| Morning Session: Bringing DNA to
the Classroom |
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| Zuzana Zachar discussed changes in the National
Education Standards, the Teacher Training program at Stony
Brook, and an overview of the DNA workshop. |
Pat Bossert discussed the importance of
hands-on activities that elicit inquiry-based learning. |
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| Judi Heitz described the program at her
school: Biotechnology in the Secondary School. |
The first experiment involved isolating
DNA from fruit flies. Here, a student is grinding
dead fruit flies in a buffer solution. |
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| After grinding, INSTAGENETM
beads are added to the tube to bind proteins and lipids..
Dr. Bossert is explaining the principle of INSTAGENETM
beads: the beads are made of a negatively charged
matrix. Proteins and lipids are mostly positive
and therefore will bind to the beads. DNA remains
in the supernatant. |
Tubes are placed in the thermocycler that
is set at 65 C and incubated for 10 min. The cycler
is then set to 99 C and the tubes are incubated for an
additional 10 minutes. The heating steps are used
to break open the cells and to denature proteins.
Denaturation caused the proteins to dissociate from DNA. |
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| After heating, the tubes are allowed to
cool and the beads are allowed to settle out. The
supernatant, which contains the DNA is pipetted to a fresh
tube. Here, Dr. Zacher is demonstrating how to use
a micropipettor. |
Students are practicing pipetting. |
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| 10 ul of DNA solution is mixed with a blue
dye and then loaded into wells of an agarose gel. The
gel is placed in an electrophoresis chamber and subjected
to electric current which separates the fragments of DNA. |
The bands in the photo show the different
DNA fragments........... |
| Student Presentations |
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| Afternoon Session: Plant Tissue Culture
in the Classroom |
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| Dr. Ken Torres gave an overview on plant
tissue culture. |
Dr. Carol Stiff gave a presentation on how
to do plant tissue culture in the classroom using inexpensive
equipment. |
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| Using simple equipment such as plastic pitchers,
pint jars, dish detergent, commercial bleac, Dr. Stiff
showed how to disinfect African violet leaves. |
Following the demonstration, students disinfested
leaves and cultured them on media. |
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| Students are preparing disinfested leaves
for in vitro culture. |
This student got to use a "clean box" for
his experiments. |
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| Dr. Michael Kane gave an overview of the
plant tissue culture program at the University of Florida
including his upcoming workshop for K-12 teachers. |
Here a student is transferring internode
sections of Parrot feather to media containing hormones. |
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| This is an internode section of Parrot feather. |
This internode section has been cultured
for 5 days on media containing plant growth regulators.
Note the new shoots developing - this is called organogenesis. |
| This workshop showed how biotechnology
techniques, DNA isolation and analysis, and plant
tissue cultue, can be accomplished in a high school classroom
with inexpensive equipment and supplies, safe chemicals,
and minimal training. The student presenters proved that
these techniques can be utilized in the classroom and
can be easily accomplished by the students. These
techniques encourage inquiry based learning at the high
school and college level. |