Team:ECUST/Parts



New Parts

# Name Type Description Designer Other
1 BBa_K2308001 composite part knock out (upstream1+downstream1) Yunpeng Dai
2 BBa_K2308002 composite part knock in (upstream2+sYFP2+downstream2) Yunpeng Dai
3 BBa_K2308003 basic part sYFP2 Yunpeng Dai improvement of BBa_K864100
4 BBa_K2308004 composite part knock out (upstream1+promotor+Amp+downstream1) Yunpeng Dai
5 BBa_K2308005 composite part knock in (upstream2+sYFP2+promotor+Amp+downstream2) Yunpeng Dai
6 BBa_K2308006 basic part upstream1 Yunpeng Dai
7 BBa_K2308007 basic part downstream1 Yunpeng Dai
8 BBa_K2308008 basic part upstream2 Yunpeng Dai
9 BBa_K2308009 basic part downstream2 Yunpeng Dai
10 BBa_K2308010 basic part Amp promotor Yunpeng Dai
11 BBa_K2308011 basic part Amp coding Yunpeng Dai
12 BBa_K2308012 basic part LacIq repressor Yunpeng Dai
13 BBa_K2308013 basic part LacIq spacer Yunpeng Dai
14 BBa_K2308014 basic part LacIq promotor Yunpeng Dai
15 BBa_K2308015 basic part LacIq coding Yunpeng Dai
16 BBa_K2308016 composite part LacIq regulator Yunpeng Dai improvement of BBa_v1003

Improvements

The reporter sYPF2 has been codon-optimized for Rhodobacter sphaeroides 2.4.1 and it was successfully tested as a reporter in this chassis. We have made several measurements to show its fluorescence in Rhodobacter sphaeroides 2.4.1 as well its properties (Fluorescence excitation/emission spectrum).

To learn more about the improvement ,please click here.

The regulator LacIq's coding sequences are submitted in part BBa_K2308016. In our project, we used this part with Part:BBa_K2308003 together to turn Rhodobacter sphaeroides 2.4.1 into inducible strains and successfully induced the expression of sYFP2.

To learn more about the improvement ,please click here.


Key parts

BBa_K2308002 is an important part in our experiment. It is composed of BBa_K2308006,BBa_K2308003 and BBa_K2308007. The function of this part is to carry out the homologous recombination on the genome of Rhodobacter sphaeroides 2.4.1.



To learn more about this part ,please click here.



sYFP2(BBa_K2308003) is the key part in our experiment. It is used both for fusion expression (see BBa_K2308002) and inducible cytoplasm expression (combined with BBa_K2308016), and the host cell is Rhodobacter sphaeroides 2.4.1.


In inducible cytoplasm expression experiment, we used part BBa_K2308016 to turn the Rhodobacter sphaedoides 2.4.1 into inducible strains, and IPTG was added (800 μM in final volume)when the OD700 of the strain was about 0.4(grown for about 24h).



To learn more about this part , please click here.



This part contains LacIq repressor, LacIq spacer, LacIq promotor and LacIq coding sequence and is used for Rhodobacter sphaeroides 2.4.1, cells with the device can carry out inducible expression of the target proteins.


In inducible cytoplasm expression experiment, we used part BBa_K2308016 to turn the Rhodobacter sphaeroides 2.4.1 into inducible strains, and IPTG was added (800 μM in final volume)when the OD700 of the strain was about 0.4(grown for about 24h).



To learn more about this part ,please click here.