Plant hormone sensing method using rare earth compounds, sensor using the same, and method for early detection of plant disease infection

Abstract

To provide a method for sensing methyl salicylate, which is a plant hormone released in disease infection in cultivation of plant, including agricultural crop and its sensor, and thereby to provide a method for plant disease infection early detection in situ.SOLUTION: A plant disease infections can be detected at an early stage by using, a rare earth compound that selectively recognizes methyl salicylate, which is a plant hormone released by plants at pathogen infection, and forms a complex as a sensing receptor and by using a fluorescent emission phenomenon and changes in electrochemical behavior after reaction with methyl salicylate.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a method for sensing plant hormones released when a plant is infected with a disease, and a method for early detection of disease infection in a plant. [Background technology]

[0002] Plants are known to have their own defense mechanisms in place when they are infected by pathogens such as fungi, herbivory by pests, or stressed by environmental changes. Specifically, when plants are infected by pathogens, they synthesize the signal substance salicylic acid at the site of infection. Salicylic acid then moves throughout the plant via the phloem tissue and induces defense mechanisms in uninfected tissues, resulting in systemic resistance to pathogens (systemic acquired resistance). Furthermore, when plants are herbivore-damaged by pests, they synthesize ethylene and jasmonic acid, which, like salicylic acid, move throughout the plant and induce defense mechanisms throughout the plant (induced systemic resistance). Furthermore, plants are known to adapt to environmental stresses such as drought, low temperatures, and salt damage by synthesizing abscisic acid.

[0003] It is also known that plants have a mechanism for informing not only themselves but also surrounding plants when they are infected with pathogens or damaged by pests (Non-Patent Document 1). Specifically, salicylic acid synthesized when infected by pathogens is methylated to form methyl salicylate, which is released from the plant as a volatile signal substance to notify surrounding plants of the pathogen infection and stimulate defense mechanisms in advance. It is also known that jasmonic acid synthesized when damaged by pests is methylated to form methyl jasmonate, a volatile signal that is released from the plant, inducing resistance in surrounding plants in advance.

[0004] It is known that plants release plant hormones as signal substances when they are damaged by pests and diseases, and by quickly sensing these signal substances, it is possible to detect pest damage early.

[0005] One method for early detection of damage by sensing jasmonic acid, which is released as a volatile signal when pests infest crops, is disclosed in Patent Document 1. This method involves cultivating a monitor plant carrying a photoprotein gene next to the crops being cultivated, and utilizing the phenomenon in which the monitor plant detects methyl jasmonate released when the crops are damaged by pests and emits light. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] WO2019 / 082942 publication [Non-patent literature]

[0007] [Non-Patent Document 1] J. Japan Association on Odor Environment, Vol.36, No.3, 153-155(2005). Summary of the Invention [Problem to be solved by the invention]

[0008] The present invention aims to provide a method for sensing methyl salicylate, a plant hormone released when plants, including agricultural crops, become infected with a disease during cultivation, and a sensor for the same, thereby providing a method for detecting disease infection in plants at an early stage and on site. [Means for solving the problem]

[0009] The present invention is characterized by utilizing a rare earth compound as a sensor receptor, which selectively recognizes the volatile plant hormone methyl salicylate to form a complex. The present invention is also characterized by utilizing the fluorescence emission phenomenon of the complex formed by the reaction of methyl salicylate with a rare earth compound, thereby enabling early detection of plant disease infection. Furthermore, the present invention is characterized by utilizing the phenomenon in which the electrochemical behavior changes upon reaction of methyl salicylate with a rare earth compound, thereby enabling early detection of plant disease infection. [Effects of the Invention]

[0010] By using the rare earth compound of the present invention as a sensor receptor, it is possible to selectively sense methyl salicylate, a volatile plant hormone released when plants are infected with pathogenic bacteria.Furthermore, by utilizing the fluorescence emission phenomenon from the complex formed by the reaction of methyl salicylate with the rare earth compound, or by utilizing changes in electrochemical behavior, it is possible to detect plant infection by pathogenic bacteria at an early stage. [Brief explanation of the drawings]

[0011] [Figure 1] 1 is a photograph confirming fluorescence emission in Example 1. [Figure 2] 1 is a photograph confirming fluorescence emission in Comparative Example 1. [Figure 3] 10 is a photograph confirming fluorescence emission in Example 2. [Figure 4] 10 is a photograph confirming fluorescence emission in Example 3. [Figure 5] 10 is a photograph confirming fluorescence emission in Example 4. [Figure 6] 10 is a photograph confirming fluorescence emission in Comparative Example 2. [Figure 7] 10 is a photograph confirming the fluorescence emission obtained in Example 5. [Figure 8] 10 is a photograph confirming the fluorescence emission obtained in Comparative Example 3. [Figure 9] 10 is a photograph confirming the fluorescence emission obtained in Example 6. [Figure 10] 10 is a photograph confirming the fluorescence emission obtained in Comparative Example 4. [Figure 11] 1 is a photograph confirming the fluorescence obtained in Example 7. [Figure 12] 10 is a photograph confirming the fluorescence emission obtained in Comparative Example 5. [Figure 13] 10 is a photograph confirming the fluorescence emission obtained in Example 8. [Figure 14] 10 is a photograph confirming the fluorescence emission obtained in Example 9. [Figure 15] 1 is a fluorescence spectrum curve obtained in Example 10. [Figure 16] 10 is a photograph confirming the fluorescence obtained in Example 11. [Figure 17] 10 is a photograph confirming the fluorescence obtained in Example 12. [Figure 18] 10 is a fluorescence spectrum curve in Example 13. [Figure 19] 1 is a graph plotting the fluorescence intensity obtained in Example 13. [Figure 20] 1 is a graph showing the current-voltage curve (cyclic voltammogram) obtained in Example 14. [Figure 21] 1 is a fluorescence spectrum curve obtained in Example 15. DETAILED DESCRIPTION OF THE INVENTION

[0012] Hereinafter, embodiments for carrying out the present invention will be described with reference to the drawings, etc. However, although the embodiments described below have technically preferable limitations for carrying out the present invention, the scope of the invention is not limited to the following.

[0013] The present inventors have conducted extensive research to solve the above-mentioned problems, and as a result have discovered that methyl salicylate, a volatile signal substance released by plants when infected with pathogenic bacteria, can be selectively sensed using rare earth compounds, thereby completing the present invention.

[0014] The present embodiment will be described in detail below.

[0015] <Methyl salicylate receptor: rare earth compounds> Rare earth compounds that can be used as receptors for sensing methyl salicylate include salts of rare earth elements, such as salts of scandium (Sc), yttrium (Y), lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu), particularly acetates, chlorides, oxalates, nitrates, propionates, isobutyrates, and pivalates. Specific examples include scandium acetate hydrate, yttrium acetate tetrahydrate, lanthanum acetate hydrate, cerium acetate monohydrate, praseodymium acetate monohydrate, neodymium acetate monohydrate, samarium acetate hydrate, europium acetate hydrate, gadolinium acetate tetrahydrate, terbium acetate tetrahydrate, dysprosium acetate tetrahydrate, holmium acetate tetrahydrate, erbium acetate tetrahydrate, thulium acetate tetrahydrate, ytterbium acetate tetrahydrate, lutetium acetate tetrahydrate, europium chloride hexahydrate, terbium chloride hexahydrate, dysprosium chloride hexahydrate, terbium nitrate hexahydrate, terbium oxalate decahydrate, terbium propionate, terbium isobutyrate, and terbium pivalate, but are not limited to these.

[0016] For example, terbium acetate can selectively recognize methyl salicylate by forming a complex with methyl salicylate through the reaction shown in formula (1) below.

[0017] [ka]

[0018] Also useful are compounds in which a salt of a rare earth element forms a complex with a phosphine oxide derivative. Examples of the phosphine oxide derivative include, but are not limited to, triphenylphosphine oxide, tributylphosphine oxide, trihexylphosphine oxide, tricyclohexylphosphine oxide, tris(4-methoxyphenyl)phosphine oxide, 4-(dimethylamino)phenyldiphenylphosphine oxide, tri(2-thienyl)phosphine oxide, 1,3-bis(diphenylphosphino)propane dioxide, 1,4-bis(diphenylphosphino)butane dioxide, bis[2-(diphenylphosphino)phenyl]ether dioxide, and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene dioxide. These phosphine oxide derivatives of rare earth element salts are synthesized by reacting the rare earth element salt with phosphine oxide in methanol under heating. For example, as shown in the following formula (2), a complex of terbium acetate and triphenylphosphine oxide is synthesized by heating and refluxing terbium acetate and triphenylphosphine oxide in methanol for 4 hours.

[0019] [ka] The complex of terbium acetate and phosphine oxide can selectively recognize methyl salicylate by forming a complex with methyl salicylate through the reaction shown in formula (3) below.

[0020] [ka]

[0021] Thus, some embodiments of the present invention relate to a method for detecting methyl salicylate, comprising reacting a rare earth compound with methyl salicylate to form a complex.

[0022] Furthermore, some embodiments of the present invention relate to a method for sensing methyl salicylate, which is characterized by using a rare earth compound as a receptor that selectively recognizes methyl salicylate.

[0023] In some embodiments, the rare earth compound may be terbium(III) acetate tetrahydrate, in some embodiments, dysprosium(III) acetate tetrahydrate, or gadolinium(III) acetate tetrahydrate.

[0024] In some embodiments, the reaction of the rare earth compound with methyl salicylate is carried out in a solution, which may be, for example, but not limited to, a dimethyl sulfoxide solution, a methanol solution, or an aqueous solution. , rare The concentration of the earth compound can be, for example, in the range of 0.00001 mol / L to 5 mol / L, for example, in the range of 0.00004 mol / L to 1 mol / L.

[0025] In some embodiments, the reaction of the rare earth compound with methyl salicylate is carried out in a solid medium containing the rare earth compound. The solid medium can be, for example, paper or glass (e.g., glass fiber, porous glass substrate, etc.), or a resin (e.g., polymethyl methacrylate, polyethylene, polypropylene, polyvinyl chloride, polystyrene, nylon resin, polyamide, polycarbonate, polyethylene terephthalate, polybutylene terephthalate, polyphenylene oxide, water-soluble polymers (cellulose-based, agarose, starch-based, sodium alginate, acrylic acid-based, acrylamide-based, polyvinyl alcohol, polyethylene oxide, polyvinylpyrrolidone, etc.), but is not limited to these.

[0026] <Fluorescence phenomenon> The complex formed by the reaction of rare earth compounds with methyl salicylate emits new fluorescence. Specifically, when the complex formed by the reaction of rare earth compounds with methyl salicylate is irradiated with excitation light with a wavelength of 200 to 400 nm, it emits fluorescence. On the other hand, the rare earth compound alone hardly emits fluorescence, which makes it possible to detect methyl salicylate.

[0027] Therefore, some embodiments of the present invention relate to a method for detecting methyl salicylate, including the steps of (i) reacting a rare earth compound with methyl salicylate to form a complex, (ii) irradiating the complex with excitation light, and (iii) detecting fluorescence emitted by the complex. In some embodiments, an appropriate excitation wavelength within the range of 200 to 400 nm is selected. Furthermore, in some embodiments, a step of determining the concentration of methyl salicylate by comparing the intensity of the detected fluorescence with a predetermined reference value may also be performed.

[0028] Furthermore, some embodiments of the present invention relate to a method for sensing methyl salicylate, which utilizes the phenomenon in which methyl salicylate reacts with a rare earth compound to form a rare earth complex, thereby emitting fluorescence.

[0029] <Electrochemical behavior> The complex formed by the reaction of rare earth compounds with methyl salicylate exhibits electrochemical behavior different from that of the receptor rare earth compounds. Specifically, cyclic voltammetry measurements of an electrochemical cell containing a complex of rare earth compounds and methyl salicylate show a large change in current value around a specific potential. This makes it possible to detect methyl salicylate by monitoring this current value.

[0030] Some embodiments of the present invention relate to a method for detecting methyl salicylate, including (i) reacting a rare earth compound with methyl salicylate in a solution to form a complex, (ii) measuring the current flowing under a constant voltage, and (iii) detecting a change in the current value resulting from the formation of the complex. In some embodiments, the voltage is selected to be an appropriate value within the range of −1 to 2 V (vs. a normal hydrogen electrode (NHE)). The solution may contain, but is not limited to, tetrabutylammonium perchlorate as a supporting electrolyte. Furthermore, in some embodiments, a step of determining the concentration of methyl salicylate by comparing the detected change in the current value with a predetermined reference value may also be performed.

[0031] Furthermore, some embodiments of the present invention relate to a method for sensing methyl salicylate, which utilizes the phenomenon that rare earth compounds react with methyl salicylate to form a complex, and the electrochemical behavior of the complex differs from that of the rare earth compounds.

[0032] Furthermore, some embodiments of the present invention relate to a method for sensing methyl salicylate, which utilizes the phenomenon that a rare earth compound reacts with methyl salicylate to form a complex, and the current value of the complex in a certain potential region is different from that of the rare earth compound.

[0033] In some embodiments, the methyl salicylate sensing method of the present invention can be used for detecting pathogen infection of agricultural crops.

[0034] <Methyl salicylate sensor> The methyl salicylate sensor of the present invention, which uses a rare earth compound as a receptor, is composed of at least a recognition unit for methyl salicylate and a detection unit that detects the recognition of methyl salicylate by the recognition unit. The recognition unit contains at least a rare earth compound as a receptor. The rare earth compound does not react with or recognize plant hormones other than methyl salicylate, such as methyl jasmonate, and is therefore capable of selectively recognizing methyl salicylate. The detection unit is configured to optically and / or electrochemically detect the recognition of methyl salicylate by the methyl salicylate recognition unit. For example, the optical detection unit is composed of at least an excitation light source and a detection element to detect the fluorescence emission of the complex formed between the rare earth compound and methyl salicylate, and detects and measures the concentration of methyl salicylate based on changes in fluorescence intensity. Furthermore, in the electrochemical detection section, in order to detect changes in electrochemical behavior, an electrochemical cell (detection element) having electrodes is constructed so as to detect the current generated by the oxidation-reduction reaction of the complex formed by the reaction of the rare earth compound with methyl salicylate, and the change in the electrochemical behavior of the electrochemical cell (for example, the change in the current value at a certain potential) is used to detect methyl salicylate and measure its concentration.

[0035] Thus, some embodiments of the present invention relate to a methyl salicylate sensor for detecting methyl salicylate, comprising at least a methyl salicylate recognition unit having a rare earth compound as a receptor that selectively recognizes methyl salicylate, and a detection unit that detects the recognition of methyl salicylate by the recognition unit. In some embodiments, the methyl salicylate sensor of the present invention detects methyl salicylate, a plant hormone released when agricultural crops are infected with pathogenic bacteria. Thus, the methyl salicylate sensor of the present invention can be used as a sensor for detecting pathogenic bacteria infection in agricultural crops. In some embodiments, the methyl salicylate sensor of the present invention can selectively detect methyl salicylate over methyl jasmonate.

[0036] Some embodiments of the present invention relate to a methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for optically detecting the recognition of methyl salicylate by the recognition unit. In some embodiments, the optical detection unit includes at least an excitation light source and a detection element. In some embodiments, the methyl salicylate sensor of the present invention can detect and / or measure the concentration of methyl salicylate based on changes in observed fluorescence intensity.

[0037] Furthermore, some embodiments of the present invention relate to a methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for electrochemically detecting the recognition of methyl salicylate by the recognition unit. In some embodiments, the electrochemical detection unit includes an electrochemical cell having electrodes for detecting a current generated by a redox reaction of a complex formed between the rare earth compound and methyl salicylate. In some embodiments, the methyl salicylate sensor of the present invention can detect and / or measure the concentration of methyl salicylate based on changes in the current value of the electrochemical cell.

[0038] In some embodiments, the detection unit may include a computer executing a program for processing the detection and / or concentration measurement of methyl salicylate. Such a program may, for example, cause the computer to receive signals from the optical and / or electrochemical detection element, analyze the received signals to determine the presence and / or concentration of methyl salicylate, and output the analysis results. In some embodiments, analyzing the received signals may include, for example, determining the presence and / or concentration of methyl salicylate by comparing the received signals with predetermined reference values. In some embodiments, the analysis results may be output, for example, to a display device connected to the sensor or to another device connected via a network.

[0039] Therefore, some embodiments of the present invention relate to a methyl salicylate sensor for detecting methyl salicylate, comprising at least a methyl salicylate recognition unit having a rare earth compound as a receptor that selectively recognizes methyl salicylate, and a detection unit that detects recognition of methyl salicylate by the recognition unit, wherein the detection unit includes a detection element and a computer, and the computer has a program that causes it to execute the steps of: (i) receiving a signal from the optical and / or electrochemical detection element; (ii) analyzing the received signal to determine the presence or absence and / or concentration of methyl salicylate; and (iii) outputting the analysis results.

[0040] <Method for early detection of pathogenic fungal infection in agricultural crops> One application of the methyl salicylate sensor of the present invention is to install the methyl salicylate sensor near planted crops and detect methyl salicylate with the sensor, thereby enabling early detection of pathogenic fungal infection of the crops.

[0041] Thus, some embodiments of the present invention relate to a method for detecting pathogen infection of agricultural crops by placing a methyl salicylate sensor near the crops and detecting methyl salicylate with the sensor. In some embodiments, the methyl salicylate sensor is characterized by comprising at least a methyl salicylate recognition unit having a rare earth compound as a receptor that selectively recognizes methyl salicylate, and a detection unit that detects recognition of methyl salicylate by the recognition unit. In some embodiments, the methyl salicylate sensor is characterized by comprising at least (i) a methyl salicylate recognition unit having a rare earth compound, and (ii) a detection unit that optically and / or electrochemically detects recognition of methyl salicylate by the recognition unit.

[0042] Examples of crops that may be monitored include, but are not limited to, cucumbers, watermelons, tomatoes, eggplants, bell peppers, paprika, shishito peppers, melons, Chinese cabbage, cabbage, radishes, lettuce, leeks, broccoli, onions, garlic, yams, asparagus, carrots, potatoes, celery, tobacco, rice, and strawberries.

[0043] Diseases that can be detected include, but are not limited to, ring spot, white spot, brown ring spot, downy mildew, wilt, root rot wilt, half-leaf wilt, brown root rot, gray blight, root rot, black spot root rot, southern blight, damping-off, brown spot, downy mildew, powdery mildew, gray mold, anthracnose, black spot, sclerotinia, vine blight, spot, late blight, mosaic disease, yellow necrosis, yellow cigar disease, bacterial wilt, soft rot, canker, bacterial stem necrosis, bacterial black spot, and bacterial spot. Pathogenic infections that can be detected include, but are not limited to, infections by the causative fungi of the above diseases.

[0044] In the context of the present disclosure, when a sensor is installed near a crop, examples of the term "nearby" include, but are not limited to, a distance of within 2 m, within 1 m, within 75 cm, within 50 cm, within 40 cm, within 30 cm, within 20 cm, within 10 cm, or within 5 cm from the crop to be monitored, and an appropriate distance is appropriately selected taking various factors into consideration. A person skilled in the art would be able to appropriately determine the location to install the sensor taking various conditions into consideration.

[0045] Furthermore, some embodiments of the present invention relate to the use of a methyl salicylate sensor in detecting pathogen infection in agricultural crops. Also, some embodiments of the present invention relate to the use of rare earth compounds in the manufacture of a methyl salicylate sensor. [Example]

[0046] The present invention will be explained in more detail below by way of examples, but the present invention is not limited to these examples.

[0047] Example 1 A 0.2 ml solution of 0.05 g of terbium(III) acetate tetrahydrate (TbA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain filter paper containing TbA. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 1(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl salicylate (MSA), which is released when plants are infected with pathogenic fungi, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 1(b)). The results showed that TbA does not emit fluorescence on its own, but reacts with methyl salicylate to emit fluorescence, demonstrating its ability to sense methyl salicylate.

[0048] (Comparative Example 1) A 0.2 ml solution of 0.05 g of terbium(III) acetate tetrahydrate (TbA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain filter paper containing TbA. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 2(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl jasmonate, a signal substance released by plants when damaged by pests, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 2(b)). The results showed that TbA did not react with methyl jasmonate and did not emit fluorescence.

[0049] The results of Example 1 and Comparative Example 1 demonstrate that TbA can selectively sense methyl salicylate, which is released by plants when infected with pathogenic bacteria.

[0050] Example 2 A 0.2 ml solution of 0.05 g of terbium(III) acetate tetrahydrate (TbA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and allowed to dry, yielding a filter paper containing TbA. Next, this filter paper and 0.05 g of methyl salicylate were placed in a petri dish and stored in a desiccator, avoiding direct contact. After one hour, the filter paper was removed and excited with a UV lamp (wavelength 365 nm) to evaluate for fluorescence. Yellow-green fluorescence was confirmed (Figure 3). These results demonstrate that the methyl salicylate released by plants upon pathogen infection can be sensed as a volatile signal.

[0051] Example 3 Terbium(III) acetate tetrahydrate (TbA) (0.1 g) and polymethyl methacrylate (PMMA) (0.1 g) were dissolved in 2 ml of dimethyl sulfoxide. The solution was then spin-coated onto a circular glass substrate (30 mm diameter) and dried on a hot plate at 90 °C for 5 min to obtain a TbA-containing PMMA coating film. The resulting glass substrate was excited with a UV lamp (365 nm wavelength) to check for fluorescence, but no fluorescence was observed (Figure 4(a)). The glass substrate and 0.05 g of methyl salicylate were then placed in a Petri dish and stored in a desiccator without direct contact. After 21 h, the glass substrate was removed and excited with a UV lamp (365 nm wavelength) to check for fluorescence. Yellow-green fluorescence was observed (Figure 4(b)). These results demonstrate that TbA can sense methyl salicylate, a volatile signal released by plants during pathogen infection.

[0052] Example 4 A 0.2 ml solution of 0.2 g of gadolinium(III) acetate tetrahydrate (GdA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain filter paper containing GdA. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 5(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl salicylate (MSA), which is released when plants are infected with pathogenic bacteria, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 5(b)). The results showed that GdA does not emit fluorescence on its own, but reacts with methyl salicylate to emit fluorescence, demonstrating its ability to sense methyl salicylate.

[0053] (Comparative Example 2) A 0.2 ml solution of 0.2 g of gadolinium(III) acetate tetrahydrate (GdA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain filter paper containing GdA. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 6(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl jasmonate, a signal substance released by plants when damaged by pests, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 6(b)). The results showed that GdA did not react with methyl jasmonate and did not emit fluorescence.

[0054] The results of Example 4 and Comparative Example 2 demonstrate that GdA can selectively sense methyl salicylate, which is released by plants when infected with pathogenic bacteria.

[0055] Example 5 A solution of samarium(III) acetate hydrate (SmA) was prepared by dissolving 0.1 g of SmA in 3 ml of dimethyl sulfoxide (DMSO). Next, 0.2 ml of an MSA solution in acetonitrile (0.1 mol / L) was added to 1.5 ml of the SmA solution to prepare an SmA solution containing MSA. The two resulting solutions were excited with a UV lamp (wavelength 365 nm) to confirm whether they emitted fluorescence (Figure 7). As a result, no fluorescence was observed in the solution containing only SmA (a), but the solution containing MSA (b) exhibited the red fluorescence characteristic of samarium complexes, demonstrating its ability to sense methyl salicylate.

[0056] (Comparative Example 3) A samarium(III) acetate hydrate (SmA) solution was prepared by dissolving 0.1 g of SmA in 3 ml of DMSO. Next, 0.2 ml of a 0.1 mol / L solution of methyl jasmonate (MJA) in acetonitrile was added to 1.5 ml of the SmA solution to prepare an SmA solution containing MJA. The two resulting solutions were excited with a UV lamp (wavelength 365 nm) to confirm whether they emitted fluorescence (Figure 8). Neither the solution containing SmA alone (a) nor the solution containing MJA (b) emitted fluorescence.

[0057] The results of Example 5 and Comparative Example 3 demonstrate that SmA can selectively sense methyl salicylate, which is released by plants when infected with pathogenic bacteria.

[0058] Example 6 A 0.2 ml solution of 0.2 g of dysprosium(III) acetate tetrahydrate (DyA) dissolved in 2 ml of methanol was dropped onto a circular filter paper (45 mm diameter) and dried to obtain DyA-containing filter paper. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 9(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl salicylate (MSA), which is released when plants are infected with pathogenic bacteria, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 9(b)). The results showed that DyA does not emit fluorescence on its own, but reacts with methyl salicylate to emit yellow fluorescence, demonstrating its ability to sense methyl salicylate.

[0059] Comparative Example 4 0.2 g of dysprosium(III) acetate tetrahydrate (DyA) was dissolved in 2 mL of methanol, and 0.2 mL of this solution was dropped onto a circular filter paper (45 mm diameter) and dried to obtain DyA-containing filter paper. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence (Figure 10(a)). Next, 0.03 mL of an acetonitrile solution (0.1 mol / L) of methyl jasmonate, a signal substance released by plants when damaged by pests, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence (Figure 10(b)). The results showed that DyA did not react with methyl jasmonate and did not emit fluorescence (Figure 10(b)).

[0060] The results of Example 6 and Comparative Example 4 demonstrate that DyA can selectively sense methyl salicylate, which is released by plants when infected with pathogenic bacteria.

[0061] Example 7 A 0.2 ml solution of 0.05 g of terbium(III) chloride hexahydrate (TbC) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain TbC-containing filter paper. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence emission (Figure 11(a)). Next, 0.03 ml of an acetonitrile solution (0.1 mol / L) of methyl salicylate (MSA), which is released when plants are infected with pathogenic bacteria, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence emission (Figure 11(b)). The results showed that TbC does not emit fluorescence on its own, but reacts with methyl salicylate to emit fluorescence, demonstrating its ability to sense methyl salicylate.

[0062] (Comparative Example 5) 0.05 g of terbium(III) chloride hexahydrate (TbC) was dissolved in 2 mL of water, and 0.2 mL of this solution was dropped onto a circular filter paper (45 mm diameter) and allowed to dry, yielding TbC-containing filter paper. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence (Figure 12(a)). Next, 0.03 mL of an acetonitrile solution (0.1 mol / L) of methyl jasmonate, a signal substance released by plants when they are damaged by pests, was dropped onto the filter paper and allowed to dry. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence (Figure 12(b)). The results indicated that TbC did not react with methyl jasmonate and did not emit fluorescence (Figure 12(b)).

[0063] The results of Example 7 and Comparative Example 5 demonstrate that TbC can selectively sense methyl salicylate, which is released by plants when infected with pathogenic bacteria.

[0064] (Synthesis Example 1) [Terbium acetate and triphenylphosphine oxide complex (TbA-TPO)] 0.3 g of terbium acetate tetrahydrate and 0.409 g of triphenylphosphine oxide were dissolved in 15 ml of methanol and heated under reflux for 4 hours. After cooling, the precipitated crystals were filtered off to obtain 0.177 g of the target terbium acetate and triphenylphosphine oxide complex.

[0065] [ka]

[0066] (Synthesis Example 2) [Terbium acetate and tris(4-methoxyphenyl)phosphine oxide complex (TbA-MTPO)] 0.3 g of terbium acetate tetrahydrate and 0.665 g of tris(4-methoxyphenyl)phosphine oxide were dissolved in 15 ml of methanol and heated under reflux for 4 hours. After cooling, the precipitated crystals were filtered off to obtain 0.118 g of the target terbium acetate and tris(4-methoxyphenyl)phosphine oxide complex.

[0067] [ka]

[0068] Example 8 A 0.2 ml solution of 0.01 g of terbium acetate and triphenylphosphine oxide complex (TbA-TPO) dissolved in 1 ml of DMSO was dropped onto a circular filter paper (45 mm diameter) and dried to obtain filter paper containing TbA-TPO. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence (Figure 13(a)). Next, an acetonitrile solution of methyl salicylate (MSA), which is released when plants are infected with pathogenic bacteria, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence (Figure 13(b)). The results showed that TbA-TPO does not emit fluorescence on its own, but reacts with methyl salicylate to emit fluorescence, demonstrating its ability to sense methyl salicylate.

[0069] In addition, an acetonitrile solution of methyl jasmonate (MJA), a signal substance released by plants when they are damaged by pests, was dropped onto filter paper containing TbA-TPO (Figure 13(c)), and then dried. The resulting filter paper was similarly excited with a UV lamp to confirm whether fluorescence was present (Figure 13(d)). As a result, TbA-TPO did not react with methyl jasmonate and did not emit fluorescence, indicating that TbA-TPO can selectively sense methyl salicylate, which is released by plants when infected with pathogenic fungi.

[0070] Example 9 A 0.2 ml solution of 0.01 g of terbium acetate and tris(4-methoxytriphenyl)phosphine oxide complex (TbA-MTPO) dissolved in 1 ml of DMSO was dropped onto a circular filter paper (45 mm diameter) and dried to obtain TbA-MTPO-containing filter paper. The resulting filter paper was excited with a UV lamp (wavelength 365 nm) to confirm fluorescence (Figure 14(a)). Next, an acetonitrile solution of methyl salicylate (MSA), which is released when plants are infected with pathogenic fungi, was dropped onto the filter paper and dried. The resulting filter paper was similarly excited with a UV lamp to confirm fluorescence (Figure 14(b)). The results showed that TbA-MTPO does not emit fluorescence on its own, but it reacts with methyl salicylate to emit fluorescence, demonstrating its ability to sense methyl salicylate.

[0071] In addition, an acetonitrile solution of methyl jasmonate (MJA), a signal substance released by plants when they are damaged by pests, was dropped onto filter paper containing TbA-MTPO (Figure 14(c)), and then dried. The resulting filter paper was similarly excited with a UV lamp to confirm whether fluorescence was present (Figure 14(d)). As a result, TbA-MTPO did not react with methyl jasmonate and did not emit fluorescence, indicating that TbA-MTPO can selectively sense methyl salicylate, which plants release when infected with pathogenic bacteria.

[0072] Example 10 [Fluorescence spectrum measurement] 0.9 ml of a DMSO solution (0.0015 mol / L) of terbium acetate tetrahydrate (TbA) and triphenylphosphine oxide complex (TbA-TPO) was mixed with 0.1 ml of a DMSO solution (0.0015 mol / L). After 10 minutes, the solution was diluted 20-fold and placed in a quartz cell. The fluorescence spectrum was measured at an excitation wavelength of 365 nm. Similarly, 0.9 ml of a DMSO solution (0.0015 mol / L) of TbA-TPO was mixed with 0.1 ml of DMSO, further diluted 20-fold, and placed in a quartz cell. The fluorescence spectrum was measured at an excitation wavelength of 365 nm. Similarly, 0.1 ml of a DMSO solution (0.0015 mol / L) of MSA was mixed with 0.9 ml of DMSO, further diluted 20-fold, and placed in a quartz cell. The fluorescence spectrum was measured at an excitation wavelength of 365 nm. The obtained fluorescence spectrum curves are shown in Figure 15. The solid line represents the fluorescence spectrum of TbA-TPO+MSA, the dashed line represents the fluorescence spectrum of TbA-TPO alone, and the dashed line represents the fluorescence spectrum of MSA alone.

[0073] These results show that TbA-TPO does not exhibit fluorescence by itself, but emits fluorescence (maximum wavelength 546 nm) when it reacts with MSA. Furthermore, MSA alone does not emit fluorescence in the range of 480 to 630 nm, but it emits fluorescence when TbA-TPO reacts with methyl salicylate.

[0074] Example 11 [Detection of MSA using agarose gel containing rare earth salts] 0.125 g of terbium acetate tetrahydrate (TbA) and 1 g of agarose were dispersed in 49 g of water, and the agarose was dissolved and converted into a sol by heating and stirring at 95°C. The mixture was then allowed to cool, yielding a gel containing TbA. A portion of the resulting gel was taken and excited with a UV lamp (wavelength 365 nm) to check for fluorescence, but no fluorescence was observed (Figure 16(a)).

[0075] Next, this gel and 10 mg of methyl salicylate were placed in a petri dish and stored in a desiccator without direct contact. After 6 hours, the gel was removed and excited with a UV lamp (wavelength 365 nm) to evaluate whether fluorescence was present. Yellow-green fluorescence was confirmed (Figure 16(b)). This result demonstrated that the TbA-containing gel can sense methyl salicylate, which is released by plants when infected with pathogens, as a volatile signal.

[0076] Example 12 [Detection of MSA at a concentration of 13 ppm] 0.2 ml of a solution of 0.1 g of terbium acetate tetrahydrate (TbA) dissolved in 2 ml of water was dropped onto a circular filter paper (45 mm diameter) and dried to obtain a filter paper containing TbA. The resulting filter paper was placed in an 800 ml desiccator adjusted to an MSA concentration of 13 ppm. After 3 hours, the filter paper was removed and fluorescence emission was confirmed at an excitation wavelength of 365 nm. The results are shown in Figure 17. The unexposed sample (left) did not exhibit the yellow-green fluorescence characteristic of Tb complexes, but after 3 hours of exposure (right), yellow-green fluorescence emission was confirmed. These results demonstrate that TbA can sense MSA at the 10 ppm level.

[0077] Example 13 [Quantitative evaluation of fluorescence intensity] 0.5 ml of a DMSO solution of TbA (concentration 0.0005 mol / L) and 0.5 ml of a DMSO solution of MSA (concentration 0.0005 mol / L) were added, and after 10 minutes, the solution was diluted 40-fold and placed in a quartz cell. The fluorescence spectrum was measured at an excitation wavelength of 365 nm, resulting in the fluorescence spectrum curve shown in Figure 18. The peak wavelength at which the fluorescence intensity was strongest was 547 nm, indicating that the fluorescence emission wavelength is characteristic of terbium complexes. Next, 0.9 ml of a DMSO solution of TbA (concentration 0.0005 mol / L) and 0.1 ml of a DMSO solution of MSA (concentration 0.0005 mol / L) were added, and after 10 minutes, the solution was diluted 40-fold and the fluorescence spectrum was measured at an excitation wavelength of 365 nm. The fluorescence intensity at a wavelength of 547 nm was determined.

[0078] Similarly, the fluorescence intensity was measured for 0.8 ml of TbA solution and 0.2 ml of MSA solution, and for 0.7 ml of TbA solution and 0.3 ml of MSA solution. The obtained fluorescence intensities are plotted in Figure 19. From these results, it was found that the fluorescence intensity increased as the proportion of MSA increased, and that MSA could be quantitatively detected.

[0079] Example 14 [Measurement of electrochemical behavior] Tetrabutylammonium perchlorate was dissolved in DMSO as a supporting electrolyte to prepare an electrolyte solution (concentration: 0.1 mol / L). 10 ml of the electrolyte solution was placed in a glass container to form a three-electrode electrochemical cell consisting of a working electrode, a counter electrode, and a reference electrode. The working electrode was glassy carbon, the counter electrode was Pt, and the reference electrode was Ag / Ag. + 0.1 ml of a DMSO solution of TbA (concentration: 0.1 mol / L) was added to the electrode, and cyclic voltammetry (CV) was measured at room temperature (sweep potential: -0.8 to 1.2 V, sweep rate: 0.1 V / s).

[0080] Next, 0.1 ml of a DMSO solution of methyl salicylate (MSA) (concentration: 0.1 mol / L) was added thereto, and CV measurement was carried out in the same manner.

[0081] The obtained current-voltage curves (cyclic voltammograms) are shown in Figure 20. The dashed line shows the measurement results for TbA only, and the solid line shows the measurement results after adding MSA to TbA. From these results, it was found that after adding MSA, new reduction peaks appeared at potentials of -0.08 V and -0.46 V compared to before addition. This indicates that, for example, at the voltage (Ag / Ag) where the current value changes significantly before and after the reaction with MSA, + By monitoring the current flowing through the electrode at potentials of -0.08V and -0.46V relative to the electrode, it was demonstrated that the plant hormone methyl salicylate could be sensed by changes in the current value.

[0082] (Synthesis Example 3) [Terbium pivalate] 1 g of terbium chloride hexahydrate was dissolved in 20 ml of water, and 1.142 g of sodium pivalate dissolved in 20 ml of water was added to the solution, followed by stirring at room temperature for 1 hour. The precipitated crystals were filtered off and washed with water to obtain 0.742 g of terbium pivalate as a white powder.

[0083] Example 15 [Fluorescence detection of methyl salicylate using terbium pivalate] 0.9 ml of a DMSO solution of terbium pivalate (TbPv) (0.0015 mol / L) and 0.1 ml of a DMSO solution of methyl salicylate (MSA) (0.0015 mol / L) were mixed and, after 10 minutes, diluted 20-fold. The resulting solution was placed in a quartz cell and the fluorescence spectrum was measured at an excitation wavelength of 365 nm. Also, 0.9 ml of a DMSO solution of TbPv (0.0015 mol / L) was mixed with 0.1 ml of DMSO and further diluted 20-fold. The resulting solution was placed in a quartz cell and the fluorescence spectrum was measured at an excitation wavelength of 365 nm. The resulting fluorescence spectrum is shown in Figure 21. The solid line represents the fluorescence spectrum of TbPv + MSA, and the dashed line represents the fluorescence spectrum of TbPv alone. These results demonstrate that TbPv does not exhibit fluorescence by itself, but exhibits fluorescence emission (maximum wavelength 546 nm) upon reacting with MSA.

[0084] Some or all of the above embodiments can be described as in the following supplementary notes, but the disclosure of the present application is not limited to the following supplementary notes. (Appendix 1) A method for sensing methyl salicylate, which uses a rare earth compound as a receptor that selectively recognizes methyl salicylate. (Appendix 2) 2. The sensing method of claim 1, wherein the rare earth compound is any one of acetate, chloride, oxalate, nitrate, propionate, isobutyrate, and pivalate of scandium (Sc), yttrium (Y), lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu). (Appendix 3) A sensing method as described in Appendix 1, wherein the rare earth compound is any one of acetate, chloride, oxalate, nitrate, propionate, isobutyrate, and pivalate of samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), and dysprosium (Dy). (Appendix 4) 2. The sensing method according to claim 1, wherein the rare earth compound is a compound that forms a complex with a phosphine oxide derivative. (Appendix 5) 5. The sensing method according to any one of claims 1 to 4, which utilizes a phenomenon in which methyl salicylate reacts with a rare earth compound to form a rare earth complex, thereby emitting fluorescence. (Appendix 6) 6. The sensing method according to any one of claims 1 to 5, which utilizes a phenomenon in which electrochemical behavior changes due to a reaction between a rare earth compound and methyl salicylate. (Appendix 7) 7. A sensing method according to claim 6, which utilizes a change in current value caused by a reaction between a rare earth compound and methyl salicylate. (Appendix 8) A methyl salicylate sensor for detecting methyl salicylate, comprising at least i) a recognition unit for methyl salicylate having a rare earth compound, and ii) a detection unit for detecting that methyl salicylate has been recognized by the recognition unit. (Appendix 9) A method for detecting pathogenic fungal infection of agricultural crops, comprising placing the methyl salicylate sensor according to Appendix 8 near the crops and detecting methyl salicylate with the sensor. (Appendix 10) A methyl salicylate sensor for detecting methyl salicylate, comprising at least a methyl salicylate recognition unit having a rare earth compound as a receptor that selectively recognizes methyl salicylate, and a detection unit that detects the recognition of methyl salicylate by the recognition unit, wherein the detection unit includes an optical and / or electrochemical detection element and a computer, and the computer has a program that causes it to execute the following steps: i) receiving a signal from the optical and / or electrochemical detection element; ii) analyzing the received signal to determine the presence or absence and / or concentration of methyl salicylate; and iii) outputting the analysis results. (Appendix 11) A program for controlling a methyl salicylate sensor for detecting methyl salicylate, the methyl salicylate sensor comprising at least a recognition unit for methyl salicylate having a rare earth compound as a receptor that selectively recognizes methyl salicylate, and a detection unit that detects the recognition of methyl salicylate by the recognition unit, the detection unit including an optical and / or electrochemical detection element and a computer, the program causing the computer to execute the steps of: i) receiving a signal from the optical and / or electrochemical detection element; ii) analyzing the received signal to determine the presence or absence and / or concentration of methyl salicylate; and iii) outputting the analysis results. (Appendix 12) A method for detecting methyl salicylate, comprising the steps of: (i) reacting a rare earth compound with methyl salicylate to form a complex; (ii) irradiating the complex with excitation light; and (iii) detecting the fluorescence emitted by the complex. (Appendix 13) 13. The detection method according to claim 12, wherein a wavelength in the range of 200 to 400 nm is used as the excitation wavelength. (Appendix 14) 14. The detection method of claim 12 or 13, further comprising determining the concentration of methyl salicylate by comparing the intensity of the detected fluorescence with a predetermined reference value. (Appendix 15) A method for detecting methyl salicylate, comprising the steps of: (i) reacting a rare earth compound with methyl salicylate in a solution to form a complex; (ii) measuring the current flowing through the solution under a constant voltage; and (iii) detecting a change in the current value resulting from the formation of the complex. (Appendix 16) 16. The detection method according to claim 15, wherein the voltage value is within the range of −1 to 2 V. (Appendix 17) 17. The detection method according to claim 15 or 16, wherein the solution contains tetrabutylammonium perchlorate as a supporting electrolyte. (Appendix 18) 18. The detection method according to any one of claims 15 to 17, further comprising the step of determining the concentration of methyl salicylate by comparing the detected change in current value with a predetermined reference value. (Appendix 19) 19. The detection method according to any one of claims 12 to 18, wherein the rare earth compound is selected from the group consisting of terbium(III) acetate tetrahydrate, gadolinium(III) acetate tetrahydrate, samarium(III) acetate hydrate, dysprosium(III) acetate tetrahydrate, terbium pivalate, and terbium(III) chloride hexahydrate. (Appendix 20) A methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for optically detecting that methyl salicylate has been recognized by the recognition unit. (Appendix 21) 21. The methyl salicylate sensor according to claim 20, wherein the optical detection unit includes at least an excitation light source and a detection element. (Appendix 22) A methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for electrochemically detecting that methyl salicylate has been recognized by the recognition unit. (Appendix 23) 23. The methyl salicylate sensor according to claim 22, wherein the electrochemical detection unit comprises an electrochemical cell having electrodes for detecting a current generated by oxidation of a complex formed between the rare earth compound and methyl salicylate. (Appendix 24) A method for detecting pathogenic fungal infection of agricultural crops, comprising placing the methyl salicylate sensor according to claim 10 in the vicinity of the crops and detecting methyl salicylate with the sensor. (Appendix 25) A method for detecting pathogen infection of agricultural crops according to Appendix 9 or Appendix 24, characterized in that the methyl salicylate sensor according to Appendix 10 is placed within 2 m of the agricultural crops.

[0085] This application claims priority based on Japanese Patent Application No. 2020-96909, filed on June 3, 2020, and Japanese Patent Application No. 2021-39138, filed on March 11, 2021, the disclosures of which are incorporated herein in their entireties.

[0086] Although the present invention has been described above with reference to the embodiments and examples, the present invention is not limited to the above-described embodiments and examples. Various modifications that can be understood by those skilled in the art can be made to the configuration and details of the present invention within the scope of the present invention. [Industrial Applicability]

[0087] Sensing using a rare earth compound according to an embodiment of the present invention as a receptor for detecting the plant hormone methyl salicylate selectively forms a complex with methyl salicylate and exhibits a fluorescence emission phenomenon and changes in electrochemical behavior, making it possible to selectively detect methyl salicylate, a plant hormone released by plants when infected with pathogenic bacteria. Furthermore, by using a sensor that uses rare earth compounds as a recognition element, it is possible to detect disease infection in plants at an early stage. Specifically, this sensor can be used as a new sensor for agricultural ICT in greenhouses and other horticulture facilities, as it can detect disease infection in agricultural crops at an early stage.

Claims

1. A program for controlling a methyl salicylate sensor having a recognition unit for methyl salicylate, which has a rare earth compound as a receptor for recognizing methyl salicylate, and an optical and / or electrochemical detection element for detecting the recognition of methyl salicylate by said recognition unit, said program comprising: i) means for receiving signals from the optical and / or electrochemical sensing element; ii) means for analyzing the received signal to determine the presence and / or concentration of methyl salicylate; and iii) A program that functions as a means for outputting the analysis results.

2. A method for detecting methyl salicylate, comprising the steps of: (i) reacting a rare earth compound with methyl salicylate to form a complex; (ii) irradiating the complex with excitation light; and (iii) detecting fluorescence emitted by the complex.

3. 3. The detection method according to claim 2, wherein a wavelength in the range of 200 to 400 nm is used as the excitation wavelength.

4. 4. The method of claim 2, further comprising the step of determining the concentration of methyl salicylate by comparing the intensity of the detected fluorescence with a predetermined reference value.

5. (i) reacting a rare earth compound with methyl salicylate in a solution to form a complex; A method for detecting methyl salicylate, comprising: (ii) measuring the current flowing through the solution under a constant voltage; and (iii) detecting a change in the current value resulting from the formation of a complex.

6. 6. The detection method according to claim 5, wherein the voltage value is within the range of −1 to 2 V.

7. A methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for optically detecting that methyl salicylate has been recognized by the recognition unit.

8. 8. The methyl salicylate sensor according to claim 7, wherein the detection unit includes at least an excitation light source and a detection element.

9. A methyl salicylate sensor for detecting methyl salicylate, comprising at least (i) a recognition unit for methyl salicylate having a rare earth compound, and (ii) a detection unit for electrochemically detecting that methyl salicylate has been recognized by the recognition unit.

10. A method for detecting pathogen infection of agricultural crops, comprising placing the methyl salicylate sensor according to any one of claims 7 to 9 in the vicinity of the crops and detecting methyl salicylate with the sensor.

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