Difference between revisions of "Part:BBa K2728001"

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	===== Fig 4: Fluorescent strength vs Formaldehyde concentration =====		===== Fig 4: Fluorescent strength vs Formaldehyde concentration =====
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Revision as of 11:12, 14 October 2018

pfrmR - An Engineered Formaldehyde-Inducible Promoter

Basic Description

This promoter is an engineered formaldehyde-inducible promoter. Escherichia coli has a native formaldehyde-inducible promoter, pfrm, which is found upstream of the frmRAB formaldehyde detoxification operon. FrmR, the first product of the operon, is a member of the DUF156 family of DNA-binding transcriptional regulators. It binds the frmRAB promoter region and is negatively allosterically modulated by formaldehyde. FrmR is specific to formaldehyde, responding to acetaldehyde, methylglyoxal, and glyoxal to far lesser degrees and not at all to a range of other aldehydes and alcohols tested. The genes frmA and frmB encode a formaldehyde dehydrogenase and S-formylglutathione hydrolase, respectively, and are responsible for detoxifying formaldehyde to formic acid in a glutathione-dependent pathway. The negative-feedback regulation of the frmRAB operon is similar to that of many other prokaryotic operons, whereby the transcription factor represses its own transcription.

Fig 1: Without Formaldehyde

Fig 2: With Formaldehyde

Features

1. It’s a formaldehyde-inducible promoter from E.coli.
2. It’s an engineered promoter. It retains formaldehyde responsiveness, with 2-fold higher GFP expression in response to 100 μM formaldehyde than the native pfrm. Application of this promoter with higher basal and induced expression levels before methanol assimilation genes achieves higher biomass titers than the native E. coli pfrm.

Origins

Escherichia coli

Improvements and Experimental Characterization

The sequence of this part was taken from the research of Rohlhill J. etc. The 2 binding sites of variations are -35 and -10 (Fig ). We ordered synthesized plasmid with pFrmR and EGFP from Gensceipt and constructed pFrmR-EGFP-FrmR reporter system on plasmid pUC57. After dosing formaldehyde of 100 to 400uM, we tested the EGFP expression to identify the activity of the formaldehyde induced response of this prompter.
The research conducted by Rohlhill J. etc. has proved that, pFrmR retains formaldehyde responsiveness, with 2-fold higher GFP expression in response to 100 μM formaldehyde than the native pfrm (BBa_K749008 )[4].
Compared with the research of Rohlhill J. etc. (Fig ), unfortunately we were not able to detect any fluorescence after several rounds of repeating experiments (Fig ). This result did not necessarily indicate that there was no activity of this promoter. One of the probable reason to cause this, might be that the concentration of formaldehyde that entered the cells was not strong enough, thus the expression level of FrmR and the level of formaldehyde was unbalanced. Most of the FrmR binded with pFrmR, therefore repressed the activity of pFrmR, which means, pFrmR was at a inhibited status.
Future Improvements: We plan to optimize our reporter vector by introducing an independent promoter pLac to regulate the expression of FrmR.

Fig 1: Sites of mutants

Fig 2: Comparison of activity

Fig 3: Current reporter system

Fig 4: Fluorescent strength vs Formaldehyde concentration

Fig 5: Future reporter system

Parts Verification Before Submission

We verified our parts in the lab before submission. They are reliable! Please feel free to apply them onto your project.=)

Fig 1: PCR (to get targeted genes)

Fig 2: Restriction Digestion

Fig 3: Ligation

Fig 4: Colony PCR

Fig 5: Gel Verification

Sequence and Features