Allelopathic Activity of Annona reticulata L. Leaf Extracts and Identification of Three Allelopathic Compounds for the Development of Natural Herbicides

被引:6
作者
Khatun, Mst. Rokeya [1 ,2 ,3 ]
Tojo, Shunya [4 ]
Teruya, Toshiaki [5 ]
Kato-Noguchi, Hisashi [1 ,2 ]
机构
[1] Kagawa Univ, Fac Agr, Dept Appl Biol Sci, Miki, Kagawa 7610795, Japan
[2] Ehime Univ, United Grad Sch Agr Sci, 3-5-7 Tarumi, Matsuyama 7908566, Japan
[3] Bangladesh Agr Univ, Fac Agr, Mymensingh 2202, Bangladesh
[4] Univ Ryukyus, Grad Sch Engn & Sci, 1 Senbaru, Nishihara, Okinawa 9030213, Japan
[5] Univ Ryukyus, Fac Educ, 1 Senbaru, Nishihara, Okinawa 9030213, Japan
来源
AGRONOMY-BASEL | 2022年 / 12卷 / 11期
关键词
Annona reticulata; weed control; loliolide; 5-hydroxy-3; 4-dimethyl-5-pentylfuran-2(5H)-one; 3; 4-dihydroxyphenylethanol; ANTIOXIDANT ACTIVITY; PHENOLIC-COMPOUNDS; WEED-CONTROL; SUBSTANCES; FRACTIONS; ACID;
D O I
10.3390/agronomy12112883
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Using plant-based allelopathic compounds might be a potent substitute to help mitigate the effects of synthetic herbicides. Annona reticulata L. is often planted for its fruit in residential gardens. This plant is well-documented for its diverse ethnomedicinal uses. However, there is no information in the literature on the allelopathic potential of A. reticulata leaves. Therefore, the allelopathic potential and relevant allelopathic compounds of A. reticulata leaves were investigated in this study. The bioassays were carried out using a completely randomized experimental layout (CRD), and the resulting data were analyzed using one-way ANOVA at p <= 0.05. Aqueous methanol extracts of A. reticulata leaves significantly inhibited the growth of three dicots and three monocots (Lepidium sativum L., Medicago sativa L., Lactuca sativa L., Echinochloa crus-galli (L.) P. Beauv., Lolium multiflorum Lam., and Phleum pratense L., respectively). The level of growth inhibition was proportional to the A. reticulata extract concentration. Three compounds were purified through different chromatographic steps, and their structures were determined using spectroscopy and identified as loliolide, 5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5H)-one, and 3,4-dihydroxyphenylethanol. The 5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5H)-one had the greatest effect on suppressing cress root growth, while loliolide had the greatest effect on suppressing timothy shoot growth. The values for 50% seedling growth suppression showed that the compound with the maximum inhibitory activity was loliolide, followed by 5-hydroxy-3,4-dimethyl-5-pentylfuran-2(5H)-one and 3,4-dihydroxyphenylethanol. Therefore, this result suggests that the three compounds might be responsible for the allelopathic effects of A. reticulata leaf extracts, and these compounds have the potential to be used to develop effective bioherbicides.
引用
收藏
页数:13
相关论文
共 71 条
  • [1] Abdul Khaliq Abdul Khaliq, 2010, Pakistan Journal of Weed Science Research, V16, P409
  • [2] [Anonymous], 1987, FRUITS WARM CLIMATES
  • [3] Bachheti A., 2020, COEVOLUTION SECONDAR, P441
  • [4] The role of root exudates in rhizosphere interations with plants and other organisms
    Bais, Harsh P.
    Weir, Tiffany L.
    Perry, Laura G.
    Gilroy, Simon
    Vivanco, Jorge M.
    [J]. ANNUAL REVIEW OF PLANT BIOLOGY, 2006, 57 : 233 - 266
  • [5] Antioxidant activity of tocopherols and phenolic compounds of virgin olive oil
    Baldioli, M
    Servili, M
    Perretti, G
    Montedoro, GF
    [J]. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1996, 73 (11) : 1589 - 1593
  • [6] Bari IN, 2017, ACTA AGROBOT, V70, DOI 10.5586/aa.1720
  • [7] Analgesic and Antiinflammatory Activity of Kaur-16-en-19-oic acid from Annona reticulata L. Bark
    Chavan, Machindra J.
    Kolhe, Dinesh R.
    Wakte, Pravin S.
    Shinde, Devanand B.
    [J]. PHYTOTHERAPY RESEARCH, 2012, 26 (02) : 273 - 276
  • [8] A COMPREHENSIVE REVIEW ON ANNONA RETICULATA
    Chavan, Shital S.
    Shamkuwar, Prashant B.
    Damale, Manoj G.
    Pawar, Deepak P.
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2014, 5 (01): : 45 - 50
  • [9] Investigating the mode of action of natural phytotoxins
    Dayan, FE
    Romagni, JG
    Duke, SO
    [J]. JOURNAL OF CHEMICAL ECOLOGY, 2000, 26 (09) : 2079 - 2094
  • [10] Natural Compounds as Next-Generation Herbicides
    Dayan, Franck E.
    Duke, Stephen O.
    [J]. PLANT PHYSIOLOGY, 2014, 166 (03) : 1090 - 1105