteria from another by diluting one loopful of organism into three liquefied nutrient agar plates, with the hopes that one of the plates poured will provide an ideal sample for isolation. An advantage to this method is that it requires far less skill than the first method, however requires far more materials and time.
Bacterial mixture is transferred to the edge of an agar plate with an inoculating loop and then streaked out in one of several patterns. At some point, individual cells will be removed from the loop and will give rise to separate colonies.source: http://quizlet.com/17578430/micro-lab-unit-1ex-15-16-streak-plate-technique-flash-cards/
1 The Spread Plate: If a mixture of cells is spread out on an agar surface so that every cell grows into a completely separate colony, a macroscopically visible growth or cluster of microorganisms on a solid medium, each colony represents a pure culture. The spread plate is an easy, direct way of achieving this 2 The Pour Plate: Extensively used with bacteria and fungi, a pour plate also can yield isolated colonies. The original sample is diluted several times to reduce the microbial population sufficiently to obtain separate colonies when plating result. 3 The streak plate: Pure colonies also can be obtained from streak plates. The microbial mixture is transferred to the edge of an agar plate with an inoculating loop or swab and then streaked out over the surface in several patterns
It depends, if there is no growth or colony appearance on streak line and only it shows growth in b/w the streak line then it is certainly a contamination and if there are colonies on streak line and not ressemble with the streak culture then also it is a contamination but there can be a chance that colony appears due to some fault in streaking procedure and the inoculum drops between the streak line so it depends.
The streak plate method makes it easier for colonies of bacteria to grow. It also generally leads to individual colonies that look like small dots, rather then simply a mat of bacterial growth.
The streak plate method makes it easier for colonies of bacteria to grow. It also generally leads to individual colonies that look like small dots, rather then simply a mat of bacterial growth.
The streak plate method is preferred over spot inoculations because it allows for the isolation of individual colonies from a mixed culture, promoting the separation of different microorganisms. This technique creates a gradient of dilution across the agar plate, enabling the growth of distinct colonies that can be easily identified and characterized. Additionally, the streak plate method minimizes the risk of contamination and provides a more systematic approach to isolating pure cultures.
It is more likely to give individual colonies regardless of the concentration of the original source. With pour plates, you might have to use several plates with different dilutions of inoculum to get individual colonies.
In scientific circles, the streak plate method is considered to be a rapid qualitative isolation method. To be effective, one must reduce the number of organisms in the inoculums by spreading a loop of culture over an agar plate. This ensures that individual cells are properly separated on the surface for the purpose of differentiating various species. The method is as follows: Using a sterile loop, microbes are initially transferred to the plate with one swipe. On the subsequent swipes, the loop is heated in the flame of a Bunsen burner to lessen the population of microbes being transmitted. Streak patterns are also done in via T-streak or by applying the loop to four quadrants of the plate.
The simplest technique for isolating bacteria in growth media is referred to as streak plating. In streak plating, a small sample containing mixed bacterial populations is spread in a pattern over the surface of an agar plate, allowing individual bacterial colonies to form and grow separately.
The streak of a mineral can be determined by rubbing the mineral against an unglazed porcelain tile to produce a powder. The color of the powder left behind is the streak color of the mineral. It is important to use a streak plate or tile with a hardness greater than the mineral being tested to prevent contamination.
To test out a streak, you can observe the behavior consistently for a period of time to see if it continues. For example, if you want to test if a winning streak in a game is genuine, keep track of the wins over multiple sessions. If the streak persists consistently, it is likely a true streak.
One fail safe way to obtain a pure culture is the streak plate method. This is the best of several ways to obtain a PC. Streak plates allow us to isolate a particular microbe from a mixed culture. A small amount of desired microbe is obtained with a sterile loop, and a single colony is grown on a separate quadrant of the agar plate, or ideally another agar plate all together. One advantage to this method is that a skilled student can, if experienced and skilled, recolonize one particular type of bacteria/microbe up to three times on one agar plate, wherefore less materials are used. Another significant benefit is that this is one of the quickest methods. Another method of obtaining a pure culture is the pour plate method. Pour plating is a method of separating one species of bacteria from another by diluting one loopful of organism into three liquefied nutrient agar plates, with the hopes that one of the plates poured will provide an ideal sample for isolation. An advantage to this method is that it requires far less skill than the first method, however requires far more materials and time.
Previous answer: "because of infection" This person is obviously trying to be funny, the right word should be "Contamination", as for spread plate, the bacteria is more exposed to air as it is spread over the agar plate. Therefore, the result might not be accurate, as it might be contaminated. As for the pour plate method, the bacteria is in the agar itself, it is not exposed to air, thus, less risk of getting contaminated.
Instantaneous results. The primary advantage of the photographic plate over CCDs is image quality--an 8x10 plate carries a lot more image information than a CCD can capture.
A streak plate technique is used to isolate a single species from a mixed species population. You take a small sample of the mixed species on a sterile loop and streak an agar medium into four zones, reflaming the loop between zones. After incubation, single species colonies should be visible within the fourth zone.