Tuesday was our field trip day. Dr. P. took us to the waste water treatment plant where we got to see and learn how waste water is safely treated before entering the river. The facility manager gave us all the tour. He took us through the facility along the path the water travels from where it enters to where it exists into the river. He told us all about the types of microbes that are use in the process (All the microbes are aerobic). It was amazing to see the details. It has definitely given me a great appreciation for the job that these men do. They are so smart!! He was telling us all about the chemical reactions that these microbes have and why this one is better than that one because it can be used up in the reaction so it never is released back into the environment. He completely lost me at some points, but it was really amazing. These men are so smart and I can thank them enough for the job they do.
I forgot my camera when we went so I'm sorry that there's no pictures.
Sunday, November 10, 2013
Thursday, October 24, 2013
Interesting...
So we have more results and possibly a contradictory one. Lets start with our Thioglycollate test which shows us the type of environment our bacteria can grow in. In our test tube, the bacteria grew all throughout the tube! This told us that our bacteria H has facilitated growth meaning it can grow with or without oxygen in the environment.
![]() |
| So it's hard to see, but there is bacteria all throughout the tube |
Next we looked at our last enzyme test which was on DNA agar. We had to add hydrochloric acid to the plate in order to see the result.
Now we will look at our last five tests. These were all on selective or differential media. They will tell us where our bacteria can grow.
First is blood agar. Our bacteria grew, but did not have the ability to lyse red blood cells (in other word break them down).
The next one was EMB (eosin methylene blue). This one was negative as it was lacking any growth what so ever. Some of these tests we don't know yet what the results mean, but Dr. P. assured us that we will be learning about it in lecture soon.
The Mannitol Salt agar was then under scrutiny. Since this agar is a salt most bacteria won't grow here because of the hypertonic state. The salt will draw all the water out of the bacteria and it will die. This is why pickled foods last so long because lots os bacteria cannot grow in the salty environment. Our bacteria is the one above the line and it did not survive.
Our fourth one is the MacConkey agar. This one is suppose to inhibit gram-positive bacteria. Other then that all we know it that we had no growth. What this result means, again we do not know yet.
The fifth and final test to look at was the PEA test (Phenylethyl Alcohol Agar). This one was interesting because this agar inhibits or slows gram-negative growth. We beleaved that from our gram stain that our bacteria was gram-negative. The problem though is that we has growth on this plate!!
The amount is very small so it could be that our mystery H bacteria was still able in some way to grow just a tiny bit, but it still makes us question if our original thoughts was wrong. Next week we may repeat the gram stain and see if we still come up with the same results. Until then, have a safe weekend!!
Tuesday, October 22, 2013
More samples and Strep throat swabbing practice
We are now half way through our tests for our mystery bacteria H. Today we looked at the streak plate we did last week. The bacteria grew on the surface so it must be aerobic. To see if bacteria H has any peroxisomes we poured hydrogen peroxide on the surface of the plate. Our's was slow to bubble, but after a few seconds it started to react. This told us that our bacteria is definitely aerobic because the catalyst needs to be present in order for there to be oxygen for the bacteria to grow.
We also inoculated seven more tests. Five of them are called differential media tests, one was to test for the hydrolytic enzymes for DNA, and one was to test the anaerobic or aerobic type of bacteria.
The five test we started on different media were:
EMB, Blood, PE, Mannitol Salt Agar, and MacConkey Agar

We got to be all official and use the disposable tips to inoculate!!
So the last thing we did was practice swabbing each other's throats for strep. We didn't test them all, but we got to practice the technique. It was super fun. hardly anyone gagged so I hope we did it right! Anyway, on Thursday we will see if our bacteria has decided to be interesting or not. We shall see.
![]() |
| We shared our plate with another group so our bacteria is the yellow one. |
We also inoculated seven more tests. Five of them are called differential media tests, one was to test for the hydrolytic enzymes for DNA, and one was to test the anaerobic or aerobic type of bacteria.
![]() |
| Anaerobic or Aerobic? After inoculating |
![]() |
| Anaerobic or Aerobic? Before inoculating |
The five test we started on different media were:
EMB, Blood, PE, Mannitol Salt Agar, and MacConkey Agar
We got to be all official and use the disposable tips to inoculate!!
So the last thing we did was practice swabbing each other's throats for strep. We didn't test them all, but we got to practice the technique. It was super fun. hardly anyone gagged so I hope we did it right! Anyway, on Thursday we will see if our bacteria has decided to be interesting or not. We shall see.
Monday, October 21, 2013
Urea! Things are looking up.
Thursday, October 17th
WE FINALLY HAVE A POSITIVE TEST!!!!
Our test for Urea came back positive. Because of this we can conclude that our bacteria can hydrolyze urea.
Not surprising however, the rest of our tests came back negative. Here's a couple of examples of our negative tests:
Nitrate: Indole:

After we checked our test results we completed an oxidase test.

Our results came back negative:
Classic Bacteria
Tuesday, October 15th
We got our results back today from the sucrose, lactose, glucose, and TSI tests and the verdict is........
....*drumroll please*....
ALL NEGATIVE.
This is a classic occurrence for our unknown bacteria. It's a stubborn one!
Here's some pictures from our negative results:
Sucrose:
Glucose:
TSI:
Indole
Urea
Nitrate
MR
Citrate
TSA
Indole:

Urea:
Nitrate:
Methyl Red (MR):
Citrate:
More results to come on Thursday! Maybe next time we will finally get a positive test. We'll have to wait and see!
Tuesday, October 8, 2013
Test Results!!!
So, at the end of last week we prepared five different tests to see if our unknown bacteria H had any hydrolytic enzymes (digestive enzymes). The results though were less then impressive though. Here they are:
Starch test: Negative
Casein Test: Negative
Lipid Test: Negative
Gelatin Test: Negative
Litmus Milk: Negative
Here are the pictures
Starch test: Negative
Casein Test: Negative
Lipid Test: Negative
Gelatin Test: Negative
Litmus Milk: Negative
Here are the pictures
![]() |
| Lipid Test |
![]() |
| Casein Test |
![]() |
| Litmus Milk Test |
| Starch Test |
![]() |
| Gelatin Test |
So we basically decided that our bacteria is boring. Anyway, not much came from those tests. This bacteria is really resisting our detective efforts. Well, we won't be discouraged! The last thing we did was prepare one more series of tests. These were to see if our bacteria breaks down any sugars. We tested Glucose, Fructose, Lactose, and triple sugar iron.
Hopefully we get some results!
Monday, October 7, 2013
A Whole Buch of Tests!
Thursday October 3, 2013
First discovery of the day was that our bacteria was not motile. Unfortunately, it looked about the same as it did on Tuesday. We were pretty bummed, we wanted to see it move under the microscope!
Next we completed several inoculations to test for starch hydrolysis, casein hydrolysis, fat hydrolysis, litmus milk, and gelatin hydrolysis.
Starch hydrolysis:
Casein Hydrolysis:
Fat Hydrolysis:
Litmus Milk test:
Gelatin Hydrolysis:

After we completed the inoculations, we stored the bacteria at 25 degrees Celsius.
We then looked at the broth inoculation we had done on tuesday, and at first didn't see any bacteria growing. We reinoculated our bacteria in the broth.
After that, Dr. P came over and told us that we actually did have bacteria growing! Pretty awesome. We then practiced the droplet slide technique under the microscope. Adios!
Subscribe to:
Posts (Atom)































