Difference between revisions of "Part:BBa K1616005:Experience"

Revision as of 00:19, 23 September 2015

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Applications of BBa_K1616005

Notebook

Gblocks: ordered of Holin/ Endolysin fragments from IDT

PCR of Holin/Endolysin parts

Aim: Amplification of the part

	MQ Water	RB Buffer	Mg²⁺	dNTP 10 µM	Primer Fwd 25 µM	Primer Rev 25 µ	DNA	Taq Pol enzyme
Holin - Ensolysin	39 µL	5 µL	1,5 µL	1 µL	1µL pSB1C3 Fwd	1µL pSB1C3 Rev	1 µL	0,5 µL

Ligation of Gblocks Holin-Endolysin into pDawn

Tube	Water	T4 ligase Buffer	pDawn	Plasmid	T4 ligase
Holin - Ensolysin	4,6 µL	1 µL	1,4 µL	2,5 µL	0,5 µL

Room temperature, 30min heat kill: 80°C, 20min

Transformation of E.coli DH5 alpha competent cells

Culture liquid: pDawn – H/E 20 mL LB + 20 µL Kan, without light;

Results

Bacteria expressing pDawn-HE were prepared in a pre-culture until DO600 reached a value between 0,6 and 0,8. Then, one condition was illuminated with white-light and incubated at 37°C, another one was kept in the dark and incubated at 37°C and the last condition was illuminated with white-light and incubated at room temperature. The value of DO was taken regularly to observe the kinetic of growth under each condition.

In absence of light, and at 37°C, bacteria growth was normal but light illumination was enough to slow-down the growth of bacteria. Incubation at room temperature with white-light illumination allowed better folding of HE and had a stronger effect on the growth of bacteria.

User Reviews

UNIQ41edf72011d1a440-partinfo-00000000-QINU UNIQ41edf72011d1a440-partinfo-00000001-QINU

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