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Revision as of 03:28, 7 October 2016
JOURNAL
CDI
Protein Cages
1
Construction of ATCC 13048 Loci 2 in pSB1C3
Isolation of template DNA from EC93, EC869, and ATCC 13048; PCR of Gibson fragments for EBL1 and EBL2 in pSB1C3 construct
27
Inoculation of strains obtained from Dr. Christopher Hayes
Inoculated overnight cultures of:
- EPI100 w/ EC869 cosmid
- X90 w/ EC93 cosmid
- ATCC 13048
Conditions:
- 10mL LB
- 10uL ampicillin
- 37 C for 16h shaking
28
Isolation of template DNA
Miniprep of EC93 and EC869
- EC93 #1: 145.42 ng/μL
- EC93 #2: 198.85 ng/μL
- EC869 #1: 90.81 ng/μL
- EC869 #2: 45.95 ng/μL
gDNA isolation of ATCC 13048
- 34.87 ng/μL
Gibson primers designed for EBL1 and EBL2 toxin switched constructs in pSB1C3 and pSC101
29
PCR of Gibson fragments for EBL1 and EBL2 in pSB1C3
50uL rxn:
- 2.5 uL F primer
- 2.5 uL R primer
- 25 uL Q5 2X MM
- 19 uL dH2O
Fragments:
- EBL1 in pSB1C3 frag 2
- EBL2 in pSB1C3 frag 2
- EBL2 in pSB1C3 frag 3
Cycling conditions:
- 98C -- 30s
- 98C -- 10s
- TmC -- 30s
- 72C -- ext time
- 72C -- 2min
28 cycles
30
Troubleshooting PCR of Gibson fragments
- try using KAPA Hifi instead of Q5
- add more template gDNA (1ng, 10ng, 35ng, 70ng)
- 0.75 uL F primer
- 0.75 uL R primer
- 12.5 uL KAPA Hifi 2X MM
- dH2O up to 25 uL
- EBL1 in pSB1C3 frag 2 (Tm = 66C, ext time = 140s)
- EBL2 in pSB1C3 frag 2 (Tm = 65C, ext time = 88s)
- EBL2 in pSB1C3 frag 3 (Tm = 65C, ext time = 180s)
- 98C -- 30s
- 98C -- 10s
- TmC -- 30s
- 72C -- ext time
- 72C -- 2min
25uL rxn:
Fragments:
Cycling conditions:
28 cycles
ladder; EBL2 frag 2; EBL1 frag 2; EBL2 frag 3
2
Construction of ATCC 13048 Loci 2 in pSB1C3 Cont.
PCR of Gibson fragments for EBL1 and EBL2 in pSB1C3 construct
5
PCR of EBL1 and EBL2 Gibson fragments for pSB1C3
- EBL1 in pSB1C3 frag 2 (Tm = 66C, ext time = 210s)
- EBL2 in pSB1C3 frag 1 (Tm = 65C, ext time = 180s)
- EBL2 in pSB1C3 frag 4 (Tm = 64C, ext time = 120s)
- 98C -- 30s
- 98C -- 10s
- Tm -- 30s
- 72C -- ext time
- 72C -- 2min
- 14C -- infinite
- only primer dimers observed
Redoing failed PCR, modified protocol by having elongation time be extended to be 30s/kb; annealing temperature set to 72C; ran 25uL and 50uL rxn
Fragments:
Cycling conditions:
28 cycles
ladder; EBL2 frag 1; EBL2 frag 4; EBL1 frag 2 (25uL); EBL1 frag 2 (50uL)
6
Troubleshooting PCR of EBL1 frag 2, EBL2 frag 1, EBL2 frag 4
- cycling conditions remained constant
- doubling template DNA resolved EBL2 frag 2 and 4 problem; most likely faulty primers for EBL1 frag 2
Redoing failed PCR, modified protocol by doubling and quadrupling template dna amount; changed from 28 to 32 cycles
ladder; 2x EBL1 frag 2; 4x EBL1 frag 2; 2x EBL1 frag 1; 4 EBL1 frag 1; 2x EBL1 frag 4; 4x EBL1 frag 4
7
Transformation of DH5-alpha with EC93 cosmid and pSK33
8
Troubleshooting PCR of EBL1 frag 2 in pSB1C3 Cont.
inoculated starter cultures of DH5-alpha w/ EC93, DH5-alpha w/ pSK33, and X90 w/ EC93
9
Verification of EC93 cosmid and miniprepping for more pSK33
ran test digest to confirm EC93 cosmid:
- 500 ng DNA
- 5uL NEB 2.1
- 1uL EcoRI
- H2O to 50uL
expecting bands at 10kb and 8kb
ladder;EC93 cosmid from DH5-alpha;EC93 cosmid from X90;ladder