Team:Yale/Our Project/Notebook/Week 4

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lab notebook: week 4 (6/28 -7/4)

• Monday 6/28--PCR amplification of thiosulfate reductase operon phsABC
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pSB74 transformants
Extensive colony growth was seen on plated transformations of pSB74 into DH5alpha and LE392 from 6/25 but none was visible on BL21 plate. Continued failure of BL21 transformation suggests that the homemade competent BL21 cells being used are somehow faulty.

PCR amplification of phsABC
• Prior to PCR, took aliquots of all primer samples and diluted them first to 100 uM as detailed below by the chart and then again to 10 uM

Primer	phsABC_F	phsABC_R	phsAB_R	phsC_F
Initial Amount	38.56 nm	46.58 nm	29.03 nm	21.94 nm
Volume of water	385.6 uL	465.8 uL	290.3 uL	219.4 uL

• Similarly, diluted the DNA sample to 10 ng DNA/uL. Started with 0.5 uL of miniprepped pSB74 (sample a) at 67.3 ng/uL and added 2.865 uL of water to get the desired concentration.
PCR reaction

• Added the following to each of three PCR tubes: 10 uL 5x Phusion HF buffer, 27.5 uL water, and 1 uL of dNTPs. 5 uL were added of both the forward and reverse primers (at 10 uM), as was 1 uL of the template DNA. The matching of tube numbers, template DNA, and primers was as follows:

Tube #	2	3	4
Template DNA	phsC	phsAB	phsABC
Primers	phsC_F & phsC_R	phsABC_F & phsAB_R	phsABC_F & phsC_R

• Chilled tubes on ice, then added 0.5 uL of Phusion DNA polymerase and put in thermocycler.
• Prior to designing thermocycler protocol, used oligocalc to get the following Tm values for the primers.

Primer	phsABC_R	phsABC_F	phsAB_R	phsC_F
Tm	73˚C	66˚C	64˚C	72˚C

However, these values seem excessively high, so will just start out with an annealing temperature of 55˚C. Devised the following "phs" Thermocycler Protocol
1. Initial Denaturation-- 2 minutes at 98˚C
2. Denaturation--15 seconds at 98˚C
3. Annealing--15 seconds at 55˚C
4. Extension--3 minutes at 72˚C
Steps 2-4 are repeated for 25 cycles 5. Final Extension--10 minutes at 72˚C
6. Hold--indefinitely at 4˚C
Gel of PCR Products
Ran PCR products on an 0.8% agarose gel with 10 uL of ethidium bromide. Loaded 1 uL of each sample with 9 uL of water and 2 uL of loading buffer. Ran gel until done at 60 V, but had difficulty imaging so left aside to deal visualize the next day, unaware that it would spread.

This day's labwork is also recorded on pages 23-28 of the hard copy lab notebook
• Tuesday 6/29--Gel extraction of PCR amplified phs, TSI agar slant assay for hydrogen sulfide production, & pre-ligation double digestion
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PCR amplification of phs

Because the gel run the previous day was no longer good, had to run a second 0.8% agarose gel of the PCR products to determine the success of the PCR reaction. Below is the image of the gel, with a 1 kb ladder in the leftmost lane, phsC in next lane, phsAB in lane 3, and phsABC in lane 4.

The phsC fragment seems to have been amplified with decent success, but phsABC and phAB are only present in trace amounts, so the thermocycler protocol will have to be tweaked.


In the mean time, gel extract the phsC from lane 2 and the phsABC from lane 4 using the microcentrifuge variant of the standard gel extraction protocol

TSI Agar Slant Assay

Want to confirm that IPTG will induce H₂S production in pSB74 transformants, so inoculate 5 mL Amp/LB liquid cultures of DH5alpha and LE392 transformed with pSB74 and grow them up on shaker at 37˚C for use in TSI agar assay.

The slants don't contain IPTG, so must inject IPTG with the transformants into the slants. Took 200 uL of each cell solution and added to it 50 uL of 1 M IPTG, then injected the resulting mixture into a slant. Left the slants to sit overnight in the fume hood

Double digestion in preparation for ligation

In order to create the desired Biobricks, must insert the phsABC operon into terminator B0015 and put the constitutive promoter J23114 into the generator P0312. Following the Biobrick combination protocol, we then must digest phsABC and J23114 with EcoRI and SpeI and digest B0015 and P0312 with EcoRI and XbaI. The former can be done as a double digest, but the latter must be done sequentially because the enzymes require different buffers.
Set up the following 50 uL digestions:
Digest of phsABC--5 uL EcoRI buffer, 0.5 uL 100x BSA, 40 uL phsABC fragment (from gel extraction), 1.8 uL EcoRI, 1.8 uL SpeI, 0.9 uL water
Digest of J23114--5 uL EcoRI buffer, 0.5 uL 100x BSA, 8 uL miniprepped J23114 (1 ug DNA), 1.8 uL EcoRI , 1.8 uL SpeI, 32.9 uL water
Digest of B0015--5 uL EcoRI buffer, 12 uL miniprepped B0015 (1 ug DNA), 3.6 uL EcoRI , 29.4 uL water
Digest of P0312--5 uL EcoRI buffer, 9 uL miniprepped P0312 (1 ug DNA), 3.6 uL EcoRI , 32.4 uL water

Let each digestion run for two hours at 37˚C, then ran the result through the microcentrifuge version of the PCR purification protocol.
This day's labwork is also recorded on pages 28-31 of the hard copy lab notebook
• Wednesday 6/30--Troubleshooting PCR amplification of thiosulfate reductase gene & continued work toward ligation
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TSI Agar slant

• No visible color change, and decide that it is safe to accelerate growth by moving slants to the 37˚C incubator as research fails to turn up any safety concerns regarding the hydrogen sulfide emitted in this kind of assay.
PCR efforts continue

• Redid 6/29 PCR of phsABC and phsAB, but this time ran two trials of each, with and without 3% DMSO, and changed the thermocycler protocol so that the annealing temperature was 50˚C rather than 55˚C, calling the new protocol "phs50."
• After running the protocol, found that PCR tubes had popped open and contents had evaporated, so set up PCR a second time to run overnight.
Vector digestion & 1st ligation attempt
• Ran the second portion of the B0015 and P0312 sequential digests, with reaction contents of each as follows: 5 uL NEB Buffer 4, 0.5 uL 100x BSA, 3.6 uL XbaI, 40 uL DNA from PCR purification protocol, and 0.9 uL water. Let the reactions run for 2.5 hours at 37˚, but after 1.5 hours added to each reaction 1 uL of Calf Intestinal Phosphatase (CIP) to cleave terminal phosphates and discourage self-ligation in the next step.
Ligation of phsABC and B0015
By this point the DNA concentrations of the digestion reactions are dismally low (around 2 ng/uL for B0015 and phsABC), but will try a ligation anyways while at the same time preparing for a possible redo. Set up digestion reactions of two sizes, 10 uL and 20 uL, with a control reaction for each in which there is no insert.
Reaction 1--small control 1 uL ligase buffer, 0.5 uL T4 ligase, 4.25 uL B0015, 4.25 uL water
Reaction 2--small 1:1 insert:vector1 uL ligase buffer, 0.5 uL T4 ligase, 4.25 uL B0015, 4.25 uL phsABC
Reaction 3--small 2:1 insert:vector1 uL ligase buffer, 0.5 uL T4 ligase, 2.5 uL B0015, 6 uL phsABC
Reaction 4--large control2 uL ligase buffer, 1 uL T4 ligase, 8.5 uL B0015, 8.5 uL water
Reaction 5--large 1:1 insert:vector2 uL ligase buffer, 1 uL T4 ligase, 8.5 uL B0015, 8.5 uL phsABC
Insert to vector ratios are rough and based on the fact that the two are at similar concentrations and are of similar sizes.
Each reaction was let to run 20 minutes at room temperature before being transformed into Xl1-Blue cells according to the standard transformation protocol and then plated on ampicillin LB plates and let to grow overnight.

Cultures for miniprep & glycerol stock redo
In preparation for potential ligation failure, once again inoculated liquid cultures of Amp LB for miniprep with pSB74,P0312,R0011, B0015, and J23114 transformants, making two 5 mL cultures for each plasmid. When OD reached 0.6, once again made glycerol stocks from 0.5 mL of each solution and 0.5 mL of filter-sterilized 50% glycerol. This time flash-froze the stocks immediately, rather than waiting overnight as on
This day's labwork is also recorded on pages 32-36 of the hard copy lab notebook.
• Thursday 7/1--Smelly bacteria (yay!) & ongoing ligation efforts
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TSI agar assay

• LE392 and DH5alpha cultures in TSI agar showed some growth. No black color change was visible, but both slants had a rotten egg scent, so suspected generation of H₂S at concentrations too low to visibly trigger color change yet.



PCR work

• Ran 1.0% agarose gel of four 6/30 PCR products at 90 V.
Gel of phsABC and phsAB PCR products or a demonstration of the utility of DMSO Lane 1: 1 kb ladder and 3.6 kb spillover from Lane 2, Lane 2: 3.6 kb phsABC fragment from PCR protocol without DMSO, Lane 4: 2.9 kb phsAB fragment from PCR protocol without DMSO, Lane 6:3.6 kb phsABC fragment from PCR protocol with DMSO, Lane 8: 2.9 kb phsAB fragment from PCR protocol with DMSO Gel of phsABC and phsAB PCR products or a demonstration of the utility of DMSO Lane 1: 1 kb ladder and 3.6 kb spillover from Lane 2, Lane 2: 3.6 kb phsABC fragment from PCR protocol without DMSO, Lane 4: 2.9 kb phsAB fragment from PCR protocol without DMSO, Lane 6:3.6 kb phsABC fragment from PCR protocol with DMSO, Lane 8: 2.9 kb phsAB fragment from PCR protocol with DMSO

• Based on gel, it appears that the phs50 thermocycler protocol is an improvement from phs protocol and that including DMSO also improves yield
• Cut out largest band for each lane and ran through standard gel extraction protocol.

Stockpiling plasmids for later


• Miniprepped LE392 cultures grown overnight,resulting in two Eppendorfs apiece of the following plasmids: B0015 (double terminator), J23114 (constitutive promoter), pSB74 (thiosulfate reductase), R0011 (IPTG-inducible promoter), and P0312 (lacI needed with R0011). Nanodropping gave the following concentrations:



Sample	B0015-1	B0015-2	P0312-1	P0312-1	J23114-1	J23114-2	pSB74-1	pSB74-2	R0011-1	R0011-2
Concentration (ng DNA/uL)	262.3	28569	129.1	92.3	189.0	202.6	214.4	284.4	102.6	79.6

Results of 6/30 Ligation (Ligation Attempt #1)

• Plated post-ligation transformants showed the following results:
Reaction #1 (small control) 0 colonies
Reaction #2 (1:1 insert:vector) 2 colonies, numbered 1A and 2A
Reaction #3 (2:1 insert:vector) 0 colonies
Reaction #4 (large control) 2 colonies
Reaction #5 (large 1:1 insert vector) 2 colonies, numbered 3A and 4A
Concerned about the small number of colonies and low ratio of number of colonies from actual ligation to number of colonies from control ligation.

• Started liquid cultures and index plates of four colonies from reactions 2 and 5.
• Also set up colony PCR for all four colonies, spotting the template DNA into tubes with the following contents and running on thermocycler protocol phs50

Component	Volume
Distilled Water	27 μL
Phusion 5x Buffer	10 μL
DMSO	1.5 μL
10 mM dNTPs	1 μL
10 uM phsABC_F primer	5 μL
10 uM phsABC_R primer	5 μL
Phusion Polymerase	0.5 μL
Template DNA	spotting
Total	50 μL

• After PCR, ran 1.0% agarose gel of colony PCR reaction solutions at 90 V versus a 1 kb ladder. A preliminary visualization showed no visible non-primer DNA except for a band between 3 and 4 kb for the PCR product from colony 1. Based on a later visualization said band appeared to be closer to 3 kb, suggesting the 3.2 kb B0015 vector rather than the 3.6 kb insert. Unfortunately gel was dropped and damaged irreparably before picture could actually be taken.

Wetlab work for this day is also described on pages 37-41 of the hard copy lab notebook
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