全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Evaluation of Isoflavones as Allelochemicals with Strong Allelopathic Activities of Kudzu Using Protoplast Co-Culture Method with Digital Image Analysis

DOI: 10.4236/ajps.2021.123024, PP. 376-393

Keywords: Allelopathy, Bioassay, Daidzein, Isoflavone, Protoplast Culture, Puerarin

Full-Text   Cite this paper   Add to My Lib

Abstract:

The inhibitory allelopathic activity of Pueraria montana (Kudzu), and activities of two putative allelochemical isoflavones, puerarin and daidzein, were evaluated using the protoplast co-culture method with digital image analysis using lettuce as a recipient (DIA-PP method). Cotyledon protoplasts of Kudzu were isolated using Cellulase R10 and Driselase 20 in 0.6 M mannitol solution. Optimal hormonal condition and density for growth of Kudzu protoplasts were surveyed. Medium for co-culture of Kudzu or isoflavones with lettuce protoplasts was 50 μl liquid MS basal medium containing 1 μM 2,4-dichlorophenoxyacetic acid, 0.1 μM benzyladenine, 3% sucrose, and 0.4 M or 0.6 M mannitol. Protoplast division of lettuce was strongly inhibited by Kudzu at a low density (104/ml). Slightly less inhibition by Kudzu on cell wall formation and yellow pigment accumulation stages of lettuce growth was also observed. Puerarin did not inhibit the growth of lettuce protoplasts at three growth stages but slightly stimulated growth at high concentrations. By contrast, daidzein, aglycon of puerarin, inhibited growth at three stages of lettuce protoplast growth and strongly inhibited cell division at 100 μM. Daidzein might be one cause of the strong inhibitory allelopathic activity of Kudzu. Grade of inhibitory activities was compared with that of other allelopathic plants including an invader plant and their allelochemicals studied using the DIA-PP method.

References

[1]  Gulizia, J.P. and Downs, K.M. (2019) A Review of Kudzu’s Use and Characteristics as Potential Feedstock. MDPI Agriculture, 9, 220.
https://doi.org/10.3390/agriculture9100220
[2]  Liu, H.L. and Li, L. (2002) Cell Cultures of Pueraria lobata (Willd.): Growth and Production of Isoflavones and Puerarin. South African Journal of Botany, 68, 542-544.
https://doi.org/10.1016/S0254-6299(15)30382-3
[3]  Kirakosyan, A., Kaufman, P.B., Warber, S., Bolling, S. and Duke, J.A. (2003) Quantification of Major Isoflavonoids and L-canavanine in Several Organs of Kudzu Vine (Pueraria montana) and in Starch Samples Derived from Kudzu Roots. Plant Science, 164, 883-888.
https://doi.org/10.1016/S0168-9452(03)00077-3
[4]  Chen, T.R., Shih, S.C., Ping, H.P. and Wei, Q.K. (2012) Antioxidant Activity and Isoflavonoid Components in Different Sections of Pueraria lobata Root. Journal of Food and Drug Analysis, 20, 681-685.
[5]  Shimizu, H., Tsuduki, M. and Matsuzawa, K. (2007) Isoflavonoids in the Stalk of Pueraria lobata Ohwi. Report of Nara Prefectural Institute of Industrial Technology, 33, 46-48.
[6]  Kimura, K., Yamabe, T., Inoue, T. and Kitada, Y. (2011) Investigations of the Amount of Isoflavones Contained in Kuzu Starches and Kuzu Leaves. Japanese Journal of Food Chemistry and Safety, 18, 48-52.
[7]  Takeya, K. and Itokawa, H. (1982) Isoflavonoids and the Other Constituents in Callus Tissues of Pueraria lobata. Chemical and Pharmaceutical Bulletin, 30, 1496-1499.
https://doi.org/10.1248/cpb.30.1496
[8]  Hakamatsuka, T., Shinkai, K., Noguchi, H., Ebizuka, Y. and Sankawa, U. (1992) Isoflavone Dimers from Yeast Extract-Treated Cell Suspension Cultures of Pueraria lobata. Zeitshrift fur Naturforschung, 47c, 177-182.
https://doi.org/10.1515/znc-1992-3-402
[9]  Bergum, K., Shammi, M., Hasan, N., Asaduzzaman, M., Appiah, K.S. and Fujii, Y. (2019) Potential Allelopathic Candidates for Land Use and Possible Sustainable Weed Management in South Asian Ecosystem. Sustainability, 11, 2649.
https://doi.org/10.3390/su11092649
[10]  Itani, T., Hirai, K., Fujii, Y., Kohdai, H. and Tamaki, M. (1998) Screening for Allelopathic Activity among Weeds and Medicinal Plants Using the “Sandwich Method”. Journal of Weed Science and Technology, 43, 258-266.
https://doi.org/10.3719/weed.43.258
[11]  Fujii, Y., Parvez, S.S., Parvez, M.M., Ohmae, Y. and Iida, O. (2003) Screening of 239 Medicinal Plant Species for Allelopathic Activity Using the Sandwich Method. Weed Biology and Management, 3, 233-241.
https://doi.org/10.1046/j.1444-6162.2003.00111.x
[12]  Fujii, Y., Shibuya, T., Nakatani, K., Itani, T., Hiradate, S. and Parvez, M.M. (2004) Assessment Method for Allelopathic Effect from Leaf Litter Leachates. Weed Biology and Management, 4, 19-23.
https://doi.org/10.1111/j.1445-6664.2003.00113.x
[13]  Fujii, Y. and Hiradate, S. (2003) Research Achievement of Allelopathy Laboratory in NIAES, from 1983 to 2001. Part 2. National Institute for Agro-Environmental Sciences (NIAES), Ibaraki, 579-1180.
[14]  Fujii, Y., Pariasca, D., Shibuya, T., Yasuda, T., Kahn, B. and Waller, G.R. (2007) Plant Box Method: A Specific Bioassay to Evaluate Allelopathy through Root Exudates. In: Fujii, Y. and Hiradate, S., Eds., Allelopathy New Concepts and Methodology, 2nd Edition, Science Publishers, Inc., Enfield, 39-56.
[15]  Fujii, Y. (1999) Significance of Allelopathy as a Factor of Biodiversity and Its Application to Agriculture. In: Techno Innovation, Japan Association for Techno-Innovation in Agriculture, Forestry and Fisheries, Tokyo, 9(2), 27-32.
[16]  Sasamoto, H., Murashige-Baba, T., Inoue, A., Sato, T., Hayashi, S. and Hasegawa, A. (2013) Development of a New Method for Bioassay of Allelopathy Using Protoplasts of a Leguminous Plant Mucuna pruriens with a High Content of the Allelochemical L-DOPA. Journal of Plant Studies, 2, 71-80.
https://doi.org/10.5539/jps.v2n2p71
[17]  Sasamoto, H., Mardani, K.H., Sasamoto, Y., Wasano, N., Murashige-Baba, T., Sato, T., Hasegawa, A. and Fujii, Y. (2019) Evaluation of Canavanine as an Allelochemical in Etiolated Seedlings of Vicia villosa Roth: Protoplast Co-Culture Method with Digital Image Analysis. In Vitro Cellular and Developmental Biology-Plant, 55, 296-304.
https://doi.org/10.1007/s11627-019-09985-3
[18]  Mori, D., Ogita, S., Fujise, K., Inoue, A. and Sasamoto, H. (2015) Protoplast Co-Culture Bioassay for Allelopathy in Leguminous Plants, Leucaena leucocephala and Mucuna gigantea, Containing Allelochemical Amino Acids, Mimosine and L-DOPA. Journal of Plant Studies, 4, 1-11.
https://doi.org/10.5539/jps.v4n1p1
[19]  Inoue, A., Mori, D., Minagawa, R., Fujii, Y. and Sasamoto, H. (2015) Allelopathy in a Legu Minous Mangrove Plant, Derris indica: Protoplast Co-Culture Bioassay and Rotenone Effect. Natural Product Communications, 10, 747-750.
https://doi.org/10.1177/1934578X1501000512
[20]  Fujise, K., Yokota, S. and Sasamoto, H. (2018) Evaluation of Allelochemicals, Abscisic Acid and Coumarin, in Leaf-Origin Suspension Cultured Cells of Prunus yedoensis Using Protoplast Co-Culture Bioassay Method. American Journal of Plant Sciences, 9, 172-184.
https://doi.org/10.4236/ajps.2018.92015
[21]  Hasegawa, A., Oyanagi, T., Minagawa, R., Fujii, Y. and Sasamoto, H. (2014) An Inverse Relationship between Allelopathic Activity and Salt Tolerance in Suspension Cultures of Three Mangrove Species, Sonneratia alba, S. caseolaris and S. ovata: Development of a Bioassay Method for Allelopathy, the Protoplast Co-Culture Method. Journal of Plant Research, 127, 755-761.
https://doi.org/10.1007/s10265-014-0651-1
[22]  Sasamoto, H., Azumi, Y. and Suzuki, S. (2017) Development of a High-Throughput Bioassay Method of Allelopathy: Protoplast Co-Culture and Digital Image Analysis. Science Journal of Kanagawa University, 28, 63-70.
[23]  Sasamoto, H., Azumi, Y., Shimizu, M., Hachinohe, Y. and Suzuki, S. (2017) In Vitro Bioassay of Allelopathy of Arabidopsis thaliana by Sandwich Method and Protoplast Co-Culture Method with Digital Image Analysis. Plant Biotechnology, 34, 199-202.
https://doi.org/10.5511/plantbiotechnology.17.1204a
[24]  Ogita, S. and Sasamoto, H. (2017) In Vitro Bioassay of Allelopathy in Four Bamboo Species; Bambusa multiplex, Phyllostachys bambusoides, P. nigra, Sasa kurilensis, Using Sandwich Method and Protoplast Co-Culture Method with Digital Image Analysis. American Journal of Plant Sciences, 8, 1699-1710.
https://doi.org/10.4236/ajps.2017.87117
[25]  Sasamoto, H., Iwashina, T., Suzuki, S., Azumi, Y. and Fujii, Y. (2018) Evaluation of an Anthocyanin, Cyanidin 3,5-di-O-glucoside, as an Allelochemical in Red Callus of a Mangrove Sonneratia ovata, Using Protoplast Co-Culture Bioassay Method with Digital Image Analysis. Journal of Plant Studies, 7, 1-10.
https://doi.org/10.5539/jps.v7n2p1
[26]  Suzuki, S., Wasano, N., Kimura, M., Yasuda, R., Nakagawa, W., Sasamoto, Y., Fujii, Y. and Sasamoto, H. (2018) Evaluation of Putative Allelochemicals, Cinnamic Acid and an Anthocya Nin, in Spiraea thunbergii and S. cantoniensis Using in Vitro Bioassay Method of Allelopathy, the Protoplast Co-Culture with Digital Image Analysis. Proceedings of the 4th International Conference of Asian Allelopathy Society, Tokyo, 33, 72.
[27]  Sasamoto, H., Hayatsu, M. and Suzuki, S. (2020) High Allelopathic Activity of Carotenoid-Accumulating Callus of a Halophilic Mangrove Plant, Avicennia alba: Protoplast Co-Culture Method with Digital Image Analysis. Journal of Plant Studies, 9, 1-12.
https://doi.org/10.5539/jps.v9n1p1
[28]  Sasamoto, H., Fujii, Y. and Ashihara, H. (2015) Effect of Purine Alkaloids on the Proliferation of Lettuce Cells Derived from Protoplasts. Natural Product Communications, 10, 751-754.
https://doi.org/10.1177/1934578X1501000513
[29]  Ogita, S. and Sasamoto, H. (2018) In Vitro Bioassay of Allelopathy in Caffeine-Containing Coffee Cells Using Protoplast Co-Culture Method with Digital Image Analysis. Proceedings of the 4th International Conference of Asian Allelopathy Society, Tokyo, 13, 52.
[30]  Ogita, S., Asrori, M.I. and Sasamoto, H. (2020) Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method. Plants (MDPI), 9, 1170.
https://doi.org/10.3390/plants9091170
[31]  Mardani-Korrani, H., Sasamoto, H., Suzuki, S., Sasamoto, Y. and Fujii, Y. (2020) Application of the Protoplast Co-Culture Method for Evaluation of Allelopathic Activities of Volatile Compounds Safranal and Tulipalin A. Results in Chemistry, 2, 1-5.
https://doi.org/10.1016/j.rechem.2020.100030
[32]  Murashige, T. and Skoog, F. (1962) A Revised Medium for Rapid Growth and Bioassays with Tobacco Tissue Cultures. Physiologia Plantarum, 15, 473-497.
https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
[33]  Rasband, W.S. (1997-2016) Image J. U.S. National Institute of Health, Bethesda, Maryland, USA.
https://imagej.nih.gov/ij
[34]  Sasamoto, H., Suzuki, S., Mardani-Korrani, H., Sasamoto, Y. and Fujii, Y. (2021) Allelopathic Activities of Three Carotenoids, Neoxanthin, Crocin and β-Carotene, Assayed Using Protoplast Co-Culture Method with Digital Image Analysis. Plant Biotechnology, 38.
https://doi.org/10.5511/plantbiotechnology.20.1211a
[35]  Sasamoto, H. and Ashihara, H. (2014) Effect of Nicotinic Acid, Nicotinamide and Trigonelline on the Proliferation of Lettuce Cells Derived from Protoplasts. Phytochemistry Letters, 7, 38-41.
https://doi.org/10.1016/j.phytol.2013.09.008
[36]  Tamura, S., Chang, C.F. and Suzuki, A. (1969) Chemical Studies on “Clover Sickness”. Part I. Isolation and Structural Elucidation of Two New Isoflavonoids in Red Clover. Agricultural and Biological Chemistry, 33, 391-397.
https://doi.org/10.1080/00021369.1969.10859321
[37]  Chang, C.F., Suzuki, A., Kumai, S. and Tamura, S. (1969) Chemical Studies on “Clover Sickness”. Part II. Biological Functions of Isoflavonoids and Their Related Compounds. Agricultural and Biological Chemistry, 33, 398-408.
https://doi.org/10.1080/00021369.1969.10859325
[38]  Rashid, M.H., Asaeda, T. and Uddin, M.N. (2010) The Allelopathic Potential of Kudzu (Pueraria pueraria). Weed Science, 58, 47-55.
https://doi.org/10.1614/WS-09-106.1
[39]  Oshima, A., Mine, W., Nakada, M. and Yanase, E. (2016) Analysis of Isoflavones and Coumestrol in Soybean Sprouts. Bioscience, Biotechnology, and Biochemistry, 80, 2077-2079.
https://doi.org/10.1080/09168451.2016.1196577
[40]  Sugiyama, A., Yamazaki, Y., Hamamoto, S., Takase, H. and Yazaki, K. (2017) Synthesis and Secretion of Isoflavones by Field-Grown Soybean. Plant and Cell Physiology, 58, 1594-1600.
https://doi.org/10.1093/pcp/pcx084
[41]  Okutani, F., Hamamoto, S., Aoki, Y., Nakayasu, M., Nihei, N., Nishimura, T., Yazaki, K. and Sugiyama, A. (2019) Rhizosphere Modeling Reveals Spatiotemporal Distribution of Daidzein Shaping Soybean Rhizosphere Bacterial Community. Plant, Cell and Environment, 43, 1036-1046.
https://doi.org/10.1111/pce.13708
[42]  Kato-Noguchi, H. (2003) Allelopathic Substances in Pueraria thunbergiana. Phytochemistry, 63, 577-580.
https://doi.org/10.1016/S0031-9422(03)00195-X
[43]  Kobayashi, K., Sasamoto, H. and Fujii, Y. (2020) Search and Evaluation of Substances; to Control the Twining Weeds. Proceedings of the 59th Weed Science Society of Japan (WSSJ) Annual Meeting, Nagano, 11-12 April 2020, 27, 97.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133