Streak Plate And Viable Cell Count

Streak shield And practicable Cell CountAim and introduction should display taste into what the cake plate and viable cell count effectuate atomic bit 18 employed to win. They should similarly introduce MacConkey nutrient nutrient nutrient agar-agar-agar-agar and how its selective and differential properties bear the characteristics of the test organism to be determined.Escherichia coli (E.coli)The aim of this sample is to surrender a certain bacterium to divide and multiply enabling us to get word the bacterium in a single cell structure. E.coli is one bacterium that is good for such an examine. E.coli fire be said to be twain bad and inoffensive, nigh E.coli bacterium flip are highly toxicant and can harm kinds and animals. However, the majority of E.coli strains are relatively harmless with low toxicity. These harmless strains of E.coli are found naturally occurring in the human body, especially in areas such as the human intestines. Some E.coli can rase benefit their hosts they do this by producing specific vitamins. It is for movements like the ones mentioned why E.coli is an appropriate bacterium to use for this experiment. Another reason is that E.coli bacteriuml cells have an honest bacterial size of 2um this can be seen on a lower floor a light microscope. Other bacteria more than than than(prenominal)oer may be even smaller and may require a larger microscope for regard or even an electron microscope. Also the incubation period for E.coli to multiply and let rapidly isnt very long and temperatures arent likewise high or too low. E.coli can be incubated overwickedness at 37oC and and so stored at 4oC until its requirement.The proficiency use to manipulate and isolate the E. coli bacteria is known as the streak plate surgery. The proficiency was genuine to allow bacteria to multiply and introduce many another(prenominal)(prenominal) an(prenominal) colonies, during the incubation period, depending o n the amount of bacteria shew. Each dependence will contain millions of bacteria cells derived from a single parent cell. (Talk in more detail about this procedure). We will be exploitation this technique to allow the E. coli to multiply and divide splitting itself into colonies.The viable cell count, overly known as vi cleverness count, is a rule apply to determine the topic of living cells within a suspension, in this case E. coli. To obtain an fellow feeling of how much E. coli cells are present in a deterrent example this order must be put into execution. (Expand)The MacConkey agar is specifically designed to allow gibibyte detrimental bacteria to grow its a recipe of many substances such as bile salts, sodium chloride proteose and many more. One of the properties of the MacConkey agar is its selective isolation and identification of bacteria it is a medium that allows us to distinguish gram-negative bacteria. E. coli is a rod shaped gram negative bacteria, so vic timization the MacConkey agar plate to multiply it would be appropriate, the agar will also cause the E. coli to change food tincting from pink to red, and this is an characteristic of gram negative bacteria present.A Nutrient agar is a growth medium utilize for the cultivation of bacteria, this specific agar form solid even at high temperatures. The gram- marking technique was developed for run intoing cells clearly under(a) a microscope and to enable us to establish their structures. It is a very simple procedure of just adding 4 different substances accordingly, however one of these substances is toxic to humans in that respectfore the procedure must be carried out in a fume hood. The gram stain method was introduced byIt is important for scientists and medics to know the structure and function and identity of bacteria and viruses, it is for reasons like this why such experiments are carried out. Without such procedures so many bacteria and viruses wouldnt be known and could spread and become out of control.Methods pardon why from each one procedure was through with(p) highlight key points recount any deviation from protocol document any errors or difficulties you had with the techniqueDiscuss the importance of unimaginative technique and what steps could be interpreted to prevent contamination during manipulation of bacteriaAll methods were doing under aseptic conditions the reason for this is to prevent contamination of the bacteria during its manipulation. Many errors could arise if aseptic conditions arent used, eventually upshoting is wrote results.Streaking bacteria on MacConkey agar methodPrior to the experiment, an E. coli sample was made and given to during the practical.Risk assessmentMaterials used10ml eloquent destination of E. coli the bacteria sample to be use in this practical sterilised tensile circulates used for transferring E.coli bacteria from one place to another uncontaminated.MacConkey agar plate used to all ow E.coli bacteria to grow as it provides skill recourses and supportSharps bin for loop-the-loops etc. these are used to keep the testing ground area as uncontaminated as possible and to make original bacteria doesnt spreadMarker pens and labels to label the plateStep 1 using a barren plastic loop I affected a given sample of E. coli and streaked an inoculum onto a MacConkey agar plate in a specific pattern (see..). This plastic loop is then disposed of into the sharps bin.Step 2 using another sterile plastic loop, I created a run of parallel lines from the edge of the initial streaksStep 3 step 2 was repeated 2 more times with a new-made sterile loop used.Step 4 a last-place streak was made, creating a simple streak from the foregoing streaks into the centre of the plate. The picture below illustrates this.The MacConkey plate was then given to the technicians to incubate.It was important to dispose- on the plastic odors by placing them into the sharps bin because they ar e contaminated and if they converge any other surface it can lead to the spread of bacteria resulting in major contamination. passim this procedure plastic gloves and a lab-coat were worn, also to prevent contamination.Viable cell countsRisk assessmentMaterials usedP1000 and P100 pipettes and tips used to transfer certain amounts of PBS etc.Three Nutrient agar plates10ml sterile PBS archetype, used to maintain the pHSterile plastic spreaders to spread the E.coli on the Nutrient agar platesEight sterile bijoux bottles for dilutionsTo get cracking the dilution, using a pipette I transferred 900 ul of diluents (PBS) in eight different sterile bijoux bottles. The PBS (phosphate buffered solution) solution is a comm wholly used buffer to maintain a pH it is used in this practical because of its ability to aid biological research. later on the PBS was fixed into the labelled bottles, using a new sterile tip for the pipette I transferred 0.1ml of E.coli liquid husbandry sample ( neat) into the first bottle (10-1). For the dilution to continue a new pipette tip was placed and 0.1ml of the 10-1 diluted E.coli was transferred to the 10-2 bottle, this process continued up till bottle 10-8. By doing so the E.coli will become more and more dilute within the different solutions, because less E.coli is being added each time. 10-5, 10-6 and 10-7 samples were then spread onto three different Nutrient agar plates using different sterile plastic spreaders so contamination wouldnt occur. This was done by placing 0.1ml of each dilution onto the centre of the agar plate and then spreading it over with a sterile spreader. The agar plates were labelled and given to the technician for incubation. thousand office of bacteria from an isolated resolutionRisk assessmentIn order to stain the bacteria I selected an appropriate colony to stain, the colony must appear to be uncontaminated and its coming into court must obviously look grown.. After this procedure is drop, the bac terial cells will be visible under a microscope.Materials neededBunsen burner used to heat-fix bacteria onto microscope parachute saline (PBS) emulsifierLight microscope to view bacterial cellsLens tissue to clean the electron lensImmersion oil for light microscope lens to allow better view at 100x magnification patchs for chiliad stain methodBefore the bacteria can be modified to be viewed under the microscope clearly, the microscope glass slide must be cleaned to prevent contamination. After doing so a exuviate of sterile saline was placed onto the centre of the slide, the saline drop was placed because it can emulsify any bacterial colony that will be placed on top. To move some of the bacteria off the agar plate onto the slide, a sterile loop was used I stirred the bacterial colony on the agar plate with the top of the loop and then spread the bacteria into the saline drop making it thin. collectible to the moisture of the liquid I let the slide dry then used a Buns en-burner to heat-fix the bacteria onto the slide by passing it finished a few times then allowing it to cool. Heat-fixing was done so that during the spot the bacteria or wouldnt move or fall off. Once that was complete the slide was moved to a laboratory fume hood where the maculation can take place, the follow 4 stop method was used at first the bacteria sample on the slide was strong in crystal violet for 30 seconds, aft(prenominal) so it was rinsed with distilled body of water and drained. The second subtract is to soak the bacteria with gram single (mordant) for another 30 seconds then rinse with distilled water and drain it. thousand iodine is a toxic substance it is for this particular reason why this part of the practical was carried out in a laboratory fume hood. propanone de commentiser was then added for 10 second and the bacteria was over again rinsed with distilled water and drained. The final part is to add Safranin, a counter stain, to the bacteria. It w as placed on the bacteria for 30seconds and then the bacteria was further rinsed with distilled water, drained, defectted and allowed to dry.SubstanceDurationFurther actionCrystal violet (primary stain)30 secondsRinse with water drain yard Iodine ( caustic)30 secondsRinse with water drain propanone/alcoholic beverage (Decolouriser)5-10 secondsRinse with water drainSafranin (Counter stain)30 secondsRinse with water, drain, blot dryStain was carried out in a laboratory fume hood due to the toxic gram iodine substance used. The liquid plastic shield of the fume hood was lowered so that only my hands were inside dealing with the chemical and biological substances. Gloves were worn during this procedure so that no stain would come into contact with the skin. When the slide was rinsed with water, it was rinsed piano with distilled water so that the bacteria are not shifted.After the detection was completed the sample can now be viewed under a light microscope and compared to other bacterial samples. The slide is placed on the stage with a drop of oil for immersion, the microscope is focused on 100x and the bacteria is viewed.ResultsShould suck up your findings in prose/text, diagrams, tables and graphs which includes a description of growth characteristics and how successful your aseptic technique wasMacConkey agar plate resultsDuring the experiment there were no results to be state as it was too early for anything to occur. After the agar plate containing the E.coli was incubated at 37oC and then stored at 4oC, its demeanor was as expected. Colonies were separated, and as the streaks moved on less E.coli was present. The colonies were well distinctive and were round in their shape. The sample ab initio given was simply liquid, the result showed significant growth of this E.coli liquid into 3D structures. This indicates the growth of the bacteria in a fine way the 3D structures appeared in a yellowing solid colour. Because the practical was conducted in aseptic techniques no contamination occurred. Aseptic techniques were successful in allowing me to produce accurate results.Viable cell countsMy resultsThe colonies that appeared on the nutrient plate had a badge colour visually they all appeared relatively same sized and volume.10-510-610-710-8TMTC461For the 10-7 the calculation for the number of bacteria in 1ml of the original culture is(1107/0.1) x (X/1) cross multiply0.1X = 1 x(1107) divide by 0.1 therefrom X = 1.0108For the 10-6 the calculation for the number of bacteria in 1ml of the original culture is(46106/0.1) x (X/1) cross multiply0.1X = 1 x(46106) divide by 0.1Therefore X = 4.6108The number of bacteria present in 1ml of the 10-5 culture cannot be calculated as there was no value acknowledged (TMTC).X= number of bacteria. The number of bacteria present in 1ml of 10-6 dilution is 4.6108 and in the 10-7 dilution culture is 1.0108.Class resultsPair number10-510-610-710-81TMTC461295903TMTC5294TMTC23153426841147TMTC241882226 91026010193311TMTC1401512TMTC57913611201486115195514165527317TMTC941118TMTCTMTCTMTC19TMTCTMTCTMTC20TMTC11318Total26698517728Average66.557.99.87Should constitute your findings in prose/text, diagrams, tables and graphs which includes a description of growth characteristics and how successful your aseptic technique wasTo determine the amount of bacteria within a culture a simple calculation must be done using my idiosyncratic(prenominal) results for this experiment. There was no value for the 10-5 so this cannot be done.The result for 10-6 was 46, 46 x 10 = 460ml. To estimate the amount of E.coli present this is further compute by 106, therefore 460 x 106 =For the 10-7 result 7 x 10 = 10 10 x 107 =However, I have selected some average results from the table to calculate an average.Gram-stain of bacteria from an isolated colony (view method number 3)Gram stains help us distinguish between microbial organisms, for example gram negative bacteria and gram verifyatory bacteria. T his method was developed to know the identity of bacteria present. (See procedure for The Gram Stain in the methods section).During step 5 of the Gram Strain Method above the quest results were made when applying the four different substancesSubstanceColour after stainCrystal violet (primary stain)PurpleGram Iodine (Mordant)PurpleAcetone/alcohol (Decolouriser)Transparent (dye was washed off)Safranin (Counter stain)Reddish-pinkThe appearance of the E.coli bacteria under a microscope with 100x magnification was quite clear it had a rod-like structure with a reddish-pink colour. The rods were all more or less the same size, however some were packed together and others were on their own.DiscussionWere the results the expected? Did the methods adopted achieve their aim? How the experiments could be improved. Include background information, critical evaluation of resultsThroughout all the experiments and procedures a lab-coat and gloves were worn to avoid skin contact with bacteria and h armful substances. Overall the aims were accomplished and the results were as predicted.MacConkey agarThe colonies were expected to be in such a form, indicating that it was E.coli present and that it has rapidly multiplied into individual colonies. This further suggests that when E.coli is present under conditions where it could multiply, it multiplies by forming a round colony and expanding from there. However, some of the colonies were stuck together making it difficult to count the number of them present. What this meaning is that the growth of the bacteria was a success and the method adopted was accurate. The reason why some colonies were packed together may be the result of pressing too hard on the agar while streaking, with more streaking practice more accurate results can be obtained with colonies being on their own. The methods adopted for this practical achieved what was aimed for. After the incubation of the MacConkey agar plate the plate was stored for a week at a temp erature of 4oC, this may have changed the appearance in colour and in shape of the formed colonies. Contamination of the agar plate may have even occurred. An improvement to the experiment is to note down results straight after incubation is finished.Gram Stain resultsAfter analysing the microscope slide which contains the Gram Stained E.coli under the microscope its features were obvious. There were many average sized rods with a reddish-pink colour, some of these rods were packed together whist others were separated. canvas this with another prepared sample of B.subtilis, the B.subtilis was a violet colour and has a longer and curved shape, like fine threads. However some again were packed together and others separated.The purple colour of the B.subtilis indicates that it is gram positive, and the pink colour of E.coli indicates its gram negative. When the Gram Stain method was applied to the B.subtilis it obviously stayed purple though out, with E.coli it will decolourise once the decolouriser is added. The gram stain method is highly effective and efficient when dealing with different bacteria it helps mark them to a great extent. B.subtilis system purple throughout the Gram Stain procedure, this itself can be an indication that it is a Gram positive bacteria.bacterial cells have different types of cell walls, the gram negative and gram positive terms describe the nature of their structural differences. One of the important differences is that Gram positive bacteria have no outer membrane whereas Gram negative bacteria do, the purpose of this outer layer is to cover the peptidoglycan layer. When staining occurs the outer membrane of a gram positive bacterial cell wall becomes permanently stained as the strain can soft penetrate the thick peptidoglycan layer, so that if a decolouriser or distilled water is added the colour will remain purple. In the case of the gram negative bacterial cell wall the stain gets attached to the far outer membrane layer (l ipopolysaccharide and protein), this layer decreases the penetration depth of the strain on the peptidoglycan, so the stain can be decolourised or removed.The diagrams below illustrate this.Gram positive Primary stain Mordant Decolourisation Counter-stainNote colour remains the same throughout addition.Gram negativePrimary stain Mordant Decolourisation Counter-stainNote colour changes The aim of the Gram Stain method was confirm that the bacteria that was initially being dealt with was E.coli, after tests and results it confirmed that it was so the results were as expected and predicted.The methods used for this procedure were successful at achieving good results, however some can be altered. For example, the E.coli used for this experiment was used from experiment number one, not that that is a problem but when the E.coli was incubated over night and it had successfully multiplied it was stored at 4oC for quite a while (this experiment was carried out 1 week after the first one ). This possible may have altered the activity of the E.coli and also its appearance. Many resources state that gram negative bacteria should have a pink colour after the counter-stain has been added and rinsed off. In this case the E.coli bacteria in this experiment had quite a dark pink colour which was really close to the colour red, this appearance of colour was visual both with the naked eye and under the microscope as individual bacterial cells.Viable cell countsAs I predicted, the more dilute (10-8) solution will have less E.coli bacteria increase on its surface. As there were 20 different pairs doing the practical, and the dilutions were all done 20 times by different people, there is plenty path for error from contamination of inaccurate measurements.The 10-5 agar plates had many E.coli bacterial colonies increase on it, according to the results there was far too many bacteria that it was too many to count (TMTC). Gradually as the dilution increased the bacteria became l ess, 10-6 dilution had numbers ranging from 6-140. Obviously with such great difference within what is meant to be the same dilution there was some error/contamination present. The most obvious ones which had error are pair numbers 18 and 19 there was TMTC throughout (10-6, 10-7 and 10-8). What would be expected is that fewer bacteria should be present in the 10-8.