Team:Hawaii/Notebook/2008-05-24

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(Difference between revisions)
(Margaret: finish notebook)
(Discussion: marg. update notebook)
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* If our action is not recorded, we are doomed to either repeat the error, or fail to replicate the success.
* If our action is not recorded, we are doomed to either repeat the error, or fail to replicate the success.
<blockquote>''History is the only laboratory we have in which to test the consequences of thought.'' - Étienne Gilson</blockquote>
<blockquote>''History is the only laboratory we have in which to test the consequences of thought.'' - Étienne Gilson</blockquote>
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== Update on Seed Stocks ==
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* The seed stocks are forming a nice lawn on the media
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[[Image:platecultures.jpg]]
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== Update on Clumping ==
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* The homogeneous culture is now clumping. Clumps are reverting to homogeneous
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[[Image:homogeneoustoclump.jpg]]
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[[Image:declumpingupdate.jpg]]
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Revision as of 19:26, 27 May 2008

Contents

Margaret

Made seed stocks

  1. five 10mL seed stocks of PCC6803 in BG-11 media
  2. five plates smeared with 200uL PCC6803 in BG-11 media, all from old plates

Hypothesis: Liquid Cultures of PCC6803 clump when incubated in Erlenmeyer Flasks and does not when cultured in 'box' culture flasks: Is this due to the motion of the media in different containers, the surface area of the culture, is it reproducible?

  1. Question 1: Does the clump go back to homogeneous when placed in square culture flask?
    1. Test: Took 0.5mL of a clump and placed it in 2 square culture bottles. (1 of the bottles was fresh BG-11 media, the other was the old stock to which buffer was added today)
    2. Compare to: Took 0.5mL of a homogeneous liquid culture and placed it in 2 square culture bottles. (1 of the bottles was fresh BG-11 media, the other 1 was the old stock to which buffer was added today)
  2. Question 2:Will previously homogeneous culture go to clump?
    1. Homogeneous liquid culture placed in BG-11 media in an Erlenmeyer flask 1:10, Vfinal=50 mL
    2. Homogeneous liquid culture placed in BG-11 media in an Culture flask 1:10, Vfinal=50 mL

Declumping test nodetail.jpg Declumping test detail1.jpg Declumping detail clump.jpg Homogeneous to clump 50mL.jpg

Discussion

  1. What to do in the future:
    1. The plates are drying out too soon so we need to make them 5mm thick instead of 3mm thick.
    2. Get autoclave certification. We need to make media and autoclave hood materials: paper towels (?), eppendorf tubes, blocks, etc.
    3. Get Pictures!
  • If our action is not recorded, we are doomed to either repeat the error, or fail to replicate the success.
History is the only laboratory we have in which to test the consequences of thought. - Étienne Gilson

Update on Seed Stocks

  • The seed stocks are forming a nice lawn on the media

Platecultures.jpg

Update on Clumping

  • The homogeneous culture is now clumping. Clumps are reverting to homogeneous

Homogeneoustoclump.jpg Declumpingupdate.jpg