"
Team:BNU-China/investigatin.html
From 2014.igem.org
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Overview
The plants root exudates contain TCA intermediates that can attract bacteria having the ability of chemotaxis. Click here to learn more about root exudates. E.coli has five kinds of chemoreceptors, which interact with factors of the flagella that leads to chemotaxis. But E.coli doesn’t have specific chemotaxis towards some TCA intermediates while Pseudomonas putida has some McpS, like McfQ and McfR. We made a part BBa- containing the sequence of McfR, which detects succinate, malate and fumarate. Then we detected its chemotaxis towards malate and succinate, you can download our protocol which is based on the work 2011_Imperial_College_London had done before.click here to see the results. At last, we designed a model to mimic the movement pattern and predict the efficiency of the Prometheus E.coli.
Root exudates
Plants secrete both high- and low-molecular weight compounds from their roots, and these root exudates play an important role not only as nutrients for soil microbes but also as signal molecules in plant–microbe interactions (Sugiyama & Yazaki). In the wild, legume plants establish symbiotic interactions with rhizobia and arbuscular mycorrhizal fungi to obtain several nutrients such as nitrogen and phosphate. The root exudates of legume plants contain organic acids, including some TCA intermediates, such as malate, succinate, citrate and fumarate. Especially, in response to phosphorus starvation, malonie, succinic, fumaric, malic, citric, and t-aconitic acids were detected in the root exudates(Ohwaki & Hirata, 1992). Here, we design the Prometheus E.coli that responses to malate and succinate and will swim to the roots to improve the interaction between the roots and fungi.
Chemoreceptor and Chemotaxis
In isotropic chemical environments, E. coli swims in a random - walking pattern produced by alternating episodes of counter-clockwise (CCW) and clockwise (CW) flagellar rotation (Fig. 1, left panel). While an attractant or repellent appear somewhere in the environment, the cells’ locomotor responses specific runs that take the cells in favorable directions (toward attractants and away from repellents), resulting in net movement towards preferred environments. (Fig. 1, right panel).
Fig. 1 Random and biased walks. Left: A random walk in isotropic environments. When the cell's motors rotate CCW, the flagellar filaments push the cell forward. When one or more of the flagellar motors reverses to CW rotation, that filament undergoes a shape change (owing to the torque reversal) that disrupts the bundle. Until all motors once again turn in the CCW direction, the filaments act independently to push and pull the cell in a chaotic tumbling motion. Tumbling episodes enable the cell to try new, randomly-determined swimming directions. Right: A biased walk in a chemoeffector gradient. As cells swim up a concentration gradient of attractant, they spend more time smooth swimming than tumbling; this modulation of swimming behavior is manifested as a chemotactic response.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
E. coli has five chemoreceptors, four are methyl-accepting chemotaxis proteins (McpS) which have periplasmic ligand binding sites and conserved cytoplasmic signaling domains (Fig. 2). The McpS initiate a motor control response and a feedback circuit that updates the methylation record to achieve sensory adaptation and cessation of the motor response. A fifth MCP-like protein, Aer, mediates methylation-independent aeroTCAtic responses by monitoring redox changes in the electron transport chain. The five MCP-family receptors in E. coli utilize a common set of cytoplasmic signaling proteins to control flagellar rotation and sensory adaptation (Fig. 2). CheW and CheA generate receptor signals; CheY and CheZ modulate rotation of the flagellar motor and thus change cell behavior and movement; CheR and CheB regulate MCP methylation state to make feedback to CheW and CheA.
Fig. 2 Signaling components and circuit logic. E.coli receptors employ a common set of cytoplasmic signaling proteins: CheW and CheA interact with receptor molecules to form stable ternary complexes that generate stimulus signals; CheY transmits those signals to the flagellar motors, CheZ controls their lifetime; CheR (methyltransferase) and CheB (methylesterase) regulate MCP methylation state. Abbreviations: OM (outer membrane); PG (peptidoglycan layer of the cell wall); CM (cytoplasmic membrane).
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
But the original chemoreceptors of E.coli do not respond to the root exudates, while the McpS of the Pseudomonas putida , McfQ and McfR do(Parales, et al.). McfQ responds to citrate and fumarate, and McfR detects succinate, malate and fumarate. To compare with the work what 2011_Imperial_College_London had done, we chose McfR which also responds to malate. The mechanisms of prokaryote chemoreceptors are similar, so we designed a plasmid to express chemoreceptor. McfR in the E.coli makes the bacteria have the ability of chemotaxis towards TCA intermediates. As our experimental condition is limited, we just did experiments on chemotaxis towards succinate and malate. What’s more, in an attractant gradient, the chemoreceptors monitor chemoeffector concentration changes as they move around. And they use that information to modulate the probability of the next tumbling event. And we searched the pattern of their chemotaxis towards a concentration gradient of attractant using capillary assay. The results are demonstrated below.
Results
We did both agar assay and capillary assay to detect the response of E.coli to different attractants and different concentrations of each attractant. Because the agar assay (Fig.3) is difficult to replicate and collect the data from, we just show the results of capillary assay (Fig.4) . We made a negative control using washing buffer and five concentration gradients (100mM/10mM/1mM/0.01mM/0.0001mM) of attractants. These E.colis were divided into three groups based on the plasmid they have been transformed into. The plasmids are biobricks, BBa_K608003 and BBa_K515102 (they are from 5A and 8F wells in plate1), and the McfR plasmid was designed by us. BBa_K608003 (5A) only has a strong promoter and medium RBS, so it doesn’t have specific chemotaxis towards TCA intermediates. BBa_K515102 (8F) is a biobrick from 2011_Imperial_College_London, which responds to L(-)malic acid (HO2CCH2CH(OH)CO2H).
Fig.3 Agar assay: The three plates shows the chemotaxis results of 8F towards three kinds of attractants, malate, citrate and succinate from left to right. The filter paper of attractants is put on the left, the PBS is put on the right, bacteria is in the middle. Here, 8F swims fastest to malate.
Fig.4 E. coli’s ability of chemotaxis towards different concentrations of succinate or malate.
The cells were diluted 20000 times. 5A is a control which doesn’t have chemotaxis towards malate or succinate.
Malate: 8F showed the strongest respond. The tendency of curve of 8F was biphasic with maximums at attractant concentration of about 10-2 M and 10-5 M, and reached minimum at attractant concentration of about 10-1 M, which is similar to others’ work. With attractant concentration decreasing for 8F, the number of cells decreased slowly. McfR stayed stable at range of 10-7 M to 10-3 M, and had only one phase which reached its maximum at attractant concentration of 10-2 M, then it went down sharply at 10-1 M. There was a significant difference among 8F and 5A (p < 0.05), and quantity of cells of 8F was much more than that of 5A. So 8F has chemotaxis towards malate. On the other hand, McfR and 5A were not significantly different and quantity of cells of McfR was little less than it of 5A. So McfR shows no chemotaxis towards malate here.
Succinate: The tendencies of curves of 8F and McfR towards succinate are same. As the attractant concentration increased, the number of cells arose and reached the maximum at attractant concentration of about 10-2 M and fell sharply with the minimum at attractant concentration of 10-1 M. The quantities of cells of 8F and McfR were almost equivalent and did not have significant difference. But there were significant differences among 8F & 5A, and McfR & 5A: the number of cells of 5A are far less than 8F or McfR (p < 0.05), which demonstrated that 8F and McfR have chemotaxis towards succinate and the capacity of chemotaxis of 8F and McfR towards succinate are almost equal. Compared with chemotaxis towards malate, both of 8F and McfR show stronger chemotaxis towards succinate.
Analysis
The tendency of the chemotaxis towards chemical gradient may be influenced by two factors: pH and phosphorylation state of McpS. The motor of flagella is energized by a H＋ (or Na＋ in some species) gradient across the cytoplasmic membrane(Schmitt, 2003), but the mechanism is not clear. Lisa M. Maurer and Elizabeth Yohannes proved that low pH (at pH 5.0) induced the expression of some flagellar and chemotaxis genes and proton export, while coinducing oxidative stress and heat shock regulons to maintain internal pH homeostasis and to prepare the cell to survive future exposure to more extreme pH conditions (below pH 5 or above pH 9 which is higher or lower than the cytoplasmic pH 7.6)(Maurer, Yohannes, Bondurant, Radmacher, & Slonczewski, 2005). The pH of attractants showed below (Fig.5) is at the range of pH 1.0 – 6.4. The highest concentration of 0.1M is pH 1.0 of malate and 2.0 of succinate, which leads to weakest chemotaxis, for oxidative stress induces its protective responses more than chemotaixs genes expression; while the curves reach maximum at concentration of 0.01M because of the opposite reason.
Fig.5 The pH of the concentration gradients of malate and succinate. The pH of malate is lower than succinate at high concentration (10-1 and 10-2 M), and is equal with succinate at lower concentration. Both of them remain pH 6.4 at low concentration(10-5, 10-7 and 0 M).
On the other hand, the E. coli chemotaxis pathway is influenced by reversible McpS methylation and related proteins phosphorylation (Fig. 6). McpS, in response to chemoeffector stimuli, transfer the signals and make CheA autophosphorylated via the adapter protein CheW. Then phospho-CheA molecules serve as donors that transfer phosphoryl groups to specific aspartate residues in CheY and CheB. Phospho-CheY enhances CW rotation of the flagellar motors; phospho-CheB has high MCP methylesterase activity that helps to change the CW rotation to CCW rotation, and they will be inactive because of loss of phosphoryl group through spontaneous self-hydrolysis. CheZ further enhances the dephosphorylation rate of phospho-CheY to ensure rapid locomotor responses to changes in the supply of signaling phosphoryl groups to CheY. The signaling activities of chemoreceptors have two-state corresponding to two movement patterns separately (Fig. 6). Receptor complexes in the CW signaling state activate CheA, producing high levels of phospho-CheY. Receptors in the CCW signaling state deactivate CheA, resulting in low levels of phospho-CheY. Thus, the behavior of the flagellar motors reflects the relative proportion of receptor signaling complexes in the kinase-on and kinase-off conformations. For example, attractant ligands drive receptors toward the kinase-off state; subsequent addition of methyl groups shift receptors toward the kinase-on state, reestablishing the steady-state (adapted) balance between the two states and restoring random walk movements.
Fig. 6 Chemotaxis pathway. Reactions and components that augment CW rotation are depicted in green; those that augment CCW rotation are depicted in red.
Left: The flagellar motors of E. coli spin CCW by default of Che-Y; the signaling pathway modulates the level of phospho-CheY, the signal for CW rotation.
Right: The cartoons depict receptor ternary complexes in kinase-active (on) and kinase-inactive (off) signaling states. Changes in chemoeffector occupancy drive the complexes toward one state or the other. During sensory adaptation, changes in receptor methylation level shift signaling complexes toward the opposing state to restore a balance between CCW and CW signal outputs. The actual stoichiometry and structure of receptor signaling complexes are not known. Note that receptor methyl groups are attached to specific glutamic acid (E) residues in the MCP cytoplasmic domain, forming glutamyl methyl esters and neutralizing the negative charge on the glutamyl carboxyl group. Charge neutralization probably plays an important role in controlling receptor output state.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
Compared with the work of 2011_Imperial_College_London had done, we find that both of their biobrick BBa_K515102 and our biobrick BBa_K1405004 (originally found in P. aeruginosa and P. putida separately) have chemotaxis towards two kinds of TCA intermediates, malate and succinate (Fig.7 A). Estela Pineda-Molina, et al. reported high-resolution structures of the ligand- binding region of the cluster II McpS chemotaxis receptor (McpS-LBR) of Pseudomonas putida KT2440 in complex with malate and succinate (Fig.7 B& C) . The root mean square deviation (rmsd) between the malate and succinate cocrystal structure is only 0.2 Å indicating that differences in the nature of the ligand do not significantly alter the protein structure (Table 1). In a sequence alignment of McpS-LBR homologs containing McpS-LBR of Pseudomonas aeruginosa, the amino acids involved in malate and succinate binding are conserved. R60 is almost fully conserved, whereas the remaining residues are conserved to between 30–80% (Estela Pineda-Molina, et al.)
Table 1. Properties of the model
Fig.7 (A) The structure of malate and succinate, and the thermodynamic parameters for the 2 compounds that were found to bind. (B and C) View of the interaction of malate (B) and succinate (C) with the McpS-LBR. Malate binds to a cavity formed by α1 and the C-terminal segment of α6, and its coordination is achieved through interactions with R60, R63, R254, and T258 from one monomer and Q65 from the other monomer. Residues R60, R63, and Q65 form part of helix α1, whereas R254 and T258 are part of α6. Succinate binds to McpS-LBR in an almost identical manner as malate. Unlike malate, succinate has no hydroxyl group at C2. Therefore, the two hydrogen bonds that are established between the malate hydroxyl group, and the protein cannot be formed in the succinate structure. The remaining interactions of succinate with R60, R63, R254, and Q65 are analogous to the malate structure where they establish six hydrogen bonds.
Reference
Maurer, L. M., Yohannes, E., Bondurant, S. S., Radmacher, M., & Slonczewski, J. L. (2005). pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12. Journal of Bacteriology, 187(1), 304-319.
Ohwaki, Yoshinari, & Hirata, Hiroshi (1992). Differences in carboxylic acid exudation among P-starved leguminous crops in relation to carboxylic acid contents in plant tissues and phospholipid level in roots. Soil Science and Plant Nutrition, 38(2), 235-243.
Parales, Rebecca E, Luu, Rita A, Chen, Grischa Y, Liu, Xianxian, Wu, Victoria, Lin, Pamela, et al. Pseudomonas putida F1 has multiple chemoreceptors with overlapping specificity for organic acids. Microbiology, 159(Pt 6), 1086-1096.
Schmitt, R. (2003). Helix rotation model of the flagellar rotary motor. Biophysical Journal, 85(2), 843-852.
Sugiyama, Akifumi, & Yazaki, Kazufumi. Root exudates of legume plants and their involvement in interactions with soil microbes Secretions and exudates in biological systems (pp. 27-48): Springer.
Pineda-Molina, E., Reyes-Darias, J. A., Lacal, J., Ramos, J. L., García-Ruiz, J. M., Gavira, J. A., & Krell, T. (2012). Evidence for chemoreceptors with bimodular ligand-binding regions harboring two signal-binding sites. Proceedings of the National Academy of Sciences, 109(46), 18926-18931.
*You can download the protocol of this part here: Protocol on Delivery System.pdf
Overview
The plants root exudates contain TCA intermediates that can attract bacteria having the ability of chemotaxis. Click here to learn more about root exudates. E.coli has five kinds of chemoreceptors, which interact with factors of the flagella that leads to chemotaxis. But E.coli doesn’t have specific chemotaxis towards some TCA intermediates while Pseudomonas putida has some McpS, like McfQ and McfR. We made a part BBa- containing the sequence of McfR, which detects succinate, malate and fumarate. Then we detected its chemotaxis towards malate and succinate, you can download our protocol which is based on the work 2011_Imperial_College_London had done before.click here to see the results. At last, we designed a model to mimic the movement pattern and predict the efficiency of the Prometheus E.coli.
Root exudates
Plants secrete both high- and low-molecular weight compounds from their roots, and these root exudates play an important role not only as nutrients for soil microbes but also as signal molecules in plant–microbe interactions (Sugiyama & Yazaki). In the wild, legume plants establish symbiotic interactions with rhizobia and arbuscular mycorrhizal fungi to obtain several nutrients such as nitrogen and phosphate. The root exudates of legume plants contain organic acids, including some TCA intermediates, such as malate, succinate, citrate and fumarate. Especially, in response to phosphorus starvation, malonie, succinic, fumaric, malic, citric, and t-aconitic acids were detected in the root exudates(Ohwaki & Hirata, 1992). Here, we design the Prometheus E.coli that responses to malate and succinate and will swim to the roots to improve the interaction between the roots and fungi.
Chemoreceptor and Chemotaxis
In isotropic chemical environments, E. coli swims in a random - walking pattern produced by alternating episodes of counter-clockwise (CCW) and clockwise (CW) flagellar rotation (Fig. 1, left panel). While an attractant or repellent appear somewhere in the environment, the cells’ locomotor responses specific runs that take the cells in favorable directions (toward attractants and away from repellents), resulting in net movement towards preferred environments. (Fig. 1, right panel).
Fig. 1 Random and biased walks. Left: A random walk in isotropic environments. When the cell's motors rotate CCW, the flagellar filaments push the cell forward. When one or more of the flagellar motors reverses to CW rotation, that filament undergoes a shape change (owing to the torque reversal) that disrupts the bundle. Until all motors once again turn in the CCW direction, the filaments act independently to push and pull the cell in a chaotic tumbling motion. Tumbling episodes enable the cell to try new, randomly-determined swimming directions. Right: A biased walk in a chemoeffector gradient. As cells swim up a concentration gradient of attractant, they spend more time smooth swimming than tumbling; this modulation of swimming behavior is manifested as a chemotactic response.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
E. coli has five chemoreceptors, four are methyl-accepting chemotaxis proteins (McpS) which have periplasmic ligand binding sites and conserved cytoplasmic signaling domains (Fig. 2). The McpS initiate a motor control response and a feedback circuit that updates the methylation record to achieve sensory adaptation and cessation of the motor response. A fifth MCP-like protein, Aer, mediates methylation-independent aeroTCAtic responses by monitoring redox changes in the electron transport chain. The five MCP-family receptors in E. coli utilize a common set of cytoplasmic signaling proteins to control flagellar rotation and sensory adaptation (Fig. 2). CheW and CheA generate receptor signals; CheY and CheZ modulate rotation of the flagellar motor and thus change cell behavior and movement; CheR and CheB regulate MCP methylation state to make feedback to CheW and CheA.
Fig. 2 Signaling components and circuit logic. E.coli receptors employ a common set of cytoplasmic signaling proteins: CheW and CheA interact with receptor molecules to form stable ternary complexes that generate stimulus signals; CheY transmits those signals to the flagellar motors, CheZ controls their lifetime; CheR (methyltransferase) and CheB (methylesterase) regulate MCP methylation state. Abbreviations: OM (outer membrane); PG (peptidoglycan layer of the cell wall); CM (cytoplasmic membrane).
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
But the original chemoreceptors of E.coli do not respond to the root exudates, while the McpS of the Pseudomonas putida , McfQ and McfR do(Parales, et al.). McfQ responds to citrate and fumarate, and McfR detects succinate, malate and fumarate. To compare with the work what 2011_Imperial_College_London had done, we chose McfR which also responds to malate. The mechanisms of prokaryote chemoreceptors are similar, so we designed a plasmid to express chemoreceptor. McfR in the E.coli makes the bacteria have the ability of chemotaxis towards TCA intermediates. As our experimental condition is limited, we just did experiments on chemotaxis towards succinate and malate. What’s more, in an attractant gradient, the chemoreceptors monitor chemoeffector concentration changes as they move around. And they use that information to modulate the probability of the next tumbling event. And we searched the pattern of their chemotaxis towards a concentration gradient of attractant using capillary assay. The results are demonstrated below.
Results
We did both agar assay and capillary assay to detect the response of E.coli to different attractants and different concentrations of each attractant. Because the agar assay (Fig.3) is difficult to replicate and collect the data from, we just show the results of capillary assay (Fig.4) . We made a negative control using washing buffer and five concentration gradients (100mM/10mM/1mM/0.01mM/0.0001mM) of attractants. These E.colis were divided into three groups based on the plasmid they have been transformed into. The plasmids are biobricks, BBa_K608003 and BBa_K515102 (they are from 5A and 8F wells in plate1), and the McfR plasmid was designed by us. BBa_K608003 (5A) only has a strong promoter and medium RBS, so it doesn’t have specific chemotaxis towards TCA intermediates. BBa_K515102 (8F) is a biobrick from 2011_Imperial_College_London, which responds to L(-)malic acid (HO2CCH2CH(OH)CO2H).
Fig.3 Agar assay: The three plates shows the chemotaxis results of 8F towards three kinds of attractants, malate, citrate and succinate from left to right. The filter paper of attractants is put on the left, the PBS is put on the right, bacteria is in the middle. Here, 8F swims fastest to malate.
Fig.4 E. coli’s ability of chemotaxis towards different concentrations of succinate or malate.
The cells were diluted 20000 times. 5A is a control which doesn’t have chemotaxis towards malate or succinate.
Malate: 8F showed the strongest respond. The tendency of curve of 8F was biphasic with maximums at attractant concentration of about 10-2 M and 10-5 M, and reached minimum at attractant concentration of about 10-1 M, which is similar to others’ work. With attractant concentration decreasing for 8F, the number of cells decreased slowly. McfR stayed stable at range of 10-7 M to 10-3 M, and had only one phase which reached its maximum at attractant concentration of 10-2 M, then it went down sharply at 10-1 M. There was a significant difference among 8F and 5A (p < 0.05), and quantity of cells of 8F was much more than that of 5A. So 8F has chemotaxis towards malate. On the other hand, McfR and 5A were not significantly different and quantity of cells of McfR was little less than it of 5A. So McfR shows no chemotaxis towards malate here.
Succinate: The tendencies of curves of 8F and McfR towards succinate are same. As the attractant concentration increased, the number of cells arose and reached the maximum at attractant concentration of about 10-2 M and fell sharply with the minimum at attractant concentration of 10-1 M. The quantities of cells of 8F and McfR were almost equivalent and did not have significant difference. But there were significant differences among 8F & 5A, and McfR & 5A: the number of cells of 5A are far less than 8F or McfR (p < 0.05), which demonstrated that 8F and McfR have chemotaxis towards succinate and the capacity of chemotaxis of 8F and McfR towards succinate are almost equal. Compared with chemotaxis towards malate, both of 8F and McfR show stronger chemotaxis towards succinate.
Analysis
The tendency of the chemotaxis towards chemical gradient may be influenced by two factors: pH and phosphorylation state of McpS. The motor of flagella is energized by a H＋ (or Na＋ in some species) gradient across the cytoplasmic membrane(Schmitt, 2003), but the mechanism is not clear. Lisa M. Maurer and Elizabeth Yohannes proved that low pH (at pH 5.0) induced the expression of some flagellar and chemotaxis genes and proton export, while coinducing oxidative stress and heat shock regulons to maintain internal pH homeostasis and to prepare the cell to survive future exposure to more extreme pH conditions (below pH 5 or above pH 9 which is higher or lower than the cytoplasmic pH 7.6)(Maurer, Yohannes, Bondurant, Radmacher, & Slonczewski, 2005). The pH of attractants showed below (Fig.5) is at the range of pH 1.0 – 6.4. The highest concentration of 0.1M is pH 1.0 of malate and 2.0 of succinate, which leads to weakest chemotaxis, for oxidative stress induces its protective responses more than chemotaixs genes expression; while the curves reach maximum at concentration of 0.01M because of the opposite reason.
Fig.5 The pH of the concentration gradients of malate and succinate. The pH of malate is lower than succinate at high concentration (10-1 and 10-2 M), and is equal with succinate at lower concentration. Both of them remain pH 6.4 at low concentration(10-5, 10-7 and 0 M).
On the other hand, the E. coli chemotaxis pathway is influenced by reversible McpS methylation and related proteins phosphorylation (Fig. 6). McpS, in response to chemoeffector stimuli, transfer the signals and make CheA autophosphorylated via the adapter protein CheW. Then phospho-CheA molecules serve as donors that transfer phosphoryl groups to specific aspartate residues in CheY and CheB. Phospho-CheY enhances CW rotation of the flagellar motors; phospho-CheB has high MCP methylesterase activity that helps to change the CW rotation to CCW rotation, and they will be inactive because of loss of phosphoryl group through spontaneous self-hydrolysis. CheZ further enhances the dephosphorylation rate of phospho-CheY to ensure rapid locomotor responses to changes in the supply of signaling phosphoryl groups to CheY. The signaling activities of chemoreceptors have two-state corresponding to two movement patterns separately (Fig. 6). Receptor complexes in the CW signaling state activate CheA, producing high levels of phospho-CheY. Receptors in the CCW signaling state deactivate CheA, resulting in low levels of phospho-CheY. Thus, the behavior of the flagellar motors reflects the relative proportion of receptor signaling complexes in the kinase-on and kinase-off conformations. For example, attractant ligands drive receptors toward the kinase-off state; subsequent addition of methyl groups shift receptors toward the kinase-on state, reestablishing the steady-state (adapted) balance between the two states and restoring random walk movements.
Fig. 6 Chemotaxis pathway. Reactions and components that augment CW rotation are depicted in green; those that augment CCW rotation are depicted in red.
Left: The flagellar motors of E. coli spin CCW by default of Che-Y; the signaling pathway modulates the level of phospho-CheY, the signal for CW rotation.
Right: The cartoons depict receptor ternary complexes in kinase-active (on) and kinase-inactive (off) signaling states. Changes in chemoeffector occupancy drive the complexes toward one state or the other. During sensory adaptation, changes in receptor methylation level shift signaling complexes toward the opposing state to restore a balance between CCW and CW signal outputs. The actual stoichiometry and structure of receptor signaling complexes are not known. Note that receptor methyl groups are attached to specific glutamic acid (E) residues in the MCP cytoplasmic domain, forming glutamyl methyl esters and neutralizing the negative charge on the glutamyl carboxyl group. Charge neutralization probably plays an important role in controlling receptor output state.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
Compared with the work of 2011_Imperial_College_London had done, we find that both of their biobrick BBa_K515102 and our biobrick BBa_K1405004 (originally found in P. aeruginosa and P. putida separately) have chemotaxis towards two kinds of TCA intermediates, malate and succinate (Fig.7 A). Estela Pineda-Molina, et al. reported high-resolution structures of the ligand- binding region of the cluster II McpS chemotaxis receptor (McpS-LBR) of Pseudomonas putida KT2440 in complex with malate and succinate (Fig.7 B& C) . The root mean square deviation (rmsd) between the malate and succinate cocrystal structure is only 0.2 Å indicating that differences in the nature of the ligand do not significantly alter the protein structure (Table 1). In a sequence alignment of McpS-LBR homologs containing McpS-LBR of Pseudomonas aeruginosa, the amino acids involved in malate and succinate binding are conserved. R60 is almost fully conserved, whereas the remaining residues are conserved to between 30–80% (Estela Pineda-Molina, et al.)
Table 1. Properties of the model
Fig.7 (A) The structure of malate and succinate, and the thermodynamic parameters for the 2 compounds that were found to bind. (B and C) View of the interaction of malate (B) and succinate (C) with the McpS-LBR. Malate binds to a cavity formed by α1 and the C-terminal segment of α6, and its coordination is achieved through interactions with R60, R63, R254, and T258 from one monomer and Q65 from the other monomer. Residues R60, R63, and Q65 form part of helix α1, whereas R254 and T258 are part of α6. Succinate binds to McpS-LBR in an almost identical manner as malate. Unlike malate, succinate has no hydroxyl group at C2. Therefore, the two hydrogen bonds that are established between the malate hydroxyl group, and the protein cannot be formed in the succinate structure. The remaining interactions of succinate with R60, R63, R254, and Q65 are analogous to the malate structure where they establish six hydrogen bonds.
Reference
Maurer, L. M., Yohannes, E., Bondurant, S. S., Radmacher, M., & Slonczewski, J. L. (2005). pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12. Journal of Bacteriology, 187(1), 304-319.
Ohwaki, Yoshinari, & Hirata, Hiroshi (1992). Differences in carboxylic acid exudation among P-starved leguminous crops in relation to carboxylic acid contents in plant tissues and phospholipid level in roots. Soil Science and Plant Nutrition, 38(2), 235-243.
Parales, Rebecca E, Luu, Rita A, Chen, Grischa Y, Liu, Xianxian, Wu, Victoria, Lin, Pamela, et al. Pseudomonas putida F1 has multiple chemoreceptors with overlapping specificity for organic acids. Microbiology, 159(Pt 6), 1086-1096.
Schmitt, R. (2003). Helix rotation model of the flagellar rotary motor. Biophysical Journal, 85(2), 843-852.
Sugiyama, Akifumi, & Yazaki, Kazufumi. Root exudates of legume plants and their involvement in interactions with soil microbes Secretions and exudates in biological systems (pp. 27-48): Springer.
Pineda-Molina, E., Reyes-Darias, J. A., Lacal, J., Ramos, J. L., García-Ruiz, J. M., Gavira, J. A., & Krell, T. (2012). Evidence for chemoreceptors with bimodular ligand-binding regions harboring two signal-binding sites. Proceedings of the National Academy of Sciences, 109(46), 18926-18931.
*You can download the protocol of this part here: Protocol on Delivery System.pdf
Overview
The plants root exudates contain TCA intermediates that can attract bacteria having the ability of chemotaxis. Click here to learn more about root exudates. E.coli has five kinds of chemoreceptors, which interact with factors of the flagella that leads to chemotaxis. But E.coli doesn’t have specific chemotaxis towards some TCA intermediates while Pseudomonas putida has some McpS, like McfQ and McfR. We made a part BBa- containing the sequence of McfR, which detects succinate, malate and fumarate. Then we detected its chemotaxis towards malate and succinate, you can download our protocol which is based on the work 2011_Imperial_College_London had done before.click here to see the results. At last, we designed a model to mimic the movement pattern and predict the efficiency of the Prometheus E.coli.
Root exudates
Plants secrete both high- and low-molecular weight compounds from their roots, and these root exudates play an important role not only as nutrients for soil microbes but also as signal molecules in plant–microbe interactions (Sugiyama & Yazaki). In the wild, legume plants establish symbiotic interactions with rhizobia and arbuscular mycorrhizal fungi to obtain several nutrients such as nitrogen and phosphate. The root exudates of legume plants contain organic acids, including some TCA intermediates, such as malate, succinate, citrate and fumarate. Especially, in response to phosphorus starvation, malonie, succinic, fumaric, malic, citric, and t-aconitic acids were detected in the root exudates(Ohwaki & Hirata, 1992). Here, we design the Prometheus E.coli that responses to malate and succinate and will swim to the roots to improve the interaction between the roots and fungi.
Chemoreceptor and Chemotaxis
In isotropic chemical environments, E. coli swims in a random - walking pattern produced by alternating episodes of counter-clockwise (CCW) and clockwise (CW) flagellar rotation (Fig. 1, left panel). While an attractant or repellent appear somewhere in the environment, the cells’ locomotor responses specific runs that take the cells in favorable directions (toward attractants and away from repellents), resulting in net movement towards preferred environments. (Fig. 1, right panel).
Fig. 1 Random and biased walks. Left: A random walk in isotropic environments. When the cell's motors rotate CCW, the flagellar filaments push the cell forward. When one or more of the flagellar motors reverses to CW rotation, that filament undergoes a shape change (owing to the torque reversal) that disrupts the bundle. Until all motors once again turn in the CCW direction, the filaments act independently to push and pull the cell in a chaotic tumbling motion. Tumbling episodes enable the cell to try new, randomly-determined swimming directions. Right: A biased walk in a chemoeffector gradient. As cells swim up a concentration gradient of attractant, they spend more time smooth swimming than tumbling; this modulation of swimming behavior is manifested as a chemotactic response.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
E. coli has five chemoreceptors, four are methyl-accepting chemotaxis proteins (McpS) which have periplasmic ligand binding sites and conserved cytoplasmic signaling domains (Fig. 2). The McpS initiate a motor control response and a feedback circuit that updates the methylation record to achieve sensory adaptation and cessation of the motor response. A fifth MCP-like protein, Aer, mediates methylation-independent aeroTCAtic responses by monitoring redox changes in the electron transport chain. The five MCP-family receptors in E. coli utilize a common set of cytoplasmic signaling proteins to control flagellar rotation and sensory adaptation (Fig. 2). CheW and CheA generate receptor signals; CheY and CheZ modulate rotation of the flagellar motor and thus change cell behavior and movement; CheR and CheB regulate MCP methylation state to make feedback to CheW and CheA.
Fig. 2 Signaling components and circuit logic. E.coli receptors employ a common set of cytoplasmic signaling proteins: CheW and CheA interact with receptor molecules to form stable ternary complexes that generate stimulus signals; CheY transmits those signals to the flagellar motors, CheZ controls their lifetime; CheR (methyltransferase) and CheB (methylesterase) regulate MCP methylation state. Abbreviations: OM (outer membrane); PG (peptidoglycan layer of the cell wall); CM (cytoplasmic membrane).
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
But the original chemoreceptors of E.coli do not respond to the root exudates, while the McpS of the Pseudomonas putida , McfQ and McfR do(Parales, et al.). McfQ responds to citrate and fumarate, and McfR detects succinate, malate and fumarate. To compare with the work what 2011_Imperial_College_London had done, we chose McfR which also responds to malate. The mechanisms of prokaryote chemoreceptors are similar, so we designed a plasmid to express chemoreceptor. McfR in the E.coli makes the bacteria have the ability of chemotaxis towards TCA intermediates. As our experimental condition is limited, we just did experiments on chemotaxis towards succinate and malate. What’s more, in an attractant gradient, the chemoreceptors monitor chemoeffector concentration changes as they move around. And they use that information to modulate the probability of the next tumbling event. And we searched the pattern of their chemotaxis towards a concentration gradient of attractant using capillary assay. The results are demonstrated below.
Results
We did both agar assay and capillary assay to detect the response of E.coli to different attractants and different concentrations of each attractant. Because the agar assay (Fig.3) is difficult to replicate and collect the data from, we just show the results of capillary assay (Fig.4) . We made a negative control using washing buffer and five concentration gradients (100mM/10mM/1mM/0.01mM/0.0001mM) of attractants. These E.colis were divided into three groups based on the plasmid they have been transformed into. The plasmids are biobricks, BBa_K608003 and BBa_K515102 (they are from 5A and 8F wells in plate1), and the McfR plasmid was designed by us. BBa_K608003 (5A) only has a strong promoter and medium RBS, so it doesn’t have specific chemotaxis towards TCA intermediates. BBa_K515102 (8F) is a biobrick from 2011_Imperial_College_London, which responds to L(-)malic acid (HO2CCH2CH(OH)CO2H).
Fig.3 Agar assay: The three plates shows the chemotaxis results of 8F towards three kinds of attractants, malate, citrate and succinate from left to right. The filter paper of attractants is put on the left, the PBS is put on the right, bacteria is in the middle. Here, 8F swims fastest to malate.
Fig.4 E. coli’s ability of chemotaxis towards different concentrations of succinate or malate.
The cells were diluted 20000 times. 5A is a control which doesn’t have chemotaxis towards malate or succinate.
Malate: 8F showed the strongest respond. The tendency of curve of 8F was biphasic with maximums at attractant concentration of about 10-2 M and 10-5 M, and reached minimum at attractant concentration of about 10-1 M, which is similar to others’ work. With attractant concentration decreasing for 8F, the number of cells decreased slowly. McfR stayed stable at range of 10-7 M to 10-3 M, and had only one phase which reached its maximum at attractant concentration of 10-2 M, then it went down sharply at 10-1 M. There was a significant difference among 8F and 5A (p < 0.05), and quantity of cells of 8F was much more than that of 5A. So 8F has chemotaxis towards malate. On the other hand, McfR and 5A were not significantly different and quantity of cells of McfR was little less than it of 5A. So McfR shows no chemotaxis towards malate here.
Succinate: The tendencies of curves of 8F and McfR towards succinate are same. As the attractant concentration increased, the number of cells arose and reached the maximum at attractant concentration of about 10-2 M and fell sharply with the minimum at attractant concentration of 10-1 M. The quantities of cells of 8F and McfR were almost equivalent and did not have significant difference. But there were significant differences among 8F & 5A, and McfR & 5A: the number of cells of 5A are far less than 8F or McfR (p < 0.05), which demonstrated that 8F and McfR have chemotaxis towards succinate and the capacity of chemotaxis of 8F and McfR towards succinate are almost equal. Compared with chemotaxis towards malate, both of 8F and McfR show stronger chemotaxis towards succinate.
Analysis
The tendency of the chemotaxis towards chemical gradient may be influenced by two factors: pH and phosphorylation state of McpS. The motor of flagella is energized by a H＋ (or Na＋ in some species) gradient across the cytoplasmic membrane(Schmitt, 2003), but the mechanism is not clear. Lisa M. Maurer and Elizabeth Yohannes proved that low pH (at pH 5.0) induced the expression of some flagellar and chemotaxis genes and proton export, while coinducing oxidative stress and heat shock regulons to maintain internal pH homeostasis and to prepare the cell to survive future exposure to more extreme pH conditions (below pH 5 or above pH 9 which is higher or lower than the cytoplasmic pH 7.6)(Maurer, Yohannes, Bondurant, Radmacher, & Slonczewski, 2005). The pH of attractants showed below (Fig.5) is at the range of pH 1.0 – 6.4. The highest concentration of 0.1M is pH 1.0 of malate and 2.0 of succinate, which leads to weakest chemotaxis, for oxidative stress induces its protective responses more than chemotaixs genes expression; while the curves reach maximum at concentration of 0.01M because of the opposite reason.
Fig.5 The pH of the concentration gradients of malate and succinate. The pH of malate is lower than succinate at high concentration (10-1 and 10-2 M), and is equal with succinate at lower concentration. Both of them remain pH 6.4 at low concentration(10-5, 10-7 and 0 M).
On the other hand, the E. coli chemotaxis pathway is influenced by reversible McpS methylation and related proteins phosphorylation (Fig. 6). McpS, in response to chemoeffector stimuli, transfer the signals and make CheA autophosphorylated via the adapter protein CheW. Then phospho-CheA molecules serve as donors that transfer phosphoryl groups to specific aspartate residues in CheY and CheB. Phospho-CheY enhances CW rotation of the flagellar motors; phospho-CheB has high MCP methylesterase activity that helps to change the CW rotation to CCW rotation, and they will be inactive because of loss of phosphoryl group through spontaneous self-hydrolysis. CheZ further enhances the dephosphorylation rate of phospho-CheY to ensure rapid locomotor responses to changes in the supply of signaling phosphoryl groups to CheY. The signaling activities of chemoreceptors have two-state corresponding to two movement patterns separately (Fig. 6). Receptor complexes in the CW signaling state activate CheA, producing high levels of phospho-CheY. Receptors in the CCW signaling state deactivate CheA, resulting in low levels of phospho-CheY. Thus, the behavior of the flagellar motors reflects the relative proportion of receptor signaling complexes in the kinase-on and kinase-off conformations. For example, attractant ligands drive receptors toward the kinase-off state; subsequent addition of methyl groups shift receptors toward the kinase-on state, reestablishing the steady-state (adapted) balance between the two states and restoring random walk movements.
Fig. 6 Chemotaxis pathway. Reactions and components that augment CW rotation are depicted in green; those that augment CCW rotation are depicted in red.
Left: The flagellar motors of E. coli spin CCW by default of Che-Y; the signaling pathway modulates the level of phospho-CheY, the signal for CW rotation.
Right: The cartoons depict receptor ternary complexes in kinase-active (on) and kinase-inactive (off) signaling states. Changes in chemoeffector occupancy drive the complexes toward one state or the other. During sensory adaptation, changes in receptor methylation level shift signaling complexes toward the opposing state to restore a balance between CCW and CW signal outputs. The actual stoichiometry and structure of receptor signaling complexes are not known. Note that receptor methyl groups are attached to specific glutamic acid (E) residues in the MCP cytoplasmic domain, forming glutamyl methyl esters and neutralizing the negative charge on the glutamyl carboxyl group. Charge neutralization probably plays an important role in controlling receptor output state.
The pictures are from Parkinson Lab - University of Utah ( The website address [http://chemotaxis.biology.utah.edu/Parkinson_Lab/projects/ecolichemotaxis/ecolichemotaxis.html])
Compared with the work of 2011_Imperial_College_London had done, we find that both of their biobrick BBa_K515102 and our biobrick BBa_K1405004 (originally found in P. aeruginosa and P. putida separately) have chemotaxis towards two kinds of TCA intermediates, malate and succinate (Fig.7 A). Estela Pineda-Molina, et al. reported high-resolution structures of the ligand- binding region of the cluster II McpS chemotaxis receptor (McpS-LBR) of Pseudomonas putida KT2440 in complex with malate and succinate (Fig.7 B& C) . The root mean square deviation (rmsd) between the malate and succinate cocrystal structure is only 0.2 Å indicating that differences in the nature of the ligand do not significantly alter the protein structure (Table 1). In a sequence alignment of McpS-LBR homologs containing McpS-LBR of Pseudomonas aeruginosa, the amino acids involved in malate and succinate binding are conserved. R60 is almost fully conserved, whereas the remaining residues are conserved to between 30–80% (Estela Pineda-Molina, et al.)
Table 1. Properties of the model
Fig.7 (A) The structure of malate and succinate, and the thermodynamic parameters for the 2 compounds that were found to bind. (B and C) View of the interaction of malate (B) and succinate (C) with the McpS-LBR. Malate binds to a cavity formed by α1 and the C-terminal segment of α6, and its coordination is achieved through interactions with R60, R63, R254, and T258 from one monomer and Q65 from the other monomer. Residues R60, R63, and Q65 form part of helix α1, whereas R254 and T258 are part of α6. Succinate binds to McpS-LBR in an almost identical manner as malate. Unlike malate, succinate has no hydroxyl group at C2. Therefore, the two hydrogen bonds that are established between the malate hydroxyl group, and the protein cannot be formed in the succinate structure. The remaining interactions of succinate with R60, R63, R254, and Q65 are analogous to the malate structure where they establish six hydrogen bonds.
Reference
Maurer, L. M., Yohannes, E., Bondurant, S. S., Radmacher, M., & Slonczewski, J. L. (2005). pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12. Journal of Bacteriology, 187(1), 304-319.
Ohwaki, Yoshinari, & Hirata, Hiroshi (1992). Differences in carboxylic acid exudation among P-starved leguminous crops in relation to carboxylic acid contents in plant tissues and phospholipid level in roots. Soil Science and Plant Nutrition, 38(2), 235-243.
Parales, Rebecca E, Luu, Rita A, Chen, Grischa Y, Liu, Xianxian, Wu, Victoria, Lin, Pamela, et al. Pseudomonas putida F1 has multiple chemoreceptors with overlapping specificity for organic acids. Microbiology, 159(Pt 6), 1086-1096.
Schmitt, R. (2003). Helix rotation model of the flagellar rotary motor. Biophysical Journal, 85(2), 843-852.
Sugiyama, Akifumi, & Yazaki, Kazufumi. Root exudates of legume plants and their involvement in interactions with soil microbes Secretions and exudates in biological systems (pp. 27-48): Springer.
Pineda-Molina, E., Reyes-Darias, J. A., Lacal, J., Ramos, J. L., García-Ruiz, J. M., Gavira, J. A., & Krell, T. (2012). Evidence for chemoreceptors with bimodular ligand-binding regions harboring two signal-binding sites. Proceedings of the National Academy of Sciences, 109(46), 18926-18931.
*You can download the protocol of this part here: Protocol on Delivery System.pdf
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The Story of E.coli Prometheus
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