Integration of a landing pad brick
Carolyn N Bayer, Maja Rennig, Anja Ehrmann, Morten Norholm
Abstract
SEGA, the Standardized Genome Engineering Architecture, is a comprehensive strain collection that enables genome engineering by combining only two reagents: a DNA fragment that can be ordered from a commercial vendor and a stock solution of bacterial cells followed by incubation on agar plates. Recombinant genomes are identified by visual inspection using green-white colony screening akin to classical blue-white screening for recombinant plasmids. The modular nature of SEGA allows precise multi-level control of transcriptional, translational, and post-translational regulation. The SEGA architecture simultaneously supports increased standardization of genetic designs and a broad application range by utilizing well-characterized parts optimized for robust performance in the context of the bacterial genome
This protocol describes to process of integrating a SEGA landing pad brick. A landing pad brick is integrated using tetA positive selection. This protocol also applies to integration of other bricks using tetA positive selection, e.g. complementation of split tetA .
Before start
Transform a SEGA strain with pSIM19 (Spectinomycin resistance). From now on cultures have to be kept at 30°C to retain the plasmid (temperature-sensitive ori )
Steps
transform your desired SEGA strain with pSIM19 (Spectinomycin resistance). From now on cultures have to be kept at 30°C to retain the plasmid (temperature-sensitive ori )
preculture and DNA fragment- Day 1
Prepare a PCR product of the landing pad brick and purify it from an agarose gel.
Setup a preculture of the strain with pSIM19 in LB medium supplemented with Spectinomycin 0.05mg/mL
250rpm
Recombineering- Day 2
Prepare:
Cold sterile water
Cold Glycerol 15% volume
Pre-chilled centrifuge and tabletop centrifuge to 4°C
LB agar plates supplemented with0.025mg/mL or 0.05mg/mL Tetracycline
Inoculate 50mL LB-Medium supplemented with Spectinomycin (0.05mg/mL) with 500µL of the preculture from step 3
Incubate at 250rpm until cultures reached an OD600 of 0.5
Induce expression by transferring the culture to a shaking water bath at 150rpm
Transfer culture to prechilled 50mL falcon tubes and put on ice for 0h 15m 0s
Spin the culture down at 4000x g,4°C and discard the supernatant
Add 1mL of ice cold water, resuspend and transfer to a 1.5 ml tube
Spin at 11000x g,4°C in a tabletop centrifuge
Wash pellet twice with 1mL ice cold water
Resuspend the pellet in 600µL cold glycerol (15% volume)
Unused cells can be stored at -80°C
Electroporate 50µL of cells with 200ng of purified PCR product from step 2 or 2µL of 100micromolar (µM) single stranded oligonucleotide
Recover cells 800rpm in a tabletop shaker using SOC medium
Plate cells on LB agar plates supplemented with 0.025mg/mL or 0.05mg/mL Tetracycline
Incubate at 30°C for 24h 0m 0s up to 48h 0m 0s
Screening- Day 3-4
Screen for positive colonies by "green-white screening"on a blue-light table and perform colony PCR on the fluorescent colonies to identify the correct recombinants
