The present invention relates to a microorganism culture kit and related methods of culturing microorganisms using such devices.
It has been said that only about 1% of microorganisms in the environment can be cultured by a conventionally performed agar-plate surface smear method. Such methods are limited due to several constraints. First, due to the closed culture environment, it is not possible to easily remove substances generated by the cultured microorganism. As a result, metabolites of the microorganism and environmental components accumulate in the culture and inhibit the growth and multiplication of the microorganism. Furthermore, it is difficult to maintain in a solid medium the concentration of a nutrient required for the growth of a target microorganism.
Prior researchers have attempted to addresses these concerns by performing the culturing while a liquid medium is continuously supplied, or by culturing microorganisms on a solid medium placed in a natural environment. Examples of such methods are described in Japanese Patent Application Pub. No. 2016-86654 and in U.S. Pat. No. 7,011,957, the entire contents of each of which being incorporated herein by reference. However, these methods are fail to provide an effective solution (e.g., due to the instability associated with attempts to culture microorganisms in a natural environment and limitations on the parameters that can be modified).
In some aspects, the present disclosure provides a microorganism culture kit that can be used to provide various culture conditions. These devices implement a simple design that can be rapidly configured, allowing researchers to study otherwise difficult to culture microorganisms. In some aspects, a microorganism culture kit according to the present invention includes: two frame bodies, in which the two frame bodies are each a first-type frame body or are the first-type frame body and a second-type frame body, in which the first-type frame body includes a first frame body surrounding a first internal space, the first frame body including an inflow passage for a fluid to flow into the first internal space and an outflow passage for the fluid to flow out from the first internal space, the inflow passage and the outflow passage being each provided to be openable and closable, in which the second-type frame body includes a second frame body surrounding a second internal space, and in which the two frame bodies are stackable on each other.
In some aspects, the first-type frame body is configured, in a state in which the inflow passage and the outflow passage are open, to circulate a nutrient-containing gas, a nutrient-containing liquid, an environmental component-containing gas, or an environmental component-containing liquid in the first internal space and able, in a state in which the inflow passage and the outflow passage are closed, to hold a microorganism-containing medium, a nutrient-containing material, or an environmental component-containing material in the first internal space, and wherein the second-type frame body is configured to hold a microorganism-containing medium, a nutrient-containing material, or an environmental component-containing material in the second internal space.
In some aspects, each of the two frame bodies has an annular shape and has an internal thread and an external thread, the two frame bodies being configured to be stacked on and coupled to each other as a result of the internal thread of one of the frame bodies being screwed with the external thread of the other of the frame bodies.
In some aspects, the two frame bodies are each a first-type frame body.
In some aspects, the two frame bodies are each a second-type frame body.
In some aspects, the first-type frame body includes a pipe extending outward from the inflow passage, wherein the pipe is configured to allow a fluid to be added to and flow into the inflow passage
In some aspects, the microorganism culture kit comprises a cap body configured to close the first internal space and/or the second internal space of the frame bodies that are stacked on each other to cover the first internal space and/or the second internal space, and/or a base that supports the frame bodies that are stacked on each other
In some aspects, the first-type frame body includes a pipe extending outward from the outflow passage, wherein the pipe is configured to allow a fluid to flow into the outflow passage.
In some aspects, the microorganism culture kit comprises a cap body configured to close the first internal space and the second internal space of the frame bodies that are stacked on each other to cover the first internal space and the second internal space.
In another general aspect, the disclosure provides methods of culturing a microorganism. For example, in some aspects, a method of culturing a microorganism, comprising: providing a microorganism-containing medium; and placing the microorganism-containing medium in any of the microorganism culture kits described herein. In some aspects, the microorganism-containing medium is placed in the first-type frame body or the second-type frame body of the microorganism culture kit. In some aspects, the microorganism-containing medium is placed in the first internal space of the first-type frame body or the second internal space of the first-type frame body.
Aspects of the present disclosure will be more specifically described below, with reference to the drawings where appropriate. However, it should be understood that while exemplary devices and methods are described, the present disclosure is not necessarily limited to those devices and methods alone.
In some aspects, a microorganism culture kit according to the present embodiment includes two frame bodies stackable on each other. As illustrated in
As illustrated in
Further, the first frame body 12 may an inflow passage 13 for a fluid to flow into the internal space 11 and an outflow passage 14 for the fluid to flow out from the internal space 11. In some aspects, it is preferable that a pipe 15 and/or a pipe 16, such as those illustrated in
In a state in which the inflow passage 13 and the outflow passage 14 are open, the first-type frame body 1 is capable of circulating a fluid in the first internal space 11. The fluid is a nutrient-containing gas, a nutrient-containing liquid, an environmental component-containing gas, or an environmental component-containing liquid. In a state in which the inflow passage 13 and the outflow passage 14 are closed, the first-type frame body 1 is capable of holding, in the first internal space 11, a microorganism-containing medium, a nutrient-containing material, or an environmental component-containing material.
The microorganism culture kit 10A according to the present embodiment may be used as follows. As illustrated in
In some aspects, preferably, the first-type frame body 1 at the lower layer is stacked on a base 8. The base 8 is illustrated in
In some aspects, preferably, the first-type frame body 1 at the upper layer is closed by a cap body 7 to cover the first internal space 11. The cap body 7 is illustrated in
A microorganism culture apparatus 100A, having the aforementioned configuration, allows for the circulation of a nutrient-containing liquid in the first internal space 11 of the first-type frame body 1 at the upper layer to supply a nutrient from the upper side to a microorganism in the first internal space 11 of the first-type frame body 1 at the lower layer, and it is thus possible to culture the microorganism.
In some aspects, instead of a nutrient-containing liquid, a nutrient-containing gas, an environmental component-containing gas, or an environmental component-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the upper layer. When an environmental component-containing gas or an environmental component-containing liquid is circulated, it is possible to supply an environmental component from the upper side to a microorganism in the first internal space 11 of the first-type frame body 1 at the lower layer, and it is thus possible to culture the microorganism.
Thus, when using microorganism culture apparatus 100A, one may culture a microorganism with minimal difficulty, and, moreover, it is possible to easily change the type, the concentration, and the like of a nutrient or an environmental component that is to be supplied. Therefore, it is possible to implement various culture conditions and to study various microorganisms that are difficult to be cultured using traditional methods.
A microorganism culture kit 10A according to the present embodiment can provide various benefits. The microorganism culture apparatus 100A having a two-layer stack structure, such as that illustrated in
As illustrated in
In some aspects, preferably, one of the first-type frame bodies 1 is provided with one or more types of sensors that detect a culture state. The sensors may be selected from a temperature sensor, a pH sensor, and a gas concentration sensor. In some aspects, preferably, one or more types of stimulation apply portions that apply physical stimulation to a microorganism-containing medium from outside is attached to the same one of the first-type frame bodies 1. One of the first-type frame bodies may be used to hold a microorganism-containing medium.
For example, in the microorganism culture apparatus 100A illustrated in
In some aspects, both of the two first-type frame bodies 1 may be used in a state in which the inflow passage 13 and the outflow passage 14 are closed. For example, in the microorganism culture apparatus 100A illustrated in
In some aspects, the microorganism culture kit according to the present embodiment includes two frame bodies stackable on each other. As illustrated in
The first-type frame body 1 is the same as the first-type frame body 1 according to the first embodiment. The external fitting portion 122 of the first-type frame body 1 has dimensions that enable external fitting to the internal fitting portion 224 of the second-type frame body 2, and the internal fitting portion 124 of the first-type frame body 1 has dimensions that enable internal fitting to the external fitting portion 222 of the second-type frame body 2.
As illustrated in, for example,
The second-type frame body 2 may be capable of holding, in the second internal space 21, a microorganism-containing medium, a nutrient-containing material, or an environmental component-containing material.
A microorganism culture kit 10B according to the present embodiment provides several benefits. As illustrated in
In some aspects, the second-type frame body 2 at the lower layer is stacked on the base 8. In some aspects, preferably, the first-type frame body 1 at the upper layer is closed by the cap body 7. The cap body 7 and the base 8 are the same as the cap body 7 and the base 8 used in the first embodiment. The external fitting portion 72 of the cap body 7 has dimensions that enable external fitting to the internal fitting portion 224 of the second-type frame body 2, and the internal fitting portion 82 of the base 8 has dimensions that enable internal fitting to the external fitting portion 222 of the second-type frame body 2.
A microorganism culture apparatus 100B, having the aforementioned configuration, is able to circulate a nutrient-containing liquid in the first internal space 11 of the first-type frame body 1 at the upper layer to supply a nutrient from the upper side to a microorganism in the second internal space 21 of the second-type frame body 2 at the lower layer, and it is thus possible to culture the microorganism.
Instead of a nutrient-containing liquid, a nutrient-containing gas, an environmental component-containing gas, or an environmental component-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the upper layer. When an environmental component-containing gas or an environmental component-containing liquid is circulated, it is possible to supply an environmental component from the upper side to a microorganism in the second internal space 21 of the second-type frame body 2 at the lower layer, and it is thus possible to culture the microorganism.
Thus, according to the microorganism culture apparatus 100B, it is possible to culture a microorganism with minimal difficulty, and, moreover, it is possible to easily change the type, the concentration, and the like of a nutrient or an environmental component that is to be supplied. Therefore, it is possible to replicate various culture conditions and study various microorganisms that are difficult to be cultured using traditional methods.
The microorganism culture kit 10B according to the present embodiment can provide various benefits. The microorganism culture apparatus 100B having a two-layer stack structure, such as that illustrated in
As illustrated in
In some aspects, the second-type frame body 2 is provided with one or more types of sensors configured to detect a culture state. The sensors may be selected from a temperature sensor, a pH sensor, and a gas concentration sensor. In some aspects, the sensors may be configured to monitor or detect the state of a microorganism-containing medium and are attached to the second-type frame body 2. The second-type frame body 2 may be used to hold the microorganism-containing medium. For example, in the microorganism culture apparatus 100B illustrated in
As illustrated in
A microorganism culture kit according to the present embodiment further includes one frame body additionally in the microorganism culture kit 10A according to the first embodiment. The additional one frame body is the first-type frame body 1 or the second-type frame body 2. That is, the microorganism culture kit according to the present embodiment includes a microorganism culture kit 10C including, as illustrated in
The microorganism culture kit 10C according to the present embodiment may be used as follows. As illustrated in
The three first-type frame bodies 1 may be stacked on and coupled to each other as a result of the internal thread 121 of the first-type frame body 1 positioned at an upper location being screwed with the external thread 123 of the first-type frame body 1 positioned at a lower location. The first-type frame bodies 1 coupled to each other are sealed by the O-ring 125.
In some aspects, preferably, the first-type frame body 1 at the lower layer is stacked on the base 8. Preferably, the first-type frame body 1 at the upper layer is closed by the cap body 7. The cap body 7 and the base 8 are the same as the cap body 7 and the base 8 used in the first embodiment and the second embodiment.
A microorganism culture apparatus 100C having the aforementioned configuration allows for the circulation of a nutrient-containing liquid in the first internal space 11 of the first-type frame body 1 at the upper layer and circulating an environmental component-containing liquid in the first internal space 11 of the first-type frame body 1 at the lower layer to supply a nutrient from the upper side and an environmental component from the lower side to a microorganism in the first internal space 11 of the first-type frame body 1 at the intermediate layer, and it is thus possible to culture the microorganism.
Instead of a nutrient-containing liquid, a nutrient-containing gas, an environmental component-containing gas, or an environmental component-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the upper layer. When an environmental component-containing gas or an environmental component-containing liquid is circulated, it is possible to supply an environmental component also from the upper side to a microorganism in the first internal space 11 of the first-type frame body 1 at the intermediate layer, and it is thus possible to culture the microorganism.
Instead of an environmental component-containing liquid, an environmental component-containing gas, a nutrient-containing gas, or a nutrient-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the lower layer. When a nutrient-containing gas or a nutrient-containing liquid is circulated, it is possible to supply a nutrient also from the lower side to a microorganism in the first internal space 11 of the first-type frame body 1 at the intermediate layer, and it is thus possible to culture the microorganism.
The microorganism culture kit 10C according to the present embodiment provides several benefits. The microorganism culture apparatus 100C having a three-layer stack structure, such as that illustrated in
In the microorganism culture apparatus 100C, not only the first-type frame body 1 disposed at the intermediate layer but also the first-type frame body 1 disposed at at least one of the upper layer and the lower layer may be used in a state in which the inflow passage 13 and the outflow passage 14 are closed. In the microorganism culture apparatus 100C illustrated in
The microorganism culture kit 10D according to the present embodiment is usable as follows. As illustrated by
The first-type frame body 1 and the second-type frame body 2 can be stacked on and coupled to each other as a result of the internal thread 121 of the first-type frame body 1 positioned at an upper location being screwed with the external thread 223 of the second-type frame body 2 positioned at a lower location, the first-type frame body 1 and the second-type frame body 2 being sealed by the O-ring 225, and the second-type frame body 2 and the first-type frame body 1 can be stacked on and coupled to each other as a result of the internal thread 221 of the second-type frame body 2 positioned at an upper location being screwed with the external thread 123 of the first-type frame body 1 positioned at a lower location, the second-type frame body 2 and the first-type frame body 1 being sealed by the O-ring 125.
In some aspects, preferably, the first-type frame body 1 at the lower layer is stacked on the base 8. The the first-type frame body 1 at the upper layer may be closed by the cap body 7. The cap body 7 and the base 8 are the same as the cap body 7 and the base 8 used in the first embodiment and the second embodiment.
A microorganism culture apparatus 100D having the aforementioned configuration it capable of circulating a nutrient-containing liquid in the first internal space 11 of the first-type frame body 1 at the upper layer and circulating an environmental component-containing liquid in the first internal space 11 of the first-type frame body 1 at the lower layer to supply a nutrient from the upper side and supply an environmental component from the lower side to a microorganism in the second internal space 21 of the second-type frame body 2 at the intermediate layer, and it is thus possible to culture the microorganism.
Instead of a nutrient-containing liquid, a nutrient-containing gas, an environmental component-containing gas, or an environmental component-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the upper layer. When an environmental component-containing gas or an environmental component-containing liquid is circulated, it is possible to supply an environmental component also from the upper side to a microorganism in the second internal space 21 of the second-type frame body 2 at the intermediate layer, and it is thus possible to culture the microorganism.
Instead of an environmental component-containing liquid, an environmental component-containing gas, a nutrient-containing gas, or a nutrient-containing liquid may be circulated in the first internal space 11 of the first-type frame body 1 at the lower layer. When a nutrient-containing gas or a nutrient-containing liquid is circulated, it is possible to supply a nutrient also from the lower side to a microorganism in the second internal space 21 of the second-type frame body 2 at the intermediate layer, and it is thus possible to culture the microorganism.
The microorganism culture kit 10D according to the present embodiment can exert the following effects. (a) The microorganism culture apparatus 100D having a three-layer stack structure, such as that illustrated in
In the microorganism culture apparatus 100D, the first-type frame body 1 disposed at at least one of the upper layer and the lower layer may be used in a state in which the inflow passage 13 and the outflow passage 14 are closed. In the microorganism culture apparatus 100D illustrated in
In some aspects, a microorganism culture kit according to the present embodiment further includes one frame body additionally in the microorganism culture kit 10B according to the second embodiment. The additional one frame body may be the first-type frame body 1. That is, the microorganism culture kit according to the present embodiment includes two first-type frame bodies 1 and one second-type frame body 2. Therefore, a microorganism culture kit according to the present embodiment is the same as the microorganism culture kit 10D according to the third embodiment.
In some aspects, a microorganism culture kit according to the present embodiment includes a plurality of microorganism culture kits selected optionally from the microorganism culture kits 10A to 10D according to the first embodiment to the fourth embodiment. Thus, it is possible to configure a multilayer stack structure body by stacking four or more frame bodies on each other, and the multilayer stack structure body is usable as a microorganism culture apparatus.
In the seven-layer stack structure body, the lowermost layer (the first layer) may be the first-type frame body 1, the second layer to the sixth layer may be the second-type frame bodies 2, and the uppermost layer (the seventh layer) may be the first-type frame body 1. The first-type frame body 1 at the first layer may be stacked on the base 8, and the first-type frame body 1 at the seventh layer may be closed by the cap body 7.
A microorganism culture apparatus 100E is configured such that the first-type frame body 1 at the first layer circulates an environmental component-containing liquid or an environmental component-containing gas, the second-type frame bodies 2 at the second layer to the fourth layer each hold a microorganism-containing medium, the second-type frame body 2 at the fifth layer holds a nutrient-containing material, and the first-type frame body 1 at the seventh layer circulates a nutrient-containing liquid or a nutrient-containing gas.
That is, as illustrated in
A microorganism culture apparatus 100E provides several benefits. First, it is capable of circulating an environmental component-containing liquid or an environmental component-containing gas in the first-type frame body 1 at the first layer to supply an environmental component from the lower side and supply a nutrient from the upper side to a microorganisms in each of the second-type frame bodies 2 at the second layer to the fourth layer, and it is thus possible to culture the microorganisms in the second-type frame bodies 2 at the second layer to the fourth layer. It is also capable of circulating a nutrient-containing liquid or a nutrient-containing gas in the first-type frame body 1 at the seventh layer to supply a nutrient from the lower side and the upper side to a microorganism in the second-type frame body 2 at the sixth layer, and it is thus possible to culture the microorganism in the second-type frame body 2 at the sixth layer. In some aspects, it is possible to achieve two types of culture conditions due to culture conditions in the stack structure body of the first layer to the fifth layer and culture conditions in the stack structure body of the fifth layer to the seventh layer differ from each other. Therefore, it is possible to improve work efficiency in selection of culture conditions, and it is thus possible to increase the possibility of acquisition of a microorganism that is difficult to be cultured. In the second layer to the fourth layer, the culture portion A has a three-layer structure, and thus, the culture conditions in the layers differ from each other. For example, the concentration of a supplied environmental component is highest in the second layer and lowest in the fourth layer. The concentration of a supplied nutrient is highest in the fourth layer and lowest in the second layer. Therefore, it is possible to improve work efficiency in selection of culture conditions, and it is thus possible to increase the possibility of acquisition of a microorganism that is difficult to be cultured.
It is possible to culture a microorganism only by circulating an environmental component-containing liquid or an environmental component-containing gas in the first layer and circulating a nutrient-containing liquid or a nutrient-containing gas in the seventh layer, and it is thus possible to perform culture of the microorganism easily. Consequently, it is possible to increase the possibility of acquisition of a microorganism that is difficult to be cultured. It is possible to assemble the apparatus by only coupling the first-type frame bodies 1 and the second-type frame bodies 2 to each other, and it is thus possible to improve efficiency in the production of the apparatus.
In some aspects, it is possible to detach the first-type frame bodies 1 and the second-type frame bodies 2 easily by only releasing the coupling and possible to newly couple another first-type frame body 1 or second-type frame body 2 instead. That is, each layer is easily replaceable. Therefore, it is possible to change culture conditions easily and possible to improve work efficiency in selection of culture conditions, and it is thus possible to increase the possibility of acquisition of a microorganism that is difficult to be cultured. For example, the fifth layer and/or the seventh layer that is a nutrient supply portion can be replaced with the first-type frame body 1 or the second-type frame body 2 that is another nutrient supply portion, or can be replaced with the first-type frame body 1 or the second-type frame body 2 that is an environmental component supply portion. In addition, the first layer that is an environmental component supply portion can be replaced with the first-type frame body 1 or the second-type frame body 2 that is another environmental component supply portion or can be replaced with the first-type frame body 1 or the second-type frame body 2 that is a nutrient supply portion.
In some aspects, it is possible to increase the number of layers to increase the number of three-layer stack structure bodies each having the nutrient supply portion B and/or the environmental component supply portion C at both surfaces of the culture portion A. Then, culture conditions can be varied for each of these three-layer stack structure bodies. Therefore, it is possible to improve work efficiency in selection of culture conditions, and it is thus possible to increase the possibility of acquisition of a microorganism that is difficult to be cultured.
In some aspects, it is possible to change at least one of the type and the concentration of a nutrient-containing liquid or a nutrient-containing gas that is circulated in the fifth layer and/or the seventh layer. It is also possible to change at least one of the type and the concentration of an environmental component-containing liquid or an environmental component-containing gas that is circulated in the first layer. Therefore, it is possible to realize various culture conditions easily and possible to easily perform work of selection of culture conditions suitable for a microorganism.
In some aspects, it is possible to detect and monitor culture states of microorganisms in the second layer to the fourth layer and the sixth layer by a temperature sensor 41 and/or a pH sensor 42. Therefore, it is possible to determine culture states in the layers rapidly and appropriately.
On the basis of a result of monitoring, in some aspects it is possible to change at least one of the type and the concentration of a nutrient-containing liquid or a nutrient-containing gas that is circulated in the fifth layer and/or the seventh layer and change at least one of the type and the concentration of an environmental component-containing liquid or an environmental component-containing gas that is circulated in the first layer. Therefore, it is possible to realize culture conditions suitable for a microorganism easily even in the middle of culture. In some aspects, it is possible to activate culture by applying vibrations to microorganisms in the second layer to the fourth layer and the sixth layer by an ultrasonic wave oscillator 43. Therefore, it is possible to improve efficiency in culture.
In addition the exemplary embodiments described above, various other alternative configurations are contemplated. For example, the first-type frame body 1 and the second-type frame body 2 are not limited to have annular shapes and may have outer shapes such as a triangular shape, a quadrangular shape, other polygonal shapes, or an elliptical shape in plan view. Coupling between the first-type frame bodies 1 and coupling between the first-type frame body 1 and the second-type frame body 2 are not limited to be performed by using a screw mechanism that uses an internal thread and an external thread and may be performed by using, for example, a slide fitting mechanism, a recess-projection fitting mechanism or an external coupling member.
In
As illustrated in
The internal space 212 (
When the first-type frame body 1 is used as the culture portion A in a state in which the inflow passage 13 and the outflow passage 14 are closed, the first internal space 11 may be a space that is optionally partitioned in the lateral direction or a space that is optionally partitioned in the up-down direction.
A mechanism that opens and closes the inflow passage 13 and the outflow passage 14 is not limited to a mechanism using the plug 17 and may be a mechanism using an opening-closing cap, a mechanism using a check valve, or the like.
A microorganism culture apparatus 100E configured by using the microorganism culture kit according to the fifth embodiment was tested in this experiment. As illustrated in
Nutrient supply portion (the seventh layer)
Nutrient supply portion (the fifth layer)
The above aqueous agar solution was treated in an autoclave (121° C./20 minutes), 5 mL of a soil-extraction dilute solution was added to the agar aqueous solution when the temperature of the agar aqueous solution reached about 60° C., and after stirred, the agar aqueous solution was packed in the internal space of a jacket as a culture portion. The soil-extraction dilute solution was prepared by stirring 15 mL of pure water after 5 g of soil was added to the pure water, and supernatant obtained after leaving the pure water for one hour was diluted by 10000 times through sequential dilution. A membrane filter VCWP (Merck Millipore Corporation; 0.1 μm) was disposed between portions.
Culturing was performed by circulating the substrate A liquid in the nutrient supply portion (the seventh layer), the substrate B liquid in the nutrient supply portion (the fifth layer), and the soil extraction liquid in the environmental-component supply portion (the first layer) continuously for one week.
After the culture, a colony generated in the culture portion was collected and subjected to a genetic analysis performed by Techno Suruga Laboratory Co., Ltd. Species were identified by performing a homology analysis on about 600 bases in the V1 to V4 regions of 16S rDNA and creating a simple molecular genealogical tree. The percentage of homology indicates the degree of matching between base sequences, and it was determined that a species was new when the percentage of homology was lower than 98%.
DNA extract achromopeptidase (FUJIFILM Wako Chemical Corporation)
PCR amplified PrimeSTAR HS DNA Polymerase (Takara Bio Inc.)
Cycle Sequence BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems)
Base sequence determination ChromasPro 1.7 (Technelysium)
Database DB-BA 12.0 (Techno Suruga Laboratory Co., Ltd.)
For comparison, a colony was generated by an agar-plate surface smear method and subjected to the same genetic analysis as Example #1 above.
1 first-type frame body
11 first internal space
12 first frame body
121 internal thread
123 external thread
13 inflow passage
14 outflow passage
15, 16 pipe
2 second-type frame body
21 second internal space
22 second-type frame body
221 internal thread
223 external thread
7 cap body,
8 base
Number | Date | Country | Kind |
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2019-057730 | Mar 2019 | JP | national |
The present application is a continuation of International Application No. PCT/JP2020/009166, filed Mar. 4, 2020, which claims priority to Japanese Patent Application No. 2019-057730, filed Mar. 26, 2019, the entire contents of each of which being incorporated herein by reference.
Number | Date | Country | |
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Parent | PCT/JP2020/009166 | Mar 2020 | US |
Child | 17481693 | US |