JP5113092B2 - Propolis origin plant identification method - Google Patents

Description

The present invention relates to a propolis plant source identification how, in detail relates to the identification how the plant source of propolis using a primer pair comprising a specific nucleotide sequence.

  Propolis is a glue-like or wax-like substance made by mixing beeswax into plant exudates, shoots and resins collected by bees for the purpose of defense and reinforcement of the nest. This propolis contains various components because bees are produced by collecting various plants around the nest box as raw materials.

  Propolis mass has antibacterial and anti-inflammatory effects, as described in Aristotle's Animal Journal compiled in the 4th century BC as “therapeutic agent for skin diseases, cuts and infections” It has been known for a long time. Further, as the main physiological activity of propolis, for example, an antioxidant action, an immunostimulatory action, and an anticancer / antitumor action are known. For this reason, propolis has long been used as a raw material for medicines and health foods in Europe, but since 1985, it has been used in many products for prevention and treatment of diseases in addition to health foods and cosmetics. Came to be used.

  By the way, propolis production areas include South American countries such as China, Brazil, Argentina and Uruguay, Europe such as Hungary and Bulgaria, North America such as Canada, and Oceania such as Australia and New Zealand. In recent years, as disclosed in Non-Patent Document 1, many researchers have been researching the components contained in propolis by production area. Propolis is usually produced by leaving a bee hive in the field for days to months. Therefore, the plant origin which comprises a propolis by the difference of a surrounding plant is various, and it is thought that a content component changes greatly with the production areas. Propolis origin plants include, for example, plants such as asteraceae, cedar family, willow family, birch family, pine family, legume family, urushi family, and corn family. As disclosed in Patent Document 1, Brazilian propolis is composed of, for example, a perennial plant called Baccharis dracunculifolia (Baccharis dracunculifolia), which is a plant belonging to the genus Baccharis. It is known to be produced from substances collected from different plants. Brazilian propolis contains a large amount of cinnamic acid derivatives such as p-coumaric acid, artepilin C, and dulpanine as main components. For example, Artepilin C is abundantly contained in Brazilian propolis originating from Alexandrene, and is known to have an effective action of inducing apoptosis in tumor cells without causing side effects on the living body. From the above, it is considered that propolis differs in the appearance, properties, and components of propolis, and the expected action / function, depending on the type of plant material.

JP-T-2007-530433 (paragraph [0024])

Tazawa Shigemi et al .: Natural Medicines, 54 (6), 306-313, 2000

  In general, it is often difficult to accurately determine the origin plant as a raw material for propolis. For example, as a method for directly determining a source plant as a raw material for propolis, there is a method for capturing and tracking a scene where a bee collects a plant raw material. However, it is not possible to identify the origin plant from the propolis block after collection using such a method. Conventionally, methods for identifying the origin plant from the propolis bulk are the appearance, for example, color and properties, comparison of the components of the plant extract and the propolis extract as raw materials, and plant structure markers (for example, glandular hair) using a microscope. , Non-glandular hair, and shoot apical epidermal fragments) are known. However, such a method indirectly determines the plant material of origin, and has a problem that an accurate and reliable determination result may not be obtained because a determination experience is required.

  The present invention, for example, in Brazilian propolis, can be accurately performed using a PCR (Polymerase Chain Reaction) method using a specific primer in a method for determining whether or not the genus Baccaris is included as a propolis origin plant. It is based on the discovery of what can be done.

It is an object of the present invention is to provide an identification how the plant source of propolis can be accurately it is determined whether or not include Bakkarisu genus as the plant source of propolis.

  In order to achieve the above object, the propolis origin plant identification method according to the first aspect of the present invention is a template for propolis-derived DNA using at least one primer pair selected from the following (1) to (9): It is characterized by determining whether or not the genus Baccaris is included as a propolis origin plant by detecting a PCR product using the PCR reaction described above. (1) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6. (2) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 9. (3) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6. (4) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 2 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5. (5) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8. (6) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 3 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11. (7) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7. (8) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8. (9) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 10 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11.

  The invention according to claim 2 is characterized in that, in the method for identifying a plant of origin of propolis according to claim 1, the genus Baccharis is Baccharis dracunculifolia.

  The invention according to claim 3 is the method for identifying the plant of origin of propolis according to claim 1 or claim 2, wherein the primer pair is at least one primer pair selected from (5) to (9). It is characterized by being.

  According to the present invention, it is possible to accurately determine whether or not the genus Baccaris is included as a propolis origin plant.

An electrophoretic photograph of a PCR product when one kind of primer is used is shown (the photograph is subjected to black-and-white reversal processing for clarity). An electrophoresis photograph of a PCR product using each primer pair is shown (the photograph is subjected to black-and-white reversal processing for clarity).

Hereinafter, an embodiment embodying the method for identifying the plant of origin of propolis of the present invention will be described.
The propolis origin plant identification method of the present embodiment (hereinafter simply referred to as “identification method”) uses at least one primer pair selected from (1) to (9) described later as a template for propolis-derived DNA. It comprises the step of determining whether or not the genus Baccaris is contained by detecting the PCR product using the PCR reaction.

  Propolis is a glue-like or wax-like substance made by mixing saliva with plant exudates, shoots and resins collected by bees such as honey bees for the purpose of defense and reinforcement of the nest. Therefore, propolis contains DNA derived from collected plants. The propolis used in the identification method of the present embodiment is not particularly limited as long as it contains DNA, and preferably, a propolis bulk obtained from a nest box is used, and as long as it contains DNA derived from propolis, An extract obtained from the mass using an extraction solvent such as water or an organic solvent may be used as the specimen. The production area of the propolis used in the present embodiment is not particularly limited, but if a positive determination is expected, a propolis that is determined to have a possibility that the Brazilian plant or the main source plant is Asteraceae Buccaris is used. Is preferred. A preferable example of the genus Baccharis is Baccharis dracunculifolia (Baccharis dracunculifolia). Propolis originating from aleklen is rich in artepilin C having antitumor activity. For example, Brazilian propolis is known to be produced from substances collected from a plurality of plants, with arylene as the main plant.

  In the identification method of the present embodiment, it is preferable that a step of first extracting propolis-derived genomic DNA from a subject such as a propolis bulk is performed. As a method for extracting genomic DNA from a specimen, a method known in the field of molecular biology can be used, and purification may be performed as necessary. Examples of genomic DNA extraction methods include the silica-based resin type kit method (Promega Wizard DNA Clean-Up System), the silica gel membrane type kit method (QIAGEN DNeasy Plant Mini Kit revised method, NIPPON GENE GM quicker), and the CTAB method. It is done. Commercially available products include TRIzol Reagent manufactured by Invitrogen.

  Next, DNA amplification is performed using a PCR reaction using genomic DNA extracted from the subject as a template. As the primer pair used in this PCR reaction, at least one primer pair selected from the following (1) to (9) is used. (1) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6. This (1) primer pair amplifies 309 bp DNA of SEQ ID NO: 12. (2) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 9. This (2) primer pair amplifies the 263 bp DNA of SEQ ID NO: 13. (3) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6. This (3) primer pair amplifies 240 bp DNA of SEQ ID NO: 14. (4) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 2 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5. This (4) primer pair amplifies DNA of about 900 bp containing the nucleotide sequence of SEQ ID NO: 15. (5) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8. This (5) primer pair amplifies the 249 bp DNA of SEQ ID NO: 16. (6) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 3 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11. This (6) primer pair amplifies 238 bp DNA of SEQ ID NO: 17. (7) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7. This (7) primer pair amplifies 278 bp DNA of SEQ ID NO: 18. (8) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8. This (8) primer pair amplifies DNA of about 900 bp containing the nucleotide sequence of SEQ ID NO: 19. (9) The primer pair is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 10 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11. This (9) primer pair amplifies 267 bp DNA of SEQ ID NO: 20.

  As each primer pair of (1) to (9) above, the base sequences themselves of SEQ ID NOS: 1 to 11 constituting each primer pair can be used. In addition, each primer pair of the above (1) to (9) has a longer base sequence including each of SEQ ID NOS: 1 to 11, for example, a base following each base sequence is further about 5 to 20 bases (may be configured to be longer). (Possible) STS (Sequence tagged-site) primer or the like constituted by adding may be used. In the future, it is possible to construct an STS primer composed of 20 to 30 bases not including each base sequence among the bases following each base sequence. The STS can be determined from the nucleotide sequences of SEQ ID NOs: 12 to 20 amplified by each primer pair. By using STS, plants of the genus Baccharis can be more accurately (specifically) identified. For example, at both ends of SEQ ID NOs: 12 to 20 amplified by each primer pair, each base sequence of SEQ ID NOs: 1 to 11 (or a base sequence complementary to the sequence) and a sequence region (5 to 20) following the base sequence Primer composed of a base) or a primer composed of a sequence region (20 to 30 bases) following the base sequence.

  These primer pairs are RAPD (Random amplified polymorphic DNA) method (Williams. Et. Al. Nucleic Acids Research. Vol. 18, used as a method for detecting polymorphisms of nucleotide sequences between varieties. 6531, 1990). More specifically, when a DNA is amplified by PCR in the presence of a random primer, a primer or a primer pair that can distinguish between varieties is determined by the difference in size or number of genomic DNA amplified. Can do. In the present embodiment, the random primer may be synthesized using a DNA synthesizer, or commercially available products such as BEX common primers (A to D, F, Z set) may be used. Each of the primer pairs (1) to (9) determined by the RAPD method is designed to be suitable for identification of the genus Baccaris that is a source plant constituting the propolis. Among these, at least one primer pair selected from (5) to (9) is preferable because it can more specifically identify the genus Baccharis.

  For amplification of genomic DNA using PCR, known methods can be appropriately employed. PCR reaction using each primer pair of (1) to (9) is carried out in accordance with conventional methods, template DNA dissociation step, primer-template DNA annealing step, and complementary strand synthesis by DNA polymerase using the primer as a starting point. It is performed by repeating a DNA replication cycle consisting of steps. The PCR reaction solution is, for example, DNA derived from propolis as template DNA, the primer pair of any of (1) to (9), heat-resistant DNA polymerase (for example, Tag polymerase), dNTPs (dATP, dTTP, dCTP, dGTP) ), And a reaction buffer or the like. The template DNA dissociation step is preferably performed at 90 to 100 ° C. for several seconds to several minutes, and the primer and template DNA annealing step is preferably performed at 38 to 50 ° C. for about 30 seconds to 3 minutes. The complementary strand synthesis step is preferably performed at 70 to 73 ° C. for about 30 seconds to 6 minutes. The number of repetitions of the DNA replication cycle is not particularly limited, but is preferably 30 to 60 times, more preferably 40 to 50 times. The DNA replication cycle can be performed using a commercially available PCR apparatus.

  By repeating the above-described replication cycle, a target PCR product (amplified genomic DNA) can be obtained. PCR products are detected by a DNA separation step and a DNA detection step. The DNA separation step can be performed using, for example, agarose gel electrophoresis, polyacrylamide gel electrophoresis, capillary electrophoresis, or the like. The DNA detection step can be detected using, for example, a phenanthridine dye such as ethidium bromide. For example, ethidium bromide binds to nucleic acid and emits fluorescence proportional to the amount of DNA when irradiated with ultraviolet light. Alternatively, the primer molecule may be synthesized in advance using a labeled molecule (for example, a fluorescent molecule, a dye molecule, a radioisotope, etc.) or added with the labeled molecule, and detected using a known method.

  Whether or not the genus Baccaris is included as a propolis origin plant is determined based on the fractionation pattern obtained through the steps of separation and detection of the PCR product generated by the replication cycle. Comparative analysis of PCR product fractionation patterns is performed based on the presence or absence of amplified genomic DNA, molecular weight (number of bases), amount, base sequence, and the like. They can be determined by analyzing the presence / absence of a band when electrophoresing a PCR product, a moving distance, light and shade, and a base sequence.

  In order to more accurately determine whether or not a plant derived from the genus Buccaris is contained in propolis, it is preferable to repeat the PCR reaction two or more times, and perform the PCR reaction using two or more primer pairs. More preferably, the PCR product is detected.

According to the propolis origin plant identification method of the present embodiment, the following effects can be obtained.
The propolis origin plant identification method of the present embodiment uses a PCR reaction using at least one primer pair selected from the above (1) to (9) and a DNA derived from propolis as a template. By detecting, it is determined whether or not the genus Baccaris is included as a propolis origin plant. Therefore, it is possible to accurately determine whether or not the genus Baccaris is included as a propolis origin plant.

  -By the propolis origin plant identification method of the present embodiment, the plants belonging to the genus Bucaris genus and other propolis origin plants, which are known as the origin plant of the asteraceae, willow family, birch family, pine family, legume family, urushi family, It can be distinguished from plants such as Myrtaceae.

  -According to the identification method of this embodiment, Brazilian propolis and the other propolis are known as the origin of Brazilian propolis and other propolis, the main plant of which is Asteraceae Buccaris, Europe such as Hungary, Bulgaria, It can be distinguished from North American countries such as Canada, Oceania such as Australia and New Zealand.

-The identification method of the origin plant of the propolis of this embodiment can be preferably applied by the identification of Alekrene (Baccharis dracunculifolia).
・ For example, Brazilian propolis containing a lot of aleklen is called green propolis because the propolis bulk is a little greenish. According to the method for identifying the plant of origin of propolis of the present embodiment, green propolis can be directly and accurately identified and determined as well as a sensory identification only for appearance.

  -In the identification method of the propolis origin plant of this embodiment, Preferably at least 1 type of primer pair chosen from said (5)-(9) is used. Therefore, it is possible to determine whether or not the genus Baccaris is included as a propolis origin plant more accurately and reliably.

  -The identification method of the plant of origin of the propolis of this embodiment can be implemented by applying well-known molecular biological techniques, such as PCR method and electrophoresis method. Therefore, it can be implemented easily and the result can be easily judged.

In addition, you may change the said embodiment as follows.
-As a reference form, the PCR reaction using DNA derived from propolis as a template, and detecting the PCR product, the above (1) to (1) to determine whether or not the genus Baccaris is included as a propolis origin plant You may comprise as a primer set for DNA amplification which consists of at least 1 type of primer pair chosen from 9).

  The primer set for DNA amplification is further configured as a propolis origin plant identification kit comprising a nucleic acid amplification reagent such as a DNA polymerase, a dNTPs mixture, a nucleic acid amplification reaction buffer, and a genomic DNA extraction reagent. May be.

  -In this embodiment, the density of the detection band when the PCR product is electrophoresed, or the comparison of the relative values thereof, not only the presence or absence of a plant belonging to the genus Buccaris in propolis but also the content, content, etc. in the whole are calculated. May be.

Examples are given below to describe the above embodiments more specifically, but the present invention is not limited to these examples.
<Test Example 1: Examination of whether or not DNA of the genus Buccaris is contained in green propolis>
(Test sample)
Propolis (brazilian green propolis: A and B used by two companies) collected from a nest box in which the surrounding plants were mainly composed of aleklen was used as a test sample. Aleklen (Baccaris) as a positive control, peripheral plants other than Aleklen as a negative control (1) Cypresti, (2) Paranna, (3) Pororoca, (4) Aloeira fresh leaves, and African bee honey bees ( DNA from Brazil) was used.

(DNA extraction)
DNA extraction from propolis, plant leaves, and bees was performed using TRIzol Reagent (Invitrogen). Plant tissues were weighed into 50 mg to 100 ng, 2 mL Eppendorf tubes. 1 mL of TRIzol Reagent was added and mixed. 300 μL of chloroform was added, and the mixture was mixed by inversion for about 15 seconds, and left at room temperature for 2 to 3 minutes. These were centrifuged at 5000-5500 rpm for 15 minutes at low temperature, and the upper layer was discarded. 450 μL of ethanol was added, mixed by inversion, and left at room temperature for 2 to 3 minutes. Centrifuged at 2500 rpm for 5 minutes, and the upper layer (phenol-ethanol layer) was discarded. To this, 1 mL of 0.1 M sodium citrate-10% ethanol was added and mixed by inverting at room temperature for 30 minutes. Centrifuged at 2500 rpm for 5 minutes, and the upper layer was discarded. 1.5-2.0 mL of 75% ethanol was added, and mixed by inverting at room temperature for 30 minutes. Centrifuged at 2500 rpm for 5 minutes, and the upper layer was discarded. The Eppendorf tube is air-dried for about 15 to 30 minutes and diluted with 300 to 600 μL of 8 mM NaOH. The whole was diluted 20-fold into TE to make 30 μL to 600 μL. The spectrum was measured by ultraviolet absorbance measurement (230 to 320 nm), and it was confirmed that there was a peak near 257 nm.

(PCR amplification and detection of PCR product using RAPD marker)
The RAPD (Random amplified polymorphic DNA) method is used to detect the polymorphism between the plant origins of the band amplified using a random primer, and a clear and reproducible polymorphism is selected from the detected polymorphism.

  PCR amplification was performed using genomic DNA extracted from each test sample as a template and random primers for the RAPD method. As a random primer, BEX common primer A set (100 types) was used as a single primer.

  The composition of the PCR reaction solution was 2.5 μL of 10 × PCR buffer, 2.0 μL of 2.5 mM dNTP mixed solution, 1.6 μL of 7.8 μM random primer, 0.2 μL of 5 U / μL rTaq polymerase (manufactured by TAKARA) ), 1.0 μL of 5 ng / μL template genomic DNA, and 17.7 μL of sterilized water to a total volume of 25.0 μL. PCR was performed by a thermal cycler (Gene Amp PCR System manufactured by PERKIN ELMER CETUS) at 98 ° C. for 5 minutes, followed by 45 cycles of 98 ° C. for 10 seconds, 40 ° C. for 1 minute, and 72 ° C. for 1 minute. After keeping the temperature in minutes, the temperature was kept at 4 ° C.

  After the reaction, the PCR product was electrophoresed on a 2.0% agarose gel in 0.5 × TBE buffer, stained with ethidium bromide, and then a band was detected under UV light. Among the detected bands, a band (RAPD marker) showing a clear and reproducible polymorphism was selected. The result is shown in FIG. 1 (FIG. 1 shows the result of only one kind of primer).

  As shown in FIG. 1, by using the BEX common primer A set, a band at the same level as that of the plant belonging to the genus Buccaris was detected in green propolis. In addition, the band of the same level was not detected from other surrounding plants and genes derived from bees. Similar results were obtained for 11 types of single primers shown in SEQ ID NOs: 1 to 11 in the BEX common primer A set. It was confirmed that the green propolis contained DNA belonging to the genus Baccharis.

<Test Example 2: Examination of primer pair>
As test samples, raw leaves of Aleklen (Baccaris), Cypressi, Parana pine, Pororocca, and Aloeira were used as propolis raw materials, and African bee honey bees (Brazilian) and Western honey bees (Chinese) were used as bees. As a primer, 2 types were selected from 11 types of primers shown in SEQ ID NOs: 1 to 11 in which bands of the same level as those of plants belonging to the genus Buccaris were detected in Green Propolis in Test Example 1, and double primers (primer pair: All 55 pairs were examined). Note that the method described in Test Example 1 was applied as a method for detecting a band by DNA extraction, PCR, and electrophoresis. Further, the base sequence of the fragment amplified by PCR was determined according to the following method. The result of electrophoresis after PCR is shown in FIG.

(Determination of the base sequence of the amplified fragment)
Among the DNA fragments amplified from each primer pair, DNA fragments that were good for discrimination of Baccaris were selected. Those DNA fragments were purified using QIAprep Spin Miniprep Kit (manufactured by QIAGEN). The purified amplified DNA was subjected to nucleotide sequencing by entrusting it to Sigma-Aldrich Japan.

  As shown in FIG. 2, when using the primer pairs (1) to (9) above, an acrelen-specific band belonging to the genus Baccharis was detected. (1) A 309 bp PCR product consisting of the base sequence of SEQ ID NO: 12 is obtained by the primer pair. (2) A 263 bp PCR product consisting of the base sequence of SEQ ID NO: 13 is obtained by the primer pair. (3) A 240 bp PCR product consisting of the base sequence of SEQ ID NO: 14 is obtained by the primer pair. (4) A PCR product of about 900 bp containing the nucleotide sequence of SEQ ID NO: 15 is obtained by the primer pair. In addition, since the PCR product of about 900 bp obtained by this (4) primer pair has a long sequence, the base sequence is determined only at the central portion of the entire sequence. The determined base sequence is shown in SEQ ID NO: 15. (5) A 249 bp PCR product consisting of the base sequence of SEQ ID NO: 16 is obtained by the primer pair. (6) A 238 bp PCR product consisting of the base sequence of SEQ ID NO: 17 is obtained by the primer pair. Although close bands are detected in African bee and Western bees, there is no problem with discrimination. In addition, certainty is high. (7) A 278 bp PCR product consisting of the base sequence of SEQ ID NO: 18 is obtained by the primer pair. A close band is detected in the African bee honeybee, but there is no problem in discrimination. (8) A PCR product of about 900 bp containing the nucleotide sequence of SEQ ID NO: 19 is obtained by the primer pair. In addition, since the PCR product of about 900 bp obtained by this (8) primer pair has a long sequence, the base sequence is determined only at the central portion of the entire sequence. The determined base sequence is shown in SEQ ID NO: 19. (9) A 267 bp PCR product consisting of the base sequence of SEQ ID NO: 20 is obtained by the primer pair. A close band is detected in the Aloeira, but there is no problem in discrimination. In addition, certainty is high.

  Among these primer pairs, those having particularly good reproducibility were the primer pairs (5) to (9). Considering the ease of discrimination, the primer pairs (5) and (8) are more preferable.

  As described above, by using a specific primer pair, it is possible to directly determine the origin plant of the propolis by detecting whether or not a gene derived from the genus Baccaris is included from the gene product in the propolis. It was.

Next, technical ideas that can be grasped from the above-described embodiment and other examples will be described below together with their effects.
(A) A propolis-origin plant identification kit further comprising a DNA polymerase, a dNTPs mixture, a nucleic acid amplification reaction buffer, and a genomic DNA extraction reagent as a nucleic acid amplification reagent in the primer set.

  (B) The propolis characterized by calculating the content ratio or content of the entire plant of the genus Buccaris in the propolis by comparing the density of the detection band when the PCR product is electrophoresed or the relative value thereof. To identify plant origin.

Claims (3)

By using a PCR reaction using at least one primer pair selected from the following (1) to (9) and a DNA derived from propolis as a template, and detecting a PCR product, the plant of Propolis is included as a source plant of propolis. A method for identifying a propolis origin plant, characterized by determining whether or not.
(1) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6.
(2) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 9.
(3) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 6.
(4) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 2 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 5.
(5) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 1 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8.
(6) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 3 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11.
(7) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 7.
(8) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 4 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 8.
(9) A primer pair which is a combination of an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 10 and an oligonucleotide primer containing the base sequence shown in SEQ ID NO: 11.   2. The method for identifying a propolis origin plant according to claim 1, wherein the genus Baccharis is Aleklen (Baccharis dracunculifolia).   The said primer pair is at least 1 type of primer pair chosen from said (5)-(9), The identification method of the origin plant of the propolis of Claim 1 or Claim 2 characterized by the above-mentioned.