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From 2014.igem.org

Contents 1 Week 1 2 Week 2 3 Week 3 4 Week 4

Week 1

Notes: Unless stated otherwise, all gels contain 2-log ladder

5/9

• •Obtained BW23115 KanR cells- BW23115 cells that had their native CRISPR-Cas system knocked out by the insertion of a Kanamycin resistance gene
  • -Will also be called BW23115 or BW
  • -Conjugated BW23115 KanR cells with contain F’ notation (ex. BWF’)
• •Obtained ER2738 cells that contain the F’ episome (no changes from NEB sample)
  • -Will also be called ER. Assume that all ER samples contain the F’ episome
  • -Streaked sample onto LB+Tet (20ug/mL) to select for colonies containing F’ episome

5/10

• •Did receive colonies from 5/9 selection

Week 2

5/12

• •Need to conjugate BW23115 KanR cells with the F’ episome
  • -Set up overnight cultures of ER2738 and BW23115 KanR
  • -When mixed, ER2738 will donate it’s F’ episome and BW23115 KanR will receive the F’ episome. F’ episome confers Tetracycline resistance

5/13

• •Started M13 Amplification: Amplify M13 phage using the M13K07 Helper Phage
  • -Let precipitated in NaCl/PEG solution overnight
  • -Possible sources of error

Did not sterilize 2.5M NaCl/20% PEG-8000 solution

Added 4-fold PEG solution

• • • • •Compensated by adding more LB

During precipitation, put sample in -20C for 30 minutes before realizing mistake and moving to it to 4C. Sample partially froze

• •Conjugated BW23115 with F’ episome
  • -Added 1mL BW23115 to 1mL ER2738 overnight culture
  • -Incubated at 37C for 30 minutes, shaking
  • -Plated on LB+Kan(50ug/mL)+Tet(20ug/mL)

To select for BW cells that took the F’ episome (containing Tet resistance)

5/14

• •Finished the M13 Amplification
  • -Visualized product on UV-vis. There was a tall spike at 269nm indicating that DNA was present. Did not test at 320nm.
• •Results of BW23115 Conjugation
  • -Many colonies indicating successful conjugation of F’ episome into BW23115
  • -Set up overnight to make freeze down tomorrow
• •Set up overnight of ER2738 to make chemically competent tomorrow

5/15

• •Made freeze down of BW23115 KanR F’
  • -BW23115 E. coli strain with Kanamycin resistance gene inserted into genome and with F’ episome
• •Made chemically competent ER2738 cells
• •Transformation of Litmus28i (from NEB) into chemically competent ER2738 cells
  • -Added 1ul Litmus28i plasmid to 40ul competent cells
  • -Plated on LB + Amp(100ug/mL)
  • -Purpose: To make M13 phage that package Litmus28i DNA. Need phagemid (Litmus28i) DNA in infectable cells (cells containing F’ episome) to introduce M13K07 Helper Phage and make phage.

5/16

• •Results of 5/15 transformation
  • -No growth for No DNA control
  • -Many colonies for sample

Week 3

5/19

• •M13 Amplification to isolate M13-Litmus28i phage
  • -Cells: ER2738 cells containing Litmus28i phagemid
  • -Helper Phage: M13K07
  • -Not much phage was precipitated
• •Set up overnight culture of ER2738 to infect tomorrow

5/20

• •Infected ER2738 cells with M13-Litmus28i phage
  • -Plated only on Ampicillin(100ug/mL) (should have also plated on kanamycin)
  • -Infected for 4-5 hours-> should have only infected for 30 minutes maximum. This extra time gives the cells that were infected with M13-M13K07 the time to produced M13-M13K07 phage and reinfect

5/21

• •Results from M13-Litmus28i infection of ER2738
  • -Solid lawn of growth for diluted and non-diluted
  • -Also sickly looking growth
• •Set up overnights
  • -ER2738 cells containing Litmus28i for freeze down
  • -BW23115 with F’ episome to make chemically competent cells
  • -ER2738 to redo infection

5/22

• •Tested absorbance of phage produced through M13 amplification on 5/19
  • -Low absorbance of 0.018 at 269nm but no detection at wavelength 320nm
  • -Decided to redo M13 amplification
• •Made chemically competent BW23115 with f-episome
• •Made freeze down of ER2738 containing Litmus28i
• •Set up overnight of ER2738 containing Litmus28i to redo M13 amplification tomorrow

5/23

• •Protocol switch to make phage using phagemid
  • -“M13 Amplification” protocol should only be used to make more M13-M13K07, not to make M13 phage containing a different phagemid
  • -Switched to new protocol (“Use of M13K07 Helper Phage for isolation of single stranded phagemid DNA” by NEB. Made modifications (see our protocols) to isolate phage rather than single-stranded DNA)
  • -Making phage….

DATA TABLE HERE******************************************

• •Made fresh antibiotics
  • -Chloramphenicol (34 ng/mL)

1.44g chloramphenicol into 42mL EtOH

• • -Ampicillin (50 ng/mL)

4g ampicillin into 80mL mili-Q H2O

5/24

• •Isolated phage using new protocol
  • -Resuspended pellet in 200ul TBS and 200ul 30% glycerol
  • -Measured absorbance with UV-vis

concentration (phage/mL) = 6x10^16 x (A269-A320)/ (#of base pairs in the phage genome)

DATA TABLE HERE************************************************

• •Infect ER2738 cells with M13-Litmus28i
  • -Wanted 1:10 phage:cell ratio. Math….

At 1 OD (e.coli), cell/mL = 5x10^8

5x10^7 phage * (1mL/4.72x10^12 phage) = 0.011ul phage

• •Set up overnights
  • -ER2738 for infection with M13-Litmus28i
  • -BW23115 F’ for infection with M13-Litmus28i to test infectivity of conjugated strain

Week 4

5/25

• •Infect ER and BWF’ cells with M13-Litmus28i
  • -Made 5mL culture of ER and BW that was at 1 OD

DATA TABLE HERE********************************************************

• • -Based on calculations from 5/24, we needed to add 0.011 ul phage per 1 mL of cells at 1 OD. This equates to 0.055 ul of phage into 5 mL cells; therefore we made a 1:10 dilution so we could add 0.5ul. Unfortunately, the pipet would not take up 0.5ul so we added 0.8ul of M13-Litmus28i phage
  • -Grew the cells for 20 minutes at 37C
  • -Plated 300ul onto Kanamycin (50ug/mL) and 300ul onto Ampicillin (100ug/mL) for each sample

Incubated overnight at 37C

• •Note: During the production of phage, the phagemid SHOULD be packaged preferentially over the Helper Phagemid but some Helper Phagemid will still be packaged. We plated on Amp to select for cells that were infected with phage containing Phagemid. We plated on Kan to select for cells that were infected with phage containing Helper Phagemid. This allows us to compare the packaging efficiency of Helper Phagemid: Phagemid.

5/26

• •Results from 5/25 infection with M13-Litmus28i

DATA TABLE HERE***********************************

• • -Conclusions:

Cells grew on Ampicillin; therefore, Litmus28i phagemid was successfully packaged into M13 phage.

For ER2738 samples, there was significant growth on Ampicillin compared to Kanamycin; therefore, Litmus28i phagemid is packaged preferentially over M13K07 Helper Phagemid

M13-Litmus28i retains its infectivity of cells containing the F’ episome

• • -Because we received lawns, we have to redo the infection and plate less cells so we can calculate the uptake ratio between the phagemid and helper phage based on the number of colonies
• •Started 50 mL overnight of K12 ER2738 and BW23115

5/27

• •Redo the infection done on 5/25
  • -Infectable cells: ER2738 and BW23115

Plated non-infected samples of each (non-diluted) to check for contaminants

• • -Diluted M13-Litmus28i (1) phage by a factor of 10. Added 5.5ul to each sample
  • -Grew samples for 20 minutes at 37C, 250rpm
  • -Plated 100ul of onto an Ampicillin (100ug/mL) plate and onto a Kanamycin (50ug/mL) plate. Incubated overnight at 37C.

Dilutions = 1:10; 1:100; and 1:1000

5/28

• •Results from 5/27
  • -Controls were as expected

No growth for ER2738 non-infected grown on Amp, ER2738 non-infected grown on Kan, or BW23115 non-infected grown on Amp

Growth for BW23115 non-infected grown on Kan (BW23115 has Kan R in genome)

• • -Many colonies were received for all dilutions (1:10, 1:100, and 1:1000) of the following

ER2738 infected and plated on Amp

BW23115 infected and plated on Amp

BW23115 infected and plated on Kan

• • -Many (100s to 1000?) colonies grew on 1:10 and 1:100 dilutions of ER2738. 50-100 colonies grew on the 1:1000 dilution of ER2738

Compare this to the 100-200 colonies that grew from 2/25 infection (which was 300ul non-diluted, infected cells)

Reasons for increased yield

• •Added too much phage?
• •volume changed between experiment (5mL to 50mL)
• •Overnight culture may not have been saturated. If still in log phase, the cells would continue to grow
• •Made 50mL O/N cultures of ER2738 and BW23115 so we can repeat the infection tomorrow and plate further dilutions starting at 1:1000
  • -Carry out infection in 5mL and 50mL to test volume effect?

5/29

• •Measured OD of overnights

DATA TABLE HERE**************************************************

• •Experiment 1: Infect cells using same method as 5/25 (in a 5mL culture)
  • -Started with 1OD cells in 5mL
  • -Added about 0.7ul (inaccuracies in pipet) of 1:10 diluted M13-Litmus28i phage
  • -Incubated (rotating) for 20 minutes
  • -Made 1:1,000 and 1:10,000 dilutions
  • -Plated 100ul on Ampicillin (100ug/mL) plates and on Kanamycin (50ugmL) plates

Included non-infected samples diluted by 1:1000

This negative control can be used for Experiment 2 since the non-infected parent solution is the same

• • -Incubate overnight at 37C
• •Experiment 2: Infect cells using protocol from “Eliminating helper phage from phage display”
  • -Diluted O/Ns to OD of 0.1 in 50 mL culture
  • -Grew samples until of OD of ER2728 = 0.59 and the OD of BW23115 = 0.60

Missed OD of 0.5 mark, but the two samples are close to each other

• • -Chilled samples on ice for 30 minutes
  • -Warmed in incubator for 35 minutes (should have been 30)
  • -Amount of phage. Rather than use 1:1 as mentioned in protocol, we used multiplicity of 1:10 (phage:cell)

Added 3.3ul of 1:10 diluted M13-Litmus28i (1) phage

•(On 5/27 we added 5.5ul of diluted phage to 50mL of cells at OD of 1. Our cells were at OD of .6; therefore, 5.5*.6 = 3.3ul)

• • -Incubated for 30 minutes at 37C, not shaking

We later change this to shaking

• • -Dilutions

1:1,000; 1:5,000; 1:10,000; 1:50,000; 1:100,000; 1:1,000,000

Plated ER2738 and BW23115 on Ampicillin (100ug/mL)

Plated ER2738 on Kanamycin (50ug/mL)

• •Experiment 3: Growth Test (for growth curve)
  • -We were concerned by the low OD of the Overnights from the last few days. Wanted to be sure that 2.0-3.0 was not still in log phase. Cultures looked saturated but the OD seemed low.

DATA TABLE HERE ****************************************

47 (369 minutes elapsed) for BW23115 conjugated (without antibiotics) is most likely an error. It has been removed from the growth plot

GRAPH HERE *****************************************************