-
Discussion
|
Organism
|
Result
|
pos1
|
YEAST
|
pos2
|
YEAST
|
pos3
|
YEAST |
This
is actually yeast. On GYC Standard medium.
|
|
|
|
|
|
Pos1, pos2 and pos3, upon
microscopic observation, turned out to be yeasts. Their macroscopic
morphology strongly resembled that of Gluconobacter but the cells
were too large to be bacteria.
|
|
|
|
|
|
Test
|
pos4
|
pos5
|
Gluconobacter
|
Gram
Stain
|
-
|
-
|
-
|
Lactose
Fermentation
|
-
|
-
|
-
|
Glucose
Fermentation
|
+
|
+
|
-
|
Gel
Liquefication
|
-
|
-
|
-
|
Indole
Production
|
-
|
-
|
-
|
Nitrate
Reduction
|
+
|
-
|
-
|
H2S
Formation
|
-
|
-
|
-
|
Catalase
|
+
|
+
|
+
|
Oxidase
|
-
|
-
|
-
|
Motility
|
-
|
-
|
+/-
|
Pos4 and pos5 strongly resemble
Gluconobacter in the above chemical tests.
Gluconobacter is
supposed to grow
in pale, milky white colonies. Pos4 is slimy and yellow and does not
fit the stated morphology. Pos5, on the other hand, grew in small
regular circles and had a pink tint on mannitol and MacConkey's medium.
Bergey's Manual said that some Gluconobacter strains
could be pink, and thus pos5 fits the description most properly.
|
|
|
|
pos4
gram stain
|
|
|
pos5
gram stain
|
|
|
|
|
pos4
on Frateur's medium
|
|
|
pos5
on Frateur's medium
|
It can definitely be said
that this has been a learning experience. We have determined successfully
the steps one needs to follow in order to isolate Gluconobacter.
Although not all of the results matched the genus Gluconobacter,
we feel confident that we have isolated an organism very close to
it. We learned that any medium that calls for calcium carbonate needs
extremely well ground crystals, as otherwise they will not stay in
the medium but will settle to the bottom of the plate, where growing
bacteria cannot reach it.
- Ecological
and Biotechnological Importance
Gluconobacter is usually found
in fruits and flowers, as well as baker's yeast, beer, wine and cider.
Strains are used industrially to produce L-sorbose from D-sorbitol,
D-gluconic acid, 5-keto- and 2-ketogluconic acids from D-glucose, and
dihydroxyacetone from glycerol. Recently the strain Gluconobacter
oxydans has been used as a bio-sensor in the mass-production of
ethanol. Certain strains will detect the presence of xylose, a valuable
coproduct in the ethanol production process, more efficiently, and therefore
more cost-effectively, than others. A protocol such as ours for isolating
strains of Gluconobacter could be valuable in the continuing
search for new and more efficent strains.
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