Team:Yale/Our Project/Notebook/Week 5

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lab notebook: week 5 (7/5 -7/11)

• Monday 7/5--Colony PCR of Ligation Attempt #2 Transformants
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Colony PCR

• Ran colony PCR of colonies 1B-9B from ligation attempt #2 according to the same protocol as used on 7/1.
• Then ran a 1.0% agarose gel of the nine PCR reaction solutions against a 1 kb ladder, but the resulting gel failed to show any evidence of either insert or vector, so will have to rely on sequencing and digests of miniprepped plasmids.
Gel of colony PCR from ligation attempt #2 Lane 1: 1 kb ladder, Lanes 3-11:PCR products from colonies 1B-9B, in order

• Miniprepped liquid cultures grown from colonies of first ligation attempt (colonies 1A-4A) and second ligation attempt (colonies 1B-9B) according to standard miniprep protocol.

This day's activities are also recorded on page 47 and 48 of the hard copy lab notebook.
• Tuesday 7/6--Analysis of Results of Ligation Attempts 1 & 2
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More Diagnostics of Ligation Results

• In order to determine success of ligation attempts 1 and 2, digested the miniprepped plasmids 1A-4A and 1B-9B from 7/5 with XbaI and SpeI and then looked for evidence of two fragments, one at 3.2 kb and the other at 3.6 kb. Reactions were conducted for 2 hours at 37°C, with the following contents for each of the thirteen reactions

Component	Volume
Distilled Water	6.4 μL
10x NEB Buffer 4	2 μL
DNA solution	10 μL
NEB XbaI	0.8 μL
NEB SpeI	0.8 μL
Total	20 μL

• The diagnostic 1.0% agarose gel was run at 90 V vs. a 1 kb ladder. Each of the thirteen samples gave one diffuse band around 3 kb and no evidence of the 3.6 kb phsABC fragment, so both ligation attempts #1 and #2 were unsuccessful.
Gel of XbaI and SpeI double digest of plasmids from ligation attempts #1 and #2 Lane 1: 1 kb ladder, Lanes 2-5:1A-4A, Lanes 6-14: 1B-9B

• During digestion prepped plasmid samples for sequencing. Each sample contained 3 μL of plasmid soln (average concentration of 96 ng/μL), 2 μL of 4 mM VF2 (forward primer), and 13 μL of distilled water. Intended to follow up with reverse sequencing of more promising samples, but gel results made it a moot point.

Wetlab work for this day is also recorded on pages 47, 49, and 50 in the hard copy lab notebook.
• Wednesday 7/7--Triple ligation attempt--promoter + thiosulfate reductase + terminator
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Ligation Strategy

• Failure of previous two ligation efforts prompted rethinking of ligation strategy. Will attempt a one-step triple ligation that will link phsABC to B0015 and insert them both into a standard single-resistance iGEM background. phsABC will be digested with EcoRI and SpeI, B0015 with XbaI and PstI, and pSB1C3 with EcoRI and PstI, allowing for them all to be ligated together.

Prep work


• Needed more phsABC, so ran five PCR reactions to amplify it from plasmid pSB74. Reaction mixture contents were the same as the DMSO variant used on 6/30 as was the thermocycler protocol (phs50). The results were then run on a gel
Gel of PCR amplified phsABC Extreme right lane:1 kb ladder, all other lanes PCR reaction mixtures and their spillover
• Needed chloramphenicol plates for pSB1C3-based constructs, so mixed 350 μL of 50 μg/μL chloramphenicol with an autoclaved solution of 7.5 g agar and 12.5 g LB in 500 mL H2O and poured plates.
Digestions

• Ran all three digestion reactions for 30 minutes at 37 °C before heat killing for 20 minutes at 80 °C. Digestion mixtures had the following components:

Digestion Reaction Components
phsABC Digestion	B0015 Digestion	pSB1C3 Digestion
5 μL EcoRI Buffer 10x	5 μL NEB Buffer 3 10x	5 μL EcoRI Buffer 10x
0.5 μL BSA 100x	0.5 μL BSA 100x	0.5 μL BSA 100x
21.1 μL phsABC soln (1 μg DNA)	3.8 μL B0015 soln (1 μg DNA)	15 μL phsABC soln (375 ng DNA)
1.8 μL EcoRI & 1.8 μL SpeI	1.8 μL XbaI & 1.8 μL PstI	1.2 μL EcoRI, 1.2 μL PstI, & 1.2 μL DpnI
20.8 μL H2O	37.1 μL H2O	15.9 μL H2O

Wetlab work for this day is also recorded on page 51 of the hard copy lab notebook.
• Thursday 7/8--Further ligation efforts
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Ligation Efforts Continue

• In addition to trying the triple-ligation strategy started on 7/7 (ligation attemp #3) will try trouble-shooting the ligation strategy used in attempts #1 and #2. In particular, will modify digestion protocol and test EcoRI and XbaI (older enzymes) for activity.

Ligation Attempt #3 (Triple Ligation)


• Ran triple ligation all day at room temperature and stored at 4°C. Ligation contents were as follow to have a 1:1:1 stoichiometric ratio of all three components.

Component	Volume
Distilled Water	6.4 μL
T4 Ligase buffer 10x	2 μL
NEB T4 Ligase	1 μL
pSB1C3 solution	2 μL
B0015 solution	2.4 μL
phsABC solution	6.2 μL
Total	20 μL

Ligation Attempt #4


• Concerns about enzyme activity led to reversing the order of the serial digestion of B0015 background so that the first digestion is XbaI (low salt buffer) and the second is EcoRI (high salt buffer). Will also omit the pre-ligation PCR purification step.
• Overnight digestion of ligation components--Set up the following digestions to run overnight at 37°C. The EcoRI was newly purchased as there was concern about the age of the previously used enzyme.

phsABC double digestion
NEB EcoRI Buffer	5 μL
BSA 100x	0.5 μL
phsABC solution	30.8 μL (1 μg DNA)
NEB EcoRI	1.8 μL
NEB SpeI	1.8 μL
Sterile H2O	10.1 μL

B0015 digestion
NEB Buffer 4	5 μL
BSA 100x	0.5 μL
NEB XbaI	3.6 μL
B0015 solution	3.8 μL ( 1 μg DNA)
Sterile H2O	37.1 μL

Wetlab work for this day is also recorded on pages 52 and 53 of the hard copy lab notebook.
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