Activity of 11 antifungal plants on
Abstract
Plants produce secondary metabolites that are essential for survival of the producing plants such as to attract insect for pollination and defend against pest and environmental stress. Plant secondary metabolites are widely exploited by the mankind especially for medicine, one of which is to protect against infection by microorganism including fungi. Many medicinal plants have been traditionally used and/or studied for the fungicidal activity. Most of the plants studied or traditionally used as antifungi show antiphytophthora activity and some of them also active as antifusarium. Higher concentration plant extract is needed to inhibit the growth of Fusarium than Phytophthora. Considering the concentration in plant and activity as antifungi, eugenol is considered to be the most effective to be used as antiphytophthora and antifusarium. The presence of aromatic moiety, orthodioxy substitution, and double bond in the terminal of site chain is considered to be essential for the antifungal activity of the eugenol derivative.
Keywords
- secondary metabolites
- plant
- antifungal
- antifusarium
- antiphytophthora
1. Introduction
Plants conduct primary metabolism to support the growth and development. In addition to primary metabolism, plant also produce and collect secondary metabolites. Compared to primary metabolites that are found in every organism, secondary metabolite has limited distribution, has been produced and collected in specific organ, and has no physiological role in the producing plants. Secondary metabolites may function in protecting the producing plant from pests and facilitate plant breeding by spreading seeds through organisms consuming fruits produced by the plant. The mankind, however, has used secondary metabolite produced by plants since the ancient time. People use plant secondary metabolites as medicine, spices, perfumery, poison, pest control, etc.
Plants have been traditionally used as fungicide for various purposes such as food preservatives and treatment of skin diseases. Tofu that is made from soya curd is rinsed with yellow pigment of turmeric to make the color of tofu into yellow and to extend the shelf life of tofu. Garlic is traditionally used together with cassava starch to catch spore of yeast needed for fermentation of soya bean to make
Many secondary metabolites from plants have been extracted, fractionated, isolated, and studied for the antifungal activity. Volatile oil is the secondary metabolites that play many important roles in human daily life, such as perfumery, spices, essence, medicine, aromatherapy, insect repellent, and also as fungicide [1]. Many medicinal plants contain volatile oil; many of them have been traditionally used in cut healing or as natural preservatives due to their capacity to control the growth of bacteria and or fungi [2]. Coumarin is reported to be one of the antifungal compounds present in the leaves of
2. Plants with antifungal activity
The mankind has been using plants as medicine to treat different kinds of diseases, including fungal infection.
The antifungal plants described above were extracted using methanol, and the extract obtained were tested toward
3. Plant extract antifungal activity on Phytophthora palmivora and Fusarium oxysporum
Most plants reported or traditionally used as antifungi are indeed all active toward
No. | Plant | Plant organ | Concentration | |
---|---|---|---|---|
0.5% | 1.0% | |||
1 | Aerial part | + | ++ | |
2 | Leaves | + | +++ | |
3 | Leaves | ++ | ++ | |
4 | Bulb | ++ | ++ | |
5 | Rhizome | ++ | ++ | |
6 | Rhizome | ++ | +++ | |
7 | Rhizome | +++ | +++ | |
8 | Rhizome | +++ | +++ | |
9 | Rhizome | ++ | ++ | |
10 | Leaves | ++ | ++ | |
11 | Flower bud | ++++ | ++++ |
Table 1.
Note: Extract was made by maceration in methanol: +: 1–25% inhibition; ++: 26–50% inhibition; +++: 51–75% inhibition; ++++: 76–100% inhibition.
Compared to
No. | Plant | Plant organ | Concentration | ||
---|---|---|---|---|---|
2.5% | 5% | 10% | |||
1 | Aerial part | — | — | — | |
2 | Aerial part | — | — | — | |
3 | Leaves | — | — | — | |
4 | Leaves | — | ++ | +++ | |
5 | Leaves | — | — | — | |
6 | Leaves | — | — | — | |
7 | Leaves | — | — | — | |
8 | Leaves | — | + | ++++ | |
9 | Flower bud | +++ | ++++ | ++++ | |
10 | Fruit cortex | — | — | — | |
11 | Bulb | — | — | — | |
12 | Rhizome | — | — | — | |
13 | Rhizome | ++ | ++ | ++ | |
14 | Rhizome | — | — | + | |
15 | Rhizome | — | — | — | |
16 | Rhizome | — | — | + | |
17 | Rhizome | — | ++ | ++ |
Table 2.
Activity of antifungal plant on
Note: Extract was made by maceration in methanol: +: 1–25% inhibition; ++: 26–50% inhibition; +++: 51–75% inhibition; ++++: 76–100% inhibition.
Tables 1 and 2 show that clove bud and clove leaves are potential source of secondary metabolite for antifusarium and antiphytophthora. Clove bud contains 15–20% volatile oil with major components consisting eugenol (80–90%), eugenol acetate (10–15%), and caryophyllene (3%). Clove leaves also contain volatile oil, but the composition is different, and the content is much lower compared to the clove bud. However, the oil content of clove leaf is relatively high compared to the other leaves. The oil content of clove leaves is approximately 2% with the major components which are eugenol 60% and caryophyllene 21
4. The antifungal compounds from Syzygium aromaticum
Clove bud and leaf contain secondary metabolites that strongly inhibit the growth of
Observation under scanning electron microscope showed that the hypha of

Figure 1.
Scanning electron microscopy of normal
Eugenol is suggested to block aromatic and branched chain amino acid synthesis across the cytoplasmic membrane. Eugenol inhibits growth of yeast strain carrying a mutation in gene encoding an enzyme, a tryptophan, phenylalanine, tyrosine, and isoleucine biosynthesis pathway, in a medium supplemented with the related amino acid [44].
There are two approaches to obtain antifusarium from clove. Firstly, the secondary metabolites from clove leaves or buds can be extracted using nonpolar solvent such as hexane, petroleum ether, gasoline, or kerosene. Subsequently, the solvent is removed through evaporation leaving the concentrated extract containing antifusarium and antiphytophthora compounds. Hexane and petroleum ether have relatively low boiling point; therefore, it is easy to evaporate, and while the boiling point of gasoline and kerosene is higher than 100°C, higher temperature or lower pressure is needed to evaporate. By using extraction combined with distillation to recover the solvent, more efficient production system can be developed. Secondly, since eugenol is a component of volatile oil, the oil of clove leaves can be obtained through steam distillation by which the oil will evaporate together with steam, and upon condensation the oil will separate from water and the oil can be collected. To obtain pure eugenol, further separation processes will be needed, such as liquid–liquid extraction, vacuum fraction distillation, and chromatographic techniques.
There are some other plant metabolites having antifungal activity, and the effect is stronger than eugenol. Thymol and other components of volatile oil had been compared, and the results are as shown in Table 3 [45]. Thymol is the component of volatile oil from
Compound | Toxicity index | ||||
---|---|---|---|---|---|
Thymol | 100 | 100 | 100 | 100 | 100 |
Eugenol | 42.2 | 62.02 | 17.23 | 38.14 | 37.77 |
Methyl cinnamate | 49.65 | 57.68 | 16.43 | 28.16 | 81.31 |
Linalool | 11.8 | 11.33 | 4.45 | 6.03 | 0.85 |
1,8-Cineol | 0.0008 | 0.468 | — | — | — |
Table 3.
Relative antifungal activity of plant component compared to thymol.
5. Structure requirement of eugenol derivatives for antifungal activity
Eugenol derivatives had been synthesized and their antifungal activities evaluated [43]. Some structures and their antifungal activities are shown in Figure 2. It seems that the aromatic, ortho-oxygenation, and the double bond at the terminal of side chain are essential for the antifungal activity. The presence of substituents on the hydroxy phenolic reduces the activity. Compound F by which the orthodioxy is connected by a methine bridge becomes inactive (MIC > 250 ppm). The absence of double bond in the side chain eliminates the antifungal activity; this is shown by compound D with MIC >250 ppm and considered to be inactive. If the position of double bond of the side chain is moved to the middle, the antifungal activity also disappears. This is demonstrated by compound H that is inactive. The presence of nitro substituent attached to the aromatic increases antifungal activity, and the nitro at ortho-position to the hydroxy group gives higher activity than at meta-position (compounds B and C).

Figure 2.
Derivatives of eugenol and their antifungal activities.
Base on the above data, the structure requirement for eugenol derivatives to be active as a fungicide is shown in Figure 3.

Figure 3.
The important sites for antifungal activity of eugenol derivatives.
6. Conclusion
Most extracts from plants that have been used as antifungi or reported as antifungi are also active as antiphytophthora but only few of them that are active as antifusarium. Inhibition of
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