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Could some bacteria grow on the streak plate and not be seen using the pour plate technique?
Put simply - yes. Some strictly aerobic organisms will not grow in a pour plate. They may, however proliferate on a streak plate. Also consider the posibility of experimental error. The culture may have been added to the molten agar when it was too hot for the organisms to survive.
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What happens if you rub the mineral across a streak plate but the mineral does not leave a streak?
The lack of a streak would indicate that the mineral is harder than the streak plate, or the color of the streak is the same as the color of the streak plate.
Advantages of pour plate method over other methods of bacterial colony?
The purpose of the spread-plate technique is to grow and isolate colonies of bacteria. A sample of bacteria is transferred to the agar plate, an environment that provides nourishment for the bacteria to grow. The bacteria sample is applied to the agar plate which a special streaking technique that dilutes the amount of bacteria in each section of the agar plate continuously. This is because if you just swabbed the bacteria onto the plate with no special technique the colonies would grow very densely together and be difficult to study. The streaking technique gradually dilutes the amount of bacteria in each 'quadrant' of the plate, so the last quadrant should have small, isolated colonies that can be easily studied. The spread plate technique is also used for the eneumeration of aerobic microorganisms from the given sample. This can be done by serial diluting the samples, placing 0.1ml of the diluted sample in the middle of an agar plate and spreading the sample over the surface with a help of an L-rod. After the incubation rhe colonies can be counted.
What is meant by streak dilution technique?
The streak plate technique is a method of diluting bacteria down suficiently so that the will grow as single colonies. The technique varies from individual to individual so much so that you can identify a researcher's plates much like their handwritting! The technique is somewhat more standardised in hospital labs and a printed out sheet is placed below the plate for the operative to follow as a guide. The technique is usually taught like this; 1) Flame your loop and aseptically take 1 loopful of culture and place it a 12 o'clock on your plate draw a straight line 5cm across the plate ending around 2.30o'clock. 2) Lift the loop and draw two more lines parallel the first about 0.5 cm distance below the first. 3) Flame your loop. Turn the plate slightly anticlockwise and draw another set of 3 lines over lapping the first set. (your end at 5o'clock) 4) Flame your loop. Turn the plate slightly anticlockwise and draw another set of 3 lines overlapping the second set. (you end at 6.30o'clock) 5)Flame your loop. Turn the plate slightly anticlockwise and draw another set of 3 lines overlapping the third set. (your end at 8o'clock) 6) Flame your loop this time instead of a set of lines start by overlapping the fourth set of lines and then draw a scribble into the middle of your plate using as much of the unused agar as possible. The technique is sort of a dilution becasue each time you flame your loop it is sterilised, when you then draw out some of the bacteria from your last set of lines and spread them over a much greater area.
The calor a mineral leaves when it is rubbed across a plate?
Streak is the color of the finely powdered mineral when rubbed across a plate. Streak is one of the physical properties of minerals used to identify which specific mineral it is. Some minerals leave a completely different color streak than the original color of the whole mineral.
Compare the pour plate and streak plate methods of isolating bacteria?
I got the answer but you hav ta do your labreport yourself..haha Whoever wrote this is an a$$hole. I wish that you went to my school so I could kick your aXX..Ha ha back at you, jerk! thanks jerk,,that was really helpful.. anyway guys, here is the correct and precise answer, hope it will help u to complete ur lab repor..:) In streak plate method, After the first sector is streaked in dish, the inoculating loop is sterilized and an inoculum for the second sector is obtained from the first sector. The same is done for third and fourth sector. Thus this is a dilution process. Eventually, very few cells will be on inoculating loop, a single cell will drop from it as it is rubbed along the agar surface. These develop into separate colonies. Whereas, in the pour plate culture, sample is diluted several times to reduce the microbial population sufficiently to obtain separate colonies when plating. After the agar has hardened each cell is fixed in place and forms an individual colony.
What is the purpose of the streak for isolation?
By using streak plate technique to spread a clinical sample out on the surface of a growth medium individual types of bacteria can be isolated
What is the simplest technique for isolating bacteria in growth media is referred to as the?
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.
What explanation could be given for the failure of obtaining isolated coloni es on a streak plate?
Failure to obtain isolated colonies on a streak plate could be due to overcrowding on the plate, improper streaking technique, or contamination of the plate from the environment or the inoculation source. It is important to streak the plate in a way that allows for sufficient separation of individual colonies to form.
Why would bacterial colonies found in the first section of a streak plate but not on sections two and three?
If bacterial colonies are found only in the first section of a streak plate, it could be due to uneven streaking technique where the majority of the bacteria were deposited in the initial section. The subsequent sections may not have received enough bacterial cells to form visible colonies. It is important to ensure an even distribution of bacteria while streaking to obtain colonies throughout the plate.
1 how are microorganisms diluted and spread out to form individual colonies In the streak plate technique?
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/
What is the differences between a streak plate technique and a serial dilution technique?
A streak plate technique is used to isolate individual bacterial colonies on a solid agar plate to obtain pure cultures, while a serial dilution technique is used to dilute a bacterial sample in a series of steps to obtain a range of concentrations for further analysis. Streak plate technique is qualitative, focusing on colony isolation, while serial dilution technique is quantitative, focusing on estimating bacterial concentration.
Will isolated colonies of bacteria always be in the fourth sector on the streak plate?
No, isolated colonies of bacteria may not always be in the fourth sector on the streak plate. The placement of isolated colonies can vary depending on factors such as the distribution of bacteria on the plate and the streaking technique used.
What will a streak plate with two species of bacteria look like?
A streak plate with two species of bacteria will show separate colonies with distinct morphologies and colors. Each species will grow in its own isolated area on the plate, allowing for differentiation between them. It is important to observe and document the characteristics of each colony to identify and classify the bacteria present.
What is a streak plate?
A streak plate is a surface of unglazed ceramic, used to find the true color of a mineral specimen by drawing the specimen across it. The color of the resultant powder is referred to as the streak or streak color of a mineral.
Primary purpose of the streak plate?
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.
Will diamond leave a streak on a streak plate?
Diamond will not leave a streak on a porcelain streak plate because diamond is harder than the streak plate. It will leave a scratch on the streak plate for the same reason.
When would a microbiologist want to use the streak-to-grow method?
Plate streaking is often done to isolate a colony of bacteria. For instance, if a broth was grown with 2 or 3 different types of bacteria, it could be streaked out in a "3-phase streak." In a 3-phase streak the initial streak takes up a very small area (we draw a T on the back of the plate, this streak goes in the section above the T). The loop is flamed to kill off any bacteria still on it, then a couple streaks are made out of the original. This grabs some of the bacteria from that concentrated streak and spreads them out. This is repeated once more until the final streaks are less and less concentrated bacteria. When we incubate the plate we'll find lots of growth where the original streak was and less and less as we follow the path of the 3-phases. What you're looking for now is a single colony, off by itself. This can then be scraped off and plated on a separate plate and considered a "pure colony." Another usual time to use streak-to-grow bacteria is when you want to know the quantity or concentration of bacteria. You take maybe 0.1mL of solution and plate it, then count the number of colonies that form. Say you have 56 colonies, now you can say: 56 cfu (colony forming units) -------- 0.1 mL or 560 cfu/mL This is usual when testing to see whether a sterilization technique worked, or if a product is within the regulated levels of bacteria to be released the public, etc etc.
