Improvement of an Existing Part
Describe the improvements your team made of an existing part.
Describe the improvements your team made of an existing part.
In order to increase the expression of protein of interest, we added a canonical strong RBS (Part:BBa_B0034) with a leader sequence containing a stem loop from the T7 bacteriophage gene 10 (g10.RBS, Part:BBa_K4150000).
The g10 leader sequence encodes very highly expressed phage proteins, in which 9-base of Epsilon motif exhibits perfect complementary to the 16S RNA of E. coli1. This structure connected with the consensus Shine-Dalgarno sequence (SD) can enhance up to 340-fold heterologous gene expression in E. coli2. The g10 leader sequence is also present in several commercially available pET series vectors.
We replaced the RBS with g10.RBS in BioBrick Part:BBa_K3431048 (T7- RBS-RFP-Tr) to create an improved BioBrick Part:BBa_K4150002 (T7-g10.RBS- RFP-Tr). These two plasmids were transformed into E. coli BL21. In the presence of IPTG, colonies on the LB agar plate and cultures in the LB broth both showed darker red colors for RFP gene expression driven by T7 promoter with g10 leader sequence compared to the original RBS without g10 leader sequence (Fig. 1). However, the E. coli BL21 with T7-g10.RBS-RFP-Tr had a higher background level in the absence of IPTG.
Figure 1 | The plasmids as indicated were transformed into E. coli BL21. The E. coli were grown on LB agar plate supplemented with 20 μg/mL of chloramphenicol and 1mM of IPTG. One of the colonies was cultured in LB broth with 34 μg/mL of chloramphenicol in the absence or in the presence of 1mM of IPTG. Inset panel: The plates were observed under a blue LED light box.
Furthermore, the transformed E. coli with T7-g10.RBS-RFP-Tr compared to T7-RBS-RFP-Tr expressed RFP at faster and increased (up to 2.5-fold) fluorescence intensity levels in a time-dependent manner (Fig. 2). The above data demonstrated the g10 leader sequence in front of RBS can significantly enhance gene expression.
Figure 2 | The plasmids as indicated were transformed into E. coli BL21. The E. coli were grown in LB broth supplemented with 34 μg/mL of chloramphenicol and 1mM of IPTG for 18 hr. The RFP expression levels were read at ex/em = 584/607 nm in a kinetic mode by Synergy H1 Hybrid Multi-Mode Reader - BioTek Instruments (Agilent Technologies, Inc.). The values of fluorescence intensity were presented by the data with IPTG induction minus the data without induction as background levels.
According to our structure study and functional analysis of T7 gene 10 leader sequence in the transformed E. coli, we clarified an enhanced RBS, named g10.RBS. The g10.RBS in the context of T7 promoter and T7 terminator can increase the RFP gene expression displayed as red color on colonies and liquid culture, as well as measured in a fluorescence kinetic mode (584 nm excitation and 607 nm emission) by a microplate reader. This improved BioBrick part of Part: BBa_K4150002 can benefit both in vitro and in vivo gene expression for future iGEM projects.