Team:TU Delft/30 July 2010 content

From 2010.igem.org

(Difference between revisions)
(Alkane Sensing, Solvent Tolerance and Salt Tolerance)
(Alkane Sensing, Solvent Tolerance and Salt Tolerance)
Line 157: Line 157:
|✓
|✓
|‘X–PhPFDalpha–P’
|‘X–PhPFDalpha–P’
 +
|}
 +
 +
==Ligation==
 +
The digestion products were [[Team:TU_Delft/protocols/ligation|ligated]] over two nights:
 +
 +
{| style="color:black; background-color:white;" cellpadding="5" cellspacing="0" border="1"
 +
|'''#'''
 +
|'''BioBrick'''
 +
|'''Fragment 1'''
 +
|'''Fragment 2'''
 +
|'''Final volume'''
 +
|-
 +
|1
 +
|AlkS + E0240
 +
|4 μL ‘E–007–S’
 +
|4 μL ‘X–00–P’
 +
|
 +
|-
 +
|2
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
 +
|-
 +
|3
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
 +
|-
 +
|4
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
 +
|-
 +
|5
 +
|
 +
|? μL ‘E-Part1-S’
 +
|? μL ‘X-Part2-P'
 +
|
 +
|-
 +
|6
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
 +
|-
 +
|7
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
 +
|-
 +
|8
 +
|
 +
|? μL ‘E – Part – S’
 +
|? μL ‘X – Part – P’
 +
|
|}
|}

Revision as of 10:20, 2 August 2010

Contents

Alkane Sensing, Solvent Tolerance and Salt Tolerance

by Pieter

I tried to assemble the remaining biobricks from various sub projects. The goal is to assemble the following:

  • AlkS + E0240
  • PalkB + J06702
  • J61101 + bbc1
  • J61101 + PhPFDalpha
  • J61101 + PhPFDbeta

To achieve this J06702, bbc1, PhPFDalpha and PhPFDbeta were amplified by PCR. The J61101 was cut open with S and P after which the biobricks were inserted. AlkS was inserted in the backbone with E0240.

PCR with PFX

Per sample the following mix was used:

  • 1,5 ul 10 mM dNTPs
  • 5 ul Enhancer
  • 5 ul 10x PFX Buffer
  • 1 ul 50 mM MgSO4
  • 3 ul 5 pmol/ul Forward Primer
  • 3 ul 5 pmol/ul Reverse Primer
  • 0.6 ul PFX Polymerase
  • 1 ul DNA Template
  • 29.9 ul H2O

PCR Program: start:

  • 2 min 95 C
  • 1 min 50 C
  • 1 min 68 C

repeated 25 times:

  • 1 min 95 C
  • 1 min 50 C
  • 1 min 68 C

end:

  • 10 min 68 C

PCR reactions

# Description Expected lenght (bp) Primer Status Remarks
1 Marker n/a n/a n/a
2 J06702 869 G00100 + G00101
3 bbc1 703 MF + MR2
4 PhPFDalpha 528 MF + MR2
5 PhPFDbeta 430 MF + MR2

Digestion

The PCR products were subsequently digested:

# Sample Enzyme 1 Enzyme 2 Buffer BSA Needed fragment
1 2 μL AlkS EcoRI SpeI 2 (BioLabs) ‘E–AlkS–S’
2 3 μL E0240 EcoRI XbaI 2 (BioLabs) ‘X–AlkS–E’
3 16 μL PalkB SpeI PstI 2 (BioLabs) ‘P–PalkB–S’
4 40 μL J06702 PCR product XbaI PstI 2 (BioLabs) ‘X–J06702–P’
5 6 μL J61101 SpeI PstI 2 (BioLabs) ‘P–J61101–S’
6 40 μL bbc1 PCR product XbaI PstI 2 (BioLabs) ‘X–J61101–P’
7 40 μL PhPFDalpha PCR product XbaI PstI 2 (BioLabs) ‘X–PhPFDalpha–P’
8 40 μL PhPFDbeta PCR product XbaI PstI 2 (BioLabs) ‘X–PhPFDalpha–P’

Ligation

The digestion products were ligated over two nights:

# BioBrick Fragment 1 Fragment 2 Final volume
1 AlkS + E0240 4 μL ‘E–007–S’ 4 μL ‘X–00–P’
2 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’
3 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’
4 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’
5 ? μL ‘E-Part1-S’ ? μL ‘X-Part2-P'
6 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’
7 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’
8 ? μL ‘E – Part – S’ ? μL ‘X – Part – P’