Phenazine

Overview

Figure 1: Principle of electron transfer from bacteria to anode via mediators as electron shuttle.

Of great interest is the production of endogenous mediators. The overexpression of glyceroldehydrogenase in E. coli is a promising approach. Because many derivates of glyceroldehydrogenase are small, water-soluble redoxmolecules, they have the properties of a mediator. Futhermore, it will be tested, if there is a possibility of expressing the mediator phenazin. Phenazin is an endogenous mediator of Pseudomonas species.

Theory

Phenazines comprise a large group of heterocyclic nitrogen-containing substances, having a tricyclic ring in its core. They are substituted at different points around their rings, which alters water solubility and other properties. After discovery of naturally occurring phenazines, more than 6000 were chemically synthesized. (Mavrodi, [http://www.ncbi.nlm.nih.gov/pubmed/16719720 2006]). [http://en.wikipedia.org/wiki/Neutral_red Neutral red], a well-known pH-indicator, also belongs to this class.

Phenazine derivatives were one of the first secondary bacterial metabolites that were consequently studied since their discovery in 1859. The first substance of this family, a blue pigment of Pseudomonas aeroguinosa, was called [http://en.wikipedia.org/wiki/Pyocyanine «pyocyanine»]. It had antimicrobial properties that raised further interest in these substances. Phenazines are produced by many bacterial specie, but they are mostly studied in representatives of fluorescent pseudomonads. A single bacterial strain usually produces two or more species-specific phenazines, except Pseudomonas fluorescens, that is known to produce only PCA ([http://www.ebi.ac.uk/chebi/chebiOntology.do?chebiId=CHEBI:62412 phenazine-1-carboxylic acid]). (Mavrodi et al., [http://www.ncbi.nlm.nih.gov/pubmed/11591691 2001])

Biologically phenazines are known for their broad-spectrum antibiotical, antiparazitar and even anti-malaria properties (Handelsmann et al., [http://www.plantcell.org/content/8/10/1855.long 1996]). They are highly associated with pathogenicity of bacterial species. A broad-range, non-specific mechanism of phenazine action was firstly thought to be aimed against an essential metabolic pathway (Leo C. Vining, [http://www.annualreviews.org/doi/pdf/10.1146/annurev.mi.44.100190.002143 1990]), but potentiometric measurements on PYO discovered a redox system, that was formed between its reduced and oxidised derivatives. Consequently it was shown, that almost all properties of phenazines could be attributed to their ability to undergo redox transformations (Muller, [http://www.ncbi.nlm.nih.gov/pubmed/8541351 1995]). This acknowledgement brought an idea, that these molecules can be used as an electron shuttle in a MFC. Indeed, it was shown that external addition of phenazines, both PCA and PCN ([http://www.ebi.ac.uk/chebi/searchId.do?chebiId=62240 phenazine-1-carboxamide]) alike, causes a significant raise of current flow (The Hai Pham, [http://www.ncbi.nlm.nih.gov/pubmed/18688612 2008]). Surprising, a mixed culture of phenazine-secreting and phenazine non-secreting strains showed similar results, proving that phenazine can be used for redox cycling not only by its producer (Hernandez et al. [http://www.ncbi.nlm.nih.gov/pubmed/14766572 2004]). A group of soilborne, root-desease controlling microorganisms, such as Pseudomonas fluorescens and Pseudomonas chlororaphis, are known to produce phenazine compounds PCA and PCN. They belong to safety class S1, so we saw our chance to try a heterologous expression, taking the coding sequences from one of the known phenazine producers. There were already reports of successful phenazine expression in E.Coli (MacDonald et al. [http://www.ncbi.nlm.nih.gov/pubmed/11562236 2001])

The phenazine synthesis is a branch-off of a [http://en.wikipedia.org/wiki/Shikimic_acid| shikimic acid] pathway that delivers aromatic acids. It was discovered and researched in detail for Pseudomonas aeroguinosa and Pseudomonas fluorescens 2-79. A seven-gene cluster was [http://www.ncbi.nlm.nih.gov/nuccore/L48616.1 phzABCDEFG] was identified, that was to almost 95% identical in both organisms.

Figure 2: Comparison of sequences between enzymes in phenazine cluster and other proteins with known function, according to research of [http://www.ncbi.nlm.nih.gov/pubmed/11562236 MacDonald et al. 2001.]

Also research on phenazine diversity and genetic evolution, (Mavrodi, [http://www.ncbi.nlm.nih.gov/pubmed/20008172 2010]) brought us to a thought, that many species of fluorescent pseudomonas have the corresponding sequences and are able to produce phenazines. We have already thought over a cloning strategy, but the fact, that phenazines are highly associated with pathogenicity of bacterial species, was a serious concern about biological safety of constructing a strain, overexpressing phenazines. We were uncertain, if this is an appropriate option and what consequences can we await.

Genetic Approach

Figure 2: Phenazine synthesis cluster, comprising an autoinducer synthase (phzI) gene, positive regulator protein (phzR) and coding [http://www.ncbi.nlm.nih.gov/nuccore/L48616.1 phzABCDEFG genes.]

A close look on the cluster revealed seven forbidden restriction sights, making a cloning in accordance with the iGEM-rules an ultimate challenge for a short-termed project. At first, we still pursued the idea and tried to multiply the phenazine-producing cluster, a 8505 bp long fragment by PCR. Unfortunately, this step did never success. We varied different parameters and tried different enzymes, but we have always seen a false priming and multiple amplificates. Considering all these arguments, we realized that this sub-project will be impossible to pursue in the time we had, and even if we succeed, a strain, producing a natural antibioticum acting as a mediator was very questionable from the biosafety point of view. So we decided to look for applicable alternatives. Riboflavin, a natural mediator that is not associated with any pathogenicity seemed an alternative of choice and our decision was rewarded by successful results.

Results

References

• Mavrodi D.V, Tomashow L.S. (2006) Phenazine compounds in fluorescent Pseudomonas spp. biosynthesis and regulation. [http://www.ncbi.nlm.nih.gov/pubmed/16719720 Annual review of Phytopathology 44:417– 445]
• Mavrodi DV, Bonsall RF, Delaney SM, Soule MJ, Phillips G, Thomashow LS (2001) Functional analysis of genes for biosynthesis of pyocyanin and phenazine-1-carboxamide from Pseudomonas aeruginosa PAO1. [http://www.ncbi.nlm.nih.gov/pubmed/11591691 J Bacteriol 183:6454–6465]

• Handelsman, J. and E. V. Stabb (1996) Biocontrol of soilborne plant pathogens. [http://www.plantcell.org/content/8/10/1855.long Plant Cell 8(10): 1855-69.]

• Vining L.C. (1990). Functions of secondary metabolites. [http://www.annualreviews.org/doi/pdf/10.1146/annurev.mi.44.100190.002143 Annu Rev Microbiol: 44:395-427]

• Muller M. Scavenging of neutrophil-derived superoxide anion by 1-hydroxyphenazine, a phenazine derivative associated with chronic Pseudomonas aeruginosa infection: relevance to cystic fibrosis. (1995) [http://www.ncbi.nlm.nih.gov/pubmed/8541351 Biochim Biophys Acta: 1272(3):185-9.]

• Pham T.H. (1998) Use of Pseudomonas species producing phenazine-based metabolites in the anodes of microbial fuel cells to improve electricity generation. [http://www.ncbi.nlm.nih.gov/pubmed/18688612 Appl Microbiol Biotechnology: 80(6):985-93.]

• Hernandes M.E (2004) Phenazines and other redox-active antibiotics promote microbial mineral reduction [http://www.ncbi.nlm.nih.gov/pubmed/14766572 Appl Environ Microbiol.:70(2):921-8.]

• McDonald M, Mavrodi DV, Thomashow LS, Floss HG. (2001). Phenazine biosynthesis in Pseudomonas fluorescens: branchpoint from the primary shikimate biosynthetic pathway and role of phenazine-1,6-dicarboxylic acid. [http://www.ncbi.nlm.nih.gov/pubmed/11562236 J. Am. Chem. Soc. 123:9459–60]

• Mavrodi D.V. (2010) Diversity and evolution of the phenazine biosynthesis pathway. [http://www.ncbi.nlm.nih.gov/pubmed/20008172 Appl Environ Microbiol.:866-79.]