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Review
. 2010 Dec 7;15(12):8933-52.
doi: 10.3390/molecules15128933.

Phenolics and plant allelopathy

Affiliations
Review

Phenolics and plant allelopathy

Zhao-Hui Li et al. Molecules. .

Abstract

Phenolic compounds arise from the shikimic and acetic acid (polyketide) metabolic pathways in plants. They are but one category of the many secondary metabolites implicated in plant allelopathy. Phenolic allelochemicals have been observed in both natural and managed ecosystems, where they cause a number of ecological and economic problems, such as declines in crop yield due to soil sickness, regeneration failure of natural forests, and replanting problems in orchards. Phenolic allelochemical structures and modes of action are diverse and may offer potential lead compounds for the development of future herbicides or pesticides. This article reviews allelopathic effects, analysis methods, and allelopathic mechanisms underlying the activity of plant phenolic compounds. Additionally, the currently debated topic in plant allelopathy of whether catechin and 8-hydroxyquinoline play an important role in Centaurea maculata and Centaurea diffusa invasion success is discussed. Overall, the main purpose of this review is to highlight the allelopacthic potential of phenolic compounds to provide us with methods to solve various ecology problems, especially in regard to the sustainable development of agriculture, forestry, nature resources and environment conservation.

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Figures

Figure 1
Figure 1
Biosynthetic pathways of major allelopathic substances [9].
Figure 2
Figure 2
Main phenolic allelochemicals isolated from aqueous extracts of D. regia [15].
Figure 3
Figure 3
Three phenolic allelochemicals isolated from A. conyzoides rhizosphere soil [21].
Figure 4
Figure 4
Four phenolic allelochemicals isolated from Eucalyptus [23].
Figure 5
Figure 5
Two phenolic allelochemicals for cucumber bioassays [37].
Figure 6
Figure 6
Coumarin for lettuce bioassays [39].
Figure 7
Figure 7
Structures of tannic acid for plant enzyme-activities bioassays [42].
Figure 8
Figure 8
Mechanism of allelochemicals [9].
Figure 9
Figure 9
Structures of both enantiomers of catechin in C. maculosa root exudates [54].
Figure 10
Figure 10
Structure of8-hydroxyquinoline isolated from C. diffusa root exudates.
Figure 11
Figure 11
Some puative allelochemicals isolated from aqueous extract of P. schrenkiana litters.

References

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