Difference between revisions of "Part:BBa K4229046"

Revision as of 07:32, 12 October 2022

Assembly of "minimal wiffelball" under regulation of lambdapLhybrid promotor and LacI promotor

This Biobrick shows the minimal wiffleball without any of the tags. Here the two minimal wiffleballs will be compared. For the minimalwiffle with tags search: BBa_K4229047. The full wiffleball withouttags: BBa_K4229048. The full wiffleball with the tags: BBa_K4229049. We used fluorescent microscopy to monitor the uptake of fluorescent proteins linked with the Spy and Snoop-catcher into the wiffleballs. The Spy-Catcher is fused to the fluorescent protein mVenus2 and the Snoop-Catcher to mTurquoise2 [Fig.1]. We expected that the uptake of the fluorescent proteins into the compartments should alter the fluorescence distribution in the cells, as most of the fluorescent protein is expected to be recruited into the microcompartment. The microscopy was done with a Zeiss Axiovert with Colibri-LEDs. Complementing our microscopy, we conducted western blots to assess the amount of caught protein bound to the wiffleball subunit BMC T1. Successful catching results in a shift of the bands upwards, due to the change of their molecular weight. For the detection of T1 an anti-His antibody was used against the His-tag of the T1. Furthermore, an antibody against the beta-subunit an antibody against the beta-subunit of the E. coli RNAPolymerase was used a loading control. Both primary antibodies were detected with an anti-mouse-horseradish peroxidase (HRP) conjugate, which was detected with ECL-solution . We used the same induced BL21 cells for the microscopy and the western blot. After an induction test, we decided to use 100µM IPTG for wiffleball induction and 50ng/µl doxycycline for the fluorescent protein expression (mVenus2 or mTurquoise2). The bacteria were grown in overnight cultures shaken at 30°C, 200rpm, induced at OD600= 0.6-0.7. Samples were taken after 24h of incubation at 200 rpm at 18°C. Conditions were based on literature research. In general, culture, induction and expression conditions are highly sensitive for microcompartments since they tend to form insoluble aggregates. We also fractioned the cell lysate to observe the solubility of the wiffleballs. All experiments were repeated a total of three times, with the exception of the Snoop-catching experiments. These were just performed two times.

[Fig.1]Principle of catching proteins via Spy/Snp-Catcher by T1 and their incorporation into the BMCs, illustrated as an example of incorporating mVenus2 in the full wiffleball

We expressed tagged mVenus2 either alone or co-expressed with the wiffleballs, which were either tagged or not tagged with the Spy/Snoop-tag at the T1 protein. The results gave us important insights: samples with tagless wiffleballs show an evenly distributed fluorescence [Fig.2:A]. On the other hand, the T1 with tags resulted in fluorescent foci in some cells standing out of the fluorescent background [Fig.2B arrows]. The foci in the full wiffleball were always found at one or both poles of the cells. The minimal wiffleball had fewer and smaller foci, which were also localized in other areas of the bacteria. The foci were easier detectable in less fluorescent cells. Therefore, more foci could be hidden in cells with brighter fluorescence. BL21(DE3) showed in some induced cells a stretched phenotype [Fig.2:B].

Sequence and Features