» Articles » PMID: 25904929

Sarmentine, a Natural Herbicide from Piper Species with Multiple Herbicide Mechanisms of Action

Overview
Journal Front Plant Sci
Date 2015 Apr 24
PMID 25904929
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Sarmentine, 1-(1-pyrrolidinyl)-(2E,4E)-2,4-decadien-1-one, is a natural amide isolated from the fruits of Piper species. The compound has a number of interesting biological properties, including its broad-spectrum activity on weeds as a contact herbicide. Initial studies highlighted a similarity in response between plants treated with sarmentine and herbicidal soaps such as pelargonic acid (nonanoic acid). However, little was known about the mechanism of action leading to the rapid desiccation of foliage treated by sarmentine. In cucumber cotyledon disc-assays, sarmentine induced rapid light-independent loss of membrane integrity at 100 μM or higher concentration, whereas 3 mM pelargonic acid was required for a similar effect. Sarmentine was between 10 and 30 times more active than pelargonic acid on wild mustard, velvetleaf, redroot pigweed and crabgrass. Additionally, the potency of 30 μM sarmentine was greatly stimulated by light, suggesting that this natural product may also interfere with photosynthetic processes. This was confirmed by observing a complete inhibition of photosynthetic electron transport at that concentration. Sarmentine also acted as an inhibitor of photosystem II (PSII) on isolated thylakoid membranes by competing for the binding site of plastoquinone. This can be attributed in part to structural similarities between herbicides like sarmentine and diuron. While this mechanism of action accounts for the light stimulation of the activity of sarmentine, it does not account for its ability to destabilize membranes in darkness. In this respect, sarmentine has some structural similarity to crotonoyl-CoA, the substrate of enoyl-ACP reductase, a key enzyme in the early steps of fatty acid synthesis. Inhibitors of this enzyme, such as triclosan, cause rapid loss of membrane integrity in the dark. Sarmentine inhibited the activity of enoyl-ACP reductase, with an I 50app of 18.3 μM. Therefore, the herbicidal activity of sarmentine appears to be a complex process associated with multiple mechanisms of action.

Citing Articles

Label free quantitative proteomic analysis reveals the physiological and biochemical responses of Arabidopsis thaliana to cinnamon essential oil.

Kaab S, Martin M, Degand H, Foncoux B, Morsomme P, Jijakli M Sci Rep. 2025; 15(1):6156.

PMID: 39979395 PMC: 11842708. DOI: 10.1038/s41598-025-89368-4.


Genomic and Untargeted Metabolomic Analysis of Secondary Metabolites in the Strain MH191 Shows Media-Based Dependency for the Production of Bioactive Compounds with Potential Antifungal Activity.

Ramarajan M, Devilla R, Dow L, Walsh N, Mead O, Zakeel M J Agric Food Chem. 2024; 72(44):24432-24448.

PMID: 39440812 PMC: 11544706. DOI: 10.1021/acs.jafc.4c04989.


The effect of natural herbicide from Fusarium equiseti crude extract on the aquatic weed water hyacinth (Eichornia crassipes (Mart.) Solms).

Laosinwattana C, Manichart N, Thongbang M, Wichittrakarn P, Somala N, Teerarak M Sci Rep. 2024; 14(1):19542.

PMID: 39174667 PMC: 11341813. DOI: 10.1038/s41598-024-70694-y.


Functional mechanism study of the allelochemical myrigalone A identifies a group of ultrapotent inhibitors of ethylene biosynthesis in plants.

Heslop-Harrison G, Nakabayashi K, Espinosa-Ruiz A, Robertson F, Baines R, Thompson C Plant Commun. 2024; 5(6):100846.

PMID: 38460510 PMC: 11211550. DOI: 10.1016/j.xplc.2024.100846.


Plant Essential Oils as Biopesticides: Applications, Mechanisms, Innovations, and Constraints.

Gupta I, Singh R, Muthusamy S, Sharma M, Grewal K, Singh H Plants (Basel). 2023; 12(16).

PMID: 37631128 PMC: 10458566. DOI: 10.3390/plants12162916.


References
1.
Ohad N, Hirschberg J . Mutations in the D1 subunit of photosystem II distinguish between quinone and herbicide binding sites. Plant Cell. 1992; 4(3):273-82. PMC: 160128. DOI: 10.1105/tpc.4.3.273. View

2.
Li C, Tsai W, Damu A, Lee E, Wu T, Dung N . Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot. J Agric Food Chem. 2007; 55(23):9436-42. DOI: 10.1021/jf071963l. View

3.
Gonzalez-Thuillier I, Venegas-Caleron M, Garces R, von Wettstein-Knowles P, Martinez-Force E . Sunflower (Helianthus annuus) fatty acid synthase complex: enoyl-[acyl carrier protein]-reductase genes. Planta. 2014; 241(1):43-56. DOI: 10.1007/s00425-014-2162-7. View

4.
Ghose A, Crippen G . Atomic physicochemical parameters for three-dimensional-structure-directed quantitative structure-activity relationships. 2. Modeling dispersive and hydrophobic interactions. J Chem Inf Comput Sci. 1987; 27(1):21-35. DOI: 10.1021/ci00053a005. View

5.
Chen S, Xu X, Dai X, Yang C, Qiang S . Identification of tenuazonic acid as a novel type of natural photosystem II inhibitor binding in Q(B)-site of Chlamydomonas reinhardtii. Biochim Biophys Acta. 2007; 1767(4):306-18. DOI: 10.1016/j.bbabio.2007.02.007. View