Difference between revisions of "Part:BBa K2997008"

Revision as of 14:54, 19 October 2019

Native promoter-pchR-sfGFP

Background

As part of our project, we decided to make a device that can sense p-Cresol. According to our research [1], we have discovered a group of bacteria known as Pseudomonas which can sense p-Cresol naturally. In a previous study, the ability of Pseudomonas to sense p-Cresol is used by them to detect p-Cresol in the environment.

Part Construction & Experimental Results

The pchR-GFP (BBa_K2997008) was constructed from IDT DNA synthesis in the form of 3 gBlock gene fragments via overhang PCR. Then, we performed digestion on the finished part and ligated it into the pSB1C3 vector. Subsequently, we transformed the pchR-GFP construct (BBa_K2997008) into E. coli Top 10 using electroporation. After allowing the transformed E. coli Top 10 to grow on LB with Cm (Chloramphenicol) plates, colony PCR and sequencing was carried out to determine successful clones. The colony PCR results indicated that the E. coli has pSB1C3 with pchR-GFP. However, after several attempts to construct pchR-GFP, all the sequencing results indicated mutations occurred on all of our samples.

These results led us to hypothesize that the pchR protein is toxic to our E. coli. Moreover, according to a research paper [9] we have found, it is suggested in the study that p-Cresol is toxic to Gram-negative bacteria, which includes E. coli. Hence, this plasmid construct has been dropped.

Therefore, the construction of pchR-GFP was carried out again by re-doing overlap PCR, where we combine all the three IDT gene fragments into the full length pchR-GFP construct. For this time, the finished full length pchR-GFP part was then inserted into the vector pBBR1 MCS-4 (carries ampicillin resistance gene).

However, due to the complications surrounding the selection marker being used (Ampicillin), we were not able to get a definitive result that indicates that we have positive colonies. This is due to the fact that P.fluorescens 55 and P.aeruginosa PAD1 are naturally resistant to ampicillin and the vector we used for our construct carries ampicillin resistance gene. Hence, positive colonies cannot be differentiated with negative colonies. Besides that, our colony PCR results on the single colonies were also proven to be negative.

Therefore, with time being one of the factors, we decided to drop any further construction and functional experiments surrounding the p-Cresol sensing part (pchR-GFP).

Mechanism and Biology

The construct is primarily centered upon Pseudomonas fluorescens (PC24) [2][3], as it has a gene cluster that consists of a positive inducible operon, pchR, which allows it to sense p-Cresol and promote the transcription of the downstream region to degrade the p-Cresol. The pchR gene can be translated into activator proteins that can bind with the inducer (p-Cresol) and leads to the conformation of the protein. As a result, the activator protein binds with p-Cresol and the eventual protein-p-Cresol complex will then bind onto the p-Cresol sensing region that is placed just downstream of pchR and start transcription of the gene downstream.

Sequence and Features

References

1. Cho, Ah Ra, Eun Jin Lim, Yaligara Veeranagouda, and Kyoung Lee* Department of Microbiology, Changwon National University, Changwon-si, Kyongnam 641-773, Korea . Identification of a p-Cresol Degradation Pathway by a GFP-Based Transposon in Pseudomonas and Its Dominant Expression in Colonies
2. Merike Jo ˜esaar, Eeva Heinaru, Signe Viggor, Eve Vedler & Ain Heinaru Institute of Molecular and Cell Biology, Tartu University, Tartu, Estonia. Diversity of the transcriptional regulation of the pch gene cluster in two indigenous p-Cresol-degradative strains of Pseudomonas fluorescens
3. Jae Jun Jeong,13 Ji Hyun Kim,1 Chi-Kyung Kim,2 Ingyu Hwang3 and Kyoung Lee1 3- and 4-alkylphenol degradation pathway in Pseudomonas sp. strain KL28: genetic organization of the lap gene cluster and substrate specificities of phenol hydroxylase and catechol 2,3-dioxygenase