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Module 2: Auxin Xpress

Auxin, or Indole 3-acetic acid (IAA), is a plant growth hormone which is produced by several soil bacteria. We have taken the genes encoding the IAA-producing pathway from Pseudomonas savastanoi and expressed them in Escherichia coli. Following chemotaxis towards the roots and uptake by the Phyto Route module, IAA expression will promote root growth with the aim of improving soil stability.

Overview

Auxin is a well known plant hormone that is responsible for plant growth in response to biotic and abiotic stresses. Usually, synthetic auxins like α-Naphthaleneacetic acid (αNAA) and 2,4-Dichlorophenoxyacetic acid (2,4-D) are used as herbicides. They have been been used effectively for the past fifty years due to their high effectiveness and cheap cost. This high efficiency stems from the interactions that these auxin analogues have with the TIR1 protein. When the analogues bind to the TIR1 protein promoting the formation of the Aux/IAA–SCFTIR1. This leads to the ubiquitylation of of Aux/IAA which usually acts as an inhibitor when bound to ARF transcription factors. Many of the plant's genes are under the control of the ARF transcription factor meaning that any alteration can have a large impact on the plant's morphology. When altered by persistent compounds that cannot be degraded easily (such as synthetic auxins), the plant suffers as it is not able to keep up with the high metabolic demand correlated with over-expression of genes.

Therefore, we believe that natural auxin will not function as a herbicide because it is a labile chemically that can be easily metabolized by the plants. However, there is still a danger that too much natural auxin can also be detrimental to the plants. Therefore, for this module we must consider this fact during our design process. The bacteria must be able to produce a certain amount of auxin and must not go above a certain threshold. This level of control makes it a perfect project for synthetic biology which is looking to design controllable components in natural systems.

Our specifications will therefore be influenced by our modelling as well as our experiments on Arabidopsis thaliana. These experiments include an auxin concentration assay where we will be looking at the effect of auxin on the root length as well as the total dry mass of the plant in phytogel and soil. We will also be looking through past literature in order to determine what concentrations of auxin are known to promote root growth. However, seeing as how we only have ten weeks for the project and these sorts of studies take a long time, we must create a construct that will be able to produce auxin and will be as modular as possible to allow for easy tinkering in later stages. We have decided to use the IAM pathway from Pseudomonas savastanoi since it has been shown to be expressed in Escherichia coli and is only composed of two enzymes.

For the first design of our Auxin Xpress module we decided to make it as modular as possible. We have introduced an insulator sequence which will allow us to test out different promoters in the future until we find a combination of components that will fit our specifications. We also decided to use a variant of the Pveg promoter to contribute further to our modularity as well as codon optimizing our sequences for both Bacillus subtilis and Escherichia coli. Th