Team:Wageningen UR/Journal/week12

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(→week 12: 16 july - 22 july)
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From the transformation plate of week 9 a new colony was grown and subsequently a miniprep was done. The yield was about 160 ng/µl. To check if the transformed E.coli contains the right plasmid a digestion check with the restriction enzymes BamHI and BgEII was done.
From the transformation plate of week 9 a new colony was grown and subsequently a miniprep was done. The yield was about 160 ng/µl. To check if the transformed E.coli contains the right plasmid a digestion check with the restriction enzymes BamHI and BgEII was done.
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''' CCMV '''
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18-07 First PCR on CCMV-Delta26 to create the CCMV_NEG construct.
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Phusion Mastermix for 4 + 1 = 5 samples:
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H2O 176.25 uL
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5x Phusion Buffer 50 uL
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dNTP’s 5 uL
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Phusion Enzyme 1.25 uL
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Total 232.5 uL
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Preparation samples:
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Mastermix 44 uL
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DNA Template 1 uL
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Forward Primer (10x diluted) 2.5 uL
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Reverse Primer (10x diluted) 2.5 uL
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Total 50 uL
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PCR reaction:
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Step 1: 10 minutes at 98 °C
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Step 2: 30 seconds at 98 °C
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Step 3: 30 seconds at 58 °C
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Step 4: 30 seconds at 72 °C --> step 2 (35 times)
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Step 5: 10 minutes at 72 °C
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Step 6: Keep at 4 °C
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Lane 1: Marker
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Lane 2: Negative control: No template, same primers as duplo’s
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Lane 3: Positive control: Delta26-Histag CCMV with Forward + Reverse (suffix) primer.
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Lane 4 & 5: 2 duplo’s: CCMV-Delta26 with Forward (Part 2) + Reverse (suffix) primer.
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[[File:Gel 18-07.tif|200px|center|thumb|<p align="justify">Figure 1: 1% agarose gel </p>]]

Revision as of 15:19, 24 September 2012

week 12: 16 july - 22 july

Office work

PLRV

This week we designed and ordered all the primers we needed.

Primers.jpg

Lab work

General

BBa_J04450 (RFP coding device) transformation, digestion check

  • BBa_J04450 was solubilized from the Standard registry parts plate I with 10µl MQ water
  • Transformation of electrocompetent E.coli with the plasmid
  • Plated on LB-agar with corresponding antibiotic (chloramphenicol)
  • 6 red-fluorescing colony were picked after overnight growth in 37°C
  • Subsequent miniprep
sample concentration (ng/µl) 260/280
A1 115.5 1.92
C1 96.0 1.98
C3 100.1 1.92
  • Digestion check with EcoRI and SpeI

Digestion of BBa_K1970- 22/38

From the transformation plate of week 9 a new colony was grown and subsequently a miniprep was done. The yield was about 160 ng/µl. To check if the transformed E.coli contains the right plasmid a digestion check with the restriction enzymes BamHI and BgEII was done.


CCMV

18-07 First PCR on CCMV-Delta26 to create the CCMV_NEG construct.

Phusion Mastermix for 4 + 1 = 5 samples:

H2O 176.25 uL 5x Phusion Buffer 50 uL dNTP’s 5 uL Phusion Enzyme 1.25 uL Total 232.5 uL


Preparation samples:

Mastermix 44 uL DNA Template 1 uL Forward Primer (10x diluted) 2.5 uL Reverse Primer (10x diluted) 2.5 uL Total 50 uL

PCR reaction:

Step 1: 10 minutes at 98 °C Step 2: 30 seconds at 98 °C Step 3: 30 seconds at 58 °C Step 4: 30 seconds at 72 °C --> step 2 (35 times) Step 5: 10 minutes at 72 °C Step 6: Keep at 4 °C

Lane 1: Marker Lane 2: Negative control: No template, same primers as duplo’s Lane 3: Positive control: Delta26-Histag CCMV with Forward + Reverse (suffix) primer. Lane 4 & 5: 2 duplo’s: CCMV-Delta26 with Forward (Part 2) + Reverse (suffix) primer.

File:Gel 18-07.tif


HepB

  • Digestion of the HepB core protein PCR product with pre- and suffix (from 11.July) and ligation into BBa_J04500 (an IPTG inducible promoter with RBS)as well as BBa_PSB1K3.ml (linearized plasmid backbone)
  • Electro transformation of these constructs with DH5α
  • Colony PCR (20 samples of the transformants containing HepB core protein + BBa_J04500; 10 samples of the transformants containing HepB core protein + BBa_PSB1K3.ml

-> The ligation and transformation of the HepB core protein into the linear backbone (BBa_PSB1K3.ml) was not successful -> The colony PCR shows that we have 6 out of 20 colonies with the expected insert size (around 600bp)


Figure 1: Colony PCR 20 July - HepB in BBa_J04500



TuYV

  • Mach1 electrocompetent E. coli cells were transformed with last week's ligation mixtures (TuYV coat protein and TuYV coat protein with his-tag). Results were unsatisfying. No colonies were showed on the sample plates.
  • 'Coat Protein + readthrough' gene amplicons were digested, ligated into pSB1K3 backbone and transformed into our electrocompetent Mach1 E. coli cells. After two attempts and a colony PCR, results were still unsatisfying.


PLRV

After a two week quest for PLRV infected plant material, we obtained infected potato leafs from the Dutch General Inspection Service for Agricultural seed and seed potatoes.

DLS boundary experiment


19th July (Mark)

  • DLS measurment: 20 runs, 45 seconds
    • Changed 4 times to different vials to see if the vials are important to the measurment


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