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• iGEM 2013

Contents 1 June 1.1 6/10/13 1.2 6/12/13 1.3 6/14/13 1.4 6/17/13 1.5 6/19/13 1.6 6/21/13

June

6/10/13

Today we looked at a paper describing efficient ways to propagate large phage. They suggested agarose instead of agar, and at a concentration of 0.15% which is 1.5 g/L. Dr. Grose explained to us that agarose is more stable and forms larger pores, requiring a smaller amount of powder to produce a solid, stable gel. LB Agarose top agar can be plated onto normal LB bottom agar. We will make up some agarose top agar and see what size of plaques we get.

Wednesday we will need to start an overnight culture in a 250 mL flask (using 25 mL of LB broth). We will a piece of a small colony and put it in the flask along with 20 ug of adenine per mL. It will incubate on the shaker until class starts.

6/12/13

Results from 6/10/13 Unfortunately none of our agarose media set up, even in the jars that were left on the counter. This was unfortunate because it meant our seven plates were unreadable. We will need to make a higher concentration of agarose to learn what it takes for agarose top agar to solidify on LB agar plates.

Today we started an E. coli B culture in a 250 mL flask, 25 mL LB broth, and 100 uL of adenine (final concentration 20 ug/mL). This grew from 9am until 3pm when we pelleted the bacteria at 3,000 rpm in a Sorvall centrifuge. The bacteria was resuspended in 25 mL of M9+ media. The OD600 reading of the resuspension was 0.617. In two 250 mL flasks, we mixed 6 mL of E. coli B in M9+ media, 1 mL of high titer lysate (~3x10^9 pfu), .5 mL of bromodeoxyuridine (final concentration 200 ug/mL), 100 uL adenine (final concentration 20 ug/mL) and 200 uL uracil (final concentration 20 ug/mL).

We let one flask incubate on a shaker for ___ hours (until _:__ pm) and the other incubate on a shaker for ___ hours (until _:__ pm). The bacteria was pelleted and the phage-containing supernatant was transferred to a new test tube and refridgerated at +4C.

KS and BDM

6/14/13

6/17/13

6/19/13

6/21/13