In our story, E. ninja retires from being an undercover warrior, and turns to farming (Fig. 0.1). Our improved part for phosphate sensing and a new part for cytokinin synthesis will lead us to our goal to create “Farmer E.coli ” that could increase plant growth by synthesizing several plant hormones depending on the soil environment. As for sensing soil nutrients, we focused on phosphate and nitrate because these are said to be especially important for plants. When nutrient levels are low, plants are in danger of withering. Therefore, we are proposing E. coli to produce the plant hormone “auxin,” which promotes the growth of plants’ roots (Fig. 0.2). Also, when the soil is rich in nutrients, plants can grow quickly. Therefore, we want to make E. coli produce the plant hormone “cytokinin,” which promotes the growth of plants’ shoots.

Our “Farmer E. coli “ can be implemented by combining our improved phosphate sensor part (BBa_ K1139210), our newly constructed cytokinin production part and two pre-existing parts which are the nitrate sensor part (Edinburgh 2009, BBa_K216005) and the auxin production part (Imperial College 2011, BBa_K515102) (Fig. 0.2). Because the phosphate sensor part by OUC-China 2012 (BBa_K116401) had insufficient data, we improved the part by using a different promoter. We also learned methods for quantitative analysis for cytokinin through bioassay of cucumber seed sprouts (Fig. 3) and through using ultra-performance liquid chromatography (UPLC).

In addition, to achieve the natural plants’ temporal pattern for producing plant hormones in E. coli, we introduced “Incoherent feed forward loop,” including new hybrid promoter part (BBa_K1139150). Our mathematical model for this system predicted that we can create temporal pattern for plant hormone production.

We have improved a phosphate sensor part which includes the inducible promoter of the alkaline phosphatase gene (phoA) from E.coli (M. Dollard et al., 2003). This promoter is repressed by high phosphate concentrations (Fig.1.1). To know more about the mechanism of this promoter, please click here.（PphoAアッセイページのintroductionへリンク） We amplified the phoA promoter from E. coli. (MG1655) and ligated this promoter into GFP part to construct the new part (BBa_K1139210parts registryリンク)for assay. We then introduced this new part into E.coli (MG1655). Fig. 1.2 shows the result of an induction assay. It shows that the increase in phosphate concentration repressed the phoA promoter. Especially, we see that the phoA promoter is drastically repressed at phosphate concentrations of 100 to 300μM. Compared to OUC-China’s phosphate sensor part including phoB promoter (Fig. 1.3), our phosphate sensor part shows clearer result. Our phosphate sensor part has been submitted (BBa_K1139210 improved part) (Fig. 1.1). To know more about this assay, please see here.（PphoAアッセイページへリンク）

In order to construct cytokinin production part, we focused on AtIPT, a plant enzyme which catalyzes the synthesis of cytokinin. The mechanisms of cytokinin synthesis are shown in Fig. 2.1 (Takei et al., 2001). We ordered two DNA sequences of AtIPT (AtIPT4 and AtIPT7) derived from A. thaliana and are now constructing the part including one of them.

AtIPT, a plant enzyme, catalyzes the synthesis of iPRMP from DMAPP and AMP. According to the previous research, DMAPP, and AMP are provided by authentic metabolism in E. coli . It is also expected in the report that E. coli also has the enzymes which catalyze the synthesis of iP or tZ from iPRMP.

Before constructing genetic parts for cytokinin synthesis, we learned methods for quantitative analysis for cytokinin through bioassay of cucumber seed sprouts (Flethcer et al., 1971, Porra et al., 1989) and through using ultra-performance liquid chromatography (UPLC).

In our bioassay of cucumber seed sprouts, we saw how cytokinin acts on plants. We planted the seeds and germinated for 5 days. Then, we cultivated the sprouts in standard cytokinin sample solutions. After 24 hours, we measured the weight of the sprouts and also homogenized them to measure the concentration of chlorophyll (Fig. 3.2C). Fig. 3.1 shows the result that cytokinin increased the weight of the sprouts and the concentration of chlorophyll. The quantitative results are also shown in Fig. 3.2A, B (iP, tZ are both sorts of cytokinin). To know more about this assay, please see here.（バイオアッセイページへリンク）

(A) The weight of the seed sprouts iP : 6-(γ, γ-Dimethylallylamino) purine, tZ : trans-zeatin (B) The concentration of chlorophyll (right) The absorbance of the supernatant was read at 663.6 and 646.6 nm. Calculation of concentration of the chlorophyll was carried out as described by Porra et al.,1989 (3) (C) The extracted chlorophyll

Through ultra-performance liquid chromatography (UPLC), we plan to confirm that our “Farmer E. coli” actually produce cytokinin. Before completing the system to make E. coli produce cytokinin, we determined the retention times of iP and tZ in UPLC by using authentic samples of iP and tZ. The results are shown in Fig. 3.4. To see the detail method of this experiment, please click here.（UPLCのページへリンク）

In order to achieve the natural plants’ temporal pattern for producing plant hormones in E. coli, we introduced an incoherent feed forward loop including new hybrid promoter part (BBa_K1139150). Plants produce their hormones transiently rather than steadily (Takei et al., 2001). Moreover, continuous overexpression of hormones can be harmful to plants (K. Thiman, 1937). Thus, we thought that it should be important to achieve this transient temporal pattern for producing plant hormones in E.coli. The system of our designed incoherent feed forward loop (Mangan S et al., 2006) is shown in Fig. 4.1. We newly developed PRM/lac hybrid promoter, which is activated by CI and repressed by LacI (Fig. 4.2). We plan to ligate a hormone synthase part downstream of this hybrid promoter. Our mathematical model (Fig. 4.3) shows what the temporal pattern for plant hormone production should achieve. While PRM/lac activation by CI is a single step, repression by LacI is a two-step reaction. Thus, the activation of PRM/lac is faster than its repression. This time lag between activation and repression is important for generating a temporal pattern of plant hormone production.

As a first step to achieve this incoherent feed forward loop, we constructed the circuit shown in Fig. 4.5 to confirm that our new PRM/lac hybrid promoter actually works. We set GFP as the output of PRM/lac hybrid promoter and introduced the circuit into E.coli . We have already confirmed that our new PRM/lac hybrid promoter is actually activated by CI through an induction assay (Fig. 4.7). This part has been submitted (BBa_K1139150 new part). Details about this assay can be found here.（PRM/lacアッセイページへリンク） We are now assaying induction in response to combinations between CI and LacI.

Our project will be applied to studying the plants’ response to external plant hormones. We programmed an incoherent feed forward loop to our new device of plant hormone production. By applying the incoherent feed forward loop, we can achieve pulse-generation of the output (Basu. S et al., 2003). Moreover, the pulse wave can be customized with changing the parameters, for example, intensity of promoters and various interactions. Utilizing the incoherent feed forward loop, we aim to construct artificial pulse-generator circuits which can output plant hormones in various pulse waves. Various artificial genetic circuits which can change the output chronologically, including incoherent feed forward loop, have been reported (Elowitz et al., 2000, Eileen et al., 2005). By combining plant hormone synthesis genes to these artificial genetic circuits, we will be able to make E. coli produce plant hormones in chronological patterns. Analyzing the response of plants to plant hormones given in temporal change leads to elucidate not only the sensitivity of plants’ response to plant hormones but also the abilities of plants in signal transduction. Therefore, our project contributes to constructing the pulse-generator for plant hormones using E.coli . Findings in plant science using this strategy must be important for contributing to agriculture and furthermore solving worldwide food shortages. We hope to meet public expectations by realizing agriculture aid by bacteria, though there may be some difficulties.