Abstract
Analysis of stem extracts identified large quantities of 3,4-dihydroxybenzoic acid and other similar phenolics. The exogenous application of 3,4-dihydroxybenzoic acid on Protea cynaroides explants in vitro significantly increased the root mass at 100 mg l−1, but not at lower concentrations, while root inhibition was observed at 500 mg l−1. HPLC analysis of cuttings during vegetative propagation showed a considerable increase in 3,4-dihydroxybenzoic acid levels from initial planting to when root formation took place, indicating for the first time that 3,4-dihydroxybenzoic acid may be an important phenolic compound in regulating root formation in P. cynaroides cuttings. HPLC analysis also identified caffeic, ferulic, gallic and salicylic acids in the cuttings.
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An M, Haig T, Pratley JE (2000) Phytotoxicity of Vulpia residues: II. Separation, identification, and quantification of allelochemicals from Vulpia myuros. J Chem Ecol 26(6):1465–1476
Bär W, Pfeifer P, Dettner K (1997) Intra- and inter-specific Allelochemical effects in three Kalanchoe-species (Crassulaceae). J Biosciences 52(7–8):441–449
Belz RG, Reinhardt CF, Foxcroft LC, Hurle K (2007) Residue allelopathy in Parthenium hysterophorus L. – does parthenin have a leading part? Crop Protection 26(3):237–245
Biran I, Halevy AH (1973) Endogenous levels of growth regulators and their relationship to the rooting of dahlia cuttings. Physiol Plant 28:244–247
Bothma A (2002) Allelopathic potential of silverleaf nightshade. (Solanum elaeagnifolium Cav.). MSc Thesis. Department of Plant Production and Soil Science, University of Pretoria, Pretoria, South Africa
Chou C-H, Hwang S-Y, Peng C-I (1987) The selective allelopathic interaction of a pasture-forest intercropping in Taiwan. Plant Soil 98:31–41
Chou C-H, Muller CH (1972) Allelopathic mechanisms of Arctostaphylos glandulosa var. zacaensis. Am Midl Nat 88(2):324–347
Debergh PJ, Read PJ (1991) Micropropagation. In: Debergh PC, Zimmerman RH (eds) Micropropagation: Technology and application. Dordrecht Kluwer Academic Publishers, pp 1–14
Dhawan RS, Nanda KK (1982) Stimulation of root formation on Impatiens balsamina L. cuttings by coumarin and the associated biochemical changes. Biologia Plant 24(3):177–182
Einhellig FA (2004) Mode of allelochemical action of phenolic compounds. In: Macías FA, Galindo JCG, Molinillo JMG, Cutler HG (eds) Allelopathy: Chemistry and mode of action of allelochemicals. CRC Press
Elzaawely AA, Xuan TD, Tawata S (2005) Allelopathic activity and identification of allelochemicals from Rumex japonicus Houtt. Allelopathy J 16(2):209–216
Fadl MS, Hartmann HT (1967) Relationship between seasonal changes in endogenous promoter and inhibitors in pear buds and cutting bases and the rooting of pear hardwood cuttings. Proc Am Soc Hort Sci 91:96–112
George EF (1996) Plant propagation by tissue culture. Part 2: In Practice, 2nd edn. Exegetics Ltd. Edington, Wilts. BA13 4QG, England, pp 639–651
Hackett WP (1970) The influence of auxin, catechol and methanolic tissue extracts on root initiation in aseptically cultured shoot apices of the juvenile and adult forms of Hedera helix. J Am Soc Hort Sci 95:398–402
Hammerschlag F (1982) Factors influencing in vitro multiplication and rooting of the plum rootstock ‘Myrobalan’ (Prunus cerasifera Ehrh.). Journal of the American Society for Horticultural Science 107:44–47
James DJ, Thurbon IJ (1981) Shoot and root initiation in vitro in the apple rootstock M9 and the promotive effects of phloroglucinol. J Hort Sci 56:15–20
Jones OP, Hatfield SGS (1976) Root initiation in apple shoots cultured in vitro with auxins and phenolic compounds. J Hort Sci 51:495–499
Kil B-S, Lee SY (1987) Allelopathic effects of Chyrsanthemum morifolium on germination and growth of several herbaceous plants. J Chem Ecol 13(2):299–308
Kim YO, Johnson JD, Lee EJ (2005) Phytotoxicity effects and chemical analysis of leaf extracts from three Phytolaccaceae species in South Korea. J Chem Ecol 31(5):1175–1186
Kling GJ, Meyer MM Jr (1983) Effects of phenolic compounds and indoleacetic acid on adventitious root initiation in cuttings of Phaseolus aureus, Acer saccharinum, and Acer griseum. HortScience 18(3):352–354
Liu DL, An M, Johnson IR, Lovett JV (2003) Mathematical modelling of allelopathy. III. A model for curve-fitting allelochemical dose responses. Nonlinearity Biol Toxicol Med 1(1):37–50
Masterton WL, Slowinski EJ, Stanitski CL (1987) Chemical principles. 6th edn. Holt-Saunders International, pp 360–364
Morsink WAG, Smith VG (1975) The effect of some monohydrobenzoic and dihydrobenzoic acids as auxin synergists on rooting softwood cuttings of basswood (Tilia americana) under mist. Can J Forest Res 5:500–502
Mucciarelli M, Scannerini S, Gallino M, Maffei M (2000) Effects of 3,4-dihydroxybenzoic acid on tobacco (Nicotiana tabacum L.) cultured in vitro. Growth regulation in callus and organ cultures. Plant Biosyst 134(2):185–192
Murashige T, Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiol Plant 15:473–497
Pellissier F (1994) Effect of phenolic compounds in humus on the natural regeneration of spruce. Phytochemistry 36(4):865–867
Perold WG, Beylis P, Howard AS (1973) Metabolites of Proteaceae. Part VII. The occurrence of (+)-d-allose in nature: Rubropilosin and pilorubrosin from Protea rubropilosa Beard. J Chem Soc Perkin Trans I:643–649
Reuveni O, Adato I (1974) Endogenous carbohydrates, root promoters and root inhibitors in easy- and difficult-to-root date palm. (Phoenix dactylifera L.) offshoots. J Am Soc Hort Sci 99:361–363
Rice EL (1984) Allelopathy. Academic Press, Orlando, pp 272–274
Richards M (1964) Root formation on cuttings of Camellia reticulate var. ‘Capt. Rawes’. Nature 204:601–602
San Antonio JP (1952) The role of coumarin in the growth of roots of Melilotus alba. Bot Gaz 114:79–95
Sang S, Lapsley K, Jeong W-S, Lachance PA, Ho C-T, Rosen RT (2002) Antioxidative phenolic compounds islated from almond skins (Prunus amygdalus Batsch). J Agric Food Chem 50:2459—2463
SAS Institute Inc (1996) The SAS system for Windows. SAS Institute Inc. SAS Campus drive, Cary, North Carolina, USA
Still SM, Dirr MA, Gartner JB (1976) Phytotoxic effects of several bark extracts on mung bean and cucumber growth. J Am Soc Hort Sci 101:34–37
Taylor GG, Odom RE (1970) Some biochemical compounds associated with rooting of Carya illinoensis stem cuttings. J Am Soc Hort Sci 95:146–151
Verotta L, Orsini F, Pelizzoni F, Torri G, Rogers CB (1999) Polyphenolic glycosides from African Proteacae. J Nat Prod 62:1526–1531
Wu HC (2006) Improving in vitro propagation of Protea cynaroides L. (King Protea) and the roles of starch and phenolic compounds in the rooting of cuttings. PhD thesis. University of Pretoria, Pretoria
Wu HC, Du Toit ES, Reinhardt CF (2007) Micrografting of Protea cynaroides. Plant Cell Tiss Org Cult 89(1):23–28
Zhiqun H, Haig T, Silong W, Sijie H (2002) Autotoxicity of Chinese fir on seed germination and seedling growth. Allelopathy J 9(2):187–193
Zimmerman RH (1984) Rooting apple cultivars in vitro: Interactions among light, temperature, phloroglucinol and auxin. Plant Cell Tiss Org Cult 3:301–311
Acknowledgements
The authors are indebted to Dr. S. O. Duke for his invaluable advice and discussions during this research. The authors also thank Dr. Gordon Bredenkamp for providing the plant materials.
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Wu, H.C., du Toit, E.S., Reinhardt, C.F. et al. The phenolic, 3,4-dihydroxybenzoic acid, is an endogenous regulator of rooting in Protea cynaroides . Plant Growth Regul 52, 207–215 (2007). https://doi.org/10.1007/s10725-007-9191-1
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DOI: https://doi.org/10.1007/s10725-007-9191-1