Abstract
Chlorogenic acid (CGA) and rutin in various concentrations and application times were examined over a period of three years to determine their effectiveness in adventitious rooting on the leafy cuttings of an easy to root olive cultivar, ‘Arbequina’ and a recalcitrant one ‘Kalamata’. Exogenous application of phenolics and the season the cuttings were collected affected significantly the rooting potential of both cultivars. The rooting efficiency of ‘Arbequina’ treated with IBA alone was 51% in summer and 90% in autumn. Among the phenolics, in ‘Arbequina’, the highest rooting was recorded after the application of 0.1 mM CGA for 30 min reaching 88% in summer (37% increase) and 100% in autumn (10% increase). In ‘Kalamata’, IBA was almost ineffective in both seasons, as was also the case for the applied phenolics in summer. The greatest overall rooting, for ‘Kalamata’ (25%) occurred in autumn, when the cuttings’ bases were immersed with 0.1 mM CGA for 30 min, corresponding nearly to 830% increase in the rooting performance compared to control. Carbohydrate concentration was also assessed in ‘Kalamata’ cuttings to examine the influence of CGA in adventitious rooting. It was found that glucose and starch concentration increased during rhizogenesis, whereas the other soluble sugars, except for fructose, exhibited high concentrations at day 1 and 7. The ratio of hexoses/starch, sucrose/starch and sucrose/hexoses exhibited lower values in CGA treated cuttings compared to control. Thus, CGA enhanced rooting performance in both olive cultivars, possibly through a modification of carbohydrate’s ratios, strengthening therefore their role in rhizogenesis.
Similar content being viewed by others
Abbreviations
- CGA:
-
Chlorogenic acid
- cv:
-
Cultivar
- DAP:
-
Days after planting
- DW:
-
Dry weight
- EPR:
-
Early phases of rhizogenesis
- IAA:
-
Indole-3-acetic acid
- IBA:
-
Indole-3-butyric acid
References
Agulló-Antón MÁ, Ferrández-Ayela A, Fernández-García N, Nicolás C, Albacete A, Pérez-Alfocea F, Sánchez-Bravo J, Pérez-Pérez JM, Acosta M (2014) Early steps of adventitious rooting: morphology, hormonal profiling and carbohydrate turnover in carnation stem cuttings. Physiol Plant 150(3):446–462. https://doi.org/10.1111/ppl.12114
Bahmani R, Karmai O, Gholami M (2009) Influence of carbon sources and their concentration on rooting and hyperhydricity of apple rootstock MM. 106. Word Appl Sci J 6(11):1513–1517
Basak UC, Das AB, Das P (1995) Metabolic changes during rooting in stem cuttings of five mangrove species. Plant Growth Regul 17:141–148. https://doi.org/10.1007/BF00024174
Costa JM, Heuvelink E, Van de Pol PA, Put HMC (2007) Anatomy and morphology of rooting in leafy rose stem cuttings and starch dynamics following severance. Acta Hortic 751:495–502. https://doi.org/10.17660/ActaHortic.2007.751.63
Couvillon GA (1988) Rooting responses to different treatments. Acta Hortic 227.
Cristofori V, Rouphael Y, Rugini E (2010) Collection time, cutting age, IBA and putrescine effects on root formation in Corylus avellana L. cuttings. Sci Hortic 124:189–194. https://doi.org/10.1016/j.scienta.2009.12.034
Curir P, Sulis S, Mariani F, van Sumere CF, Marchesini A, Dolci M (1993) Influence of endogenous phenols on rootability of Chamaelaucium uncinatum Schauer stem cuttings. Sci Hortic 55:103–314
Davies PJ (2004) The plant hormones: their nature, occurrence and functions. In: Davies PJ (ed) Plant hormones: biosynthesis, signal transduction, action, 3rd edn. Kluwer Academic Publishers, Dordrecht, pp 1–15
Del Rio C, Rallo L, Caballero JM (1991) Effects of carbohydrate content on the seasonal rooting of vegetative and reproductive cuttings of olive. J Hortic Sci 66:301–309. https://doi.org/10.1080/00221589.1991.11516157
Denaxa N-K, Vemmos SN, Roussos PA (2012) The role of endogenous carbohydrates and seasonal variation in rooting ability of cuttings of an easy and a hard to root olive cultivars (Olea europaea L.). Sci Hortic 143:19–28. https://doi.org/10.1016/j.scienta.2012.05.026
Denaxa N-K, Roussos PA, Vemmos SN, Fasseas K (2019) Assessing the effect of oxidative enzymes and stem anatomy on adventitious rooting of Olea europaea (L.) leafy cuttings. Span J Agric Res 17(3):e0803
Doud S, Carlson R (1977) Effects of etiolation, stem anatomy and starch reserves on root initiation of layered Mallus clones. J Amer Soc Hortic Sci 102:487–491
Fabbri A, Bartolini G, Lambardi M, Kailis SG (2004) Olive propagation manual. Landlinks Press, Collingwood
Fontanazza G (1993) Olivicoltura intensiva meccanizzata, Edagricole. Italy, Bologna, p 103
Friend AL, Coleman MD, Isebrands JG (1994) Carbon allocation to root and shoot systems of woody plants. In: Davis TD, Haissig BE (eds) Biology of adventitious root formation. Plenum Press, New York, pp 245–273
Gaspar T, Kevers C, Hausman JF (1997) Indissociable chief factors in the inductive phase of adventitious rooting. In: Altman A, Waisel Y (eds) Biology of root formation and development. Plenum Press, New York, pp 55–63
Gaspar T, Kevers C, Penel C, Greppin H, Reid DM, Thorpe TA (1996) Plant hormones and plant growth regulators in plant tissue culture. Vitro Cell Dev Biol Plant 32:272–289. https://doi.org/10.1007/BF02822700
Haissig BE (1984) Carbohydrate accumulation and partitioning in Pinus banksiana seedlings and seedling cuttings. Physiol Plant 61:13–19
Haissig BE (1989) Carbohydrate relations during propagation of cuttings from sexually mature Pinus banksiana trees. Tree Physiol 5:319–328
Haissig BE (1990) Reduced irradiance and applied auxin influence carbohydrate relations in Pinus banksiana cuttings during propagation. Physiol Plant 78:455–461. https://doi.org/10.1111/j.1399-3054.1990.tb09063.x
Hammerschlag FA, Bauchan GR, Scorza R (1987) Factors influencing in vitromultiplication and rooting of peach cultivars. Plant Cell Tissue Organ Cult 8(3):235–242. https://doi.org/10.1007/BF00040950
Hartmann HT, Kester DE, Davies FT, Geneve RL (2002) Plant propagation principles and practices, 7th edn. Prentice-Hall, New Jersey
Husen A, Pal M (2007) Metabolic changes during adventitious root primordium development in Tectona grandis Linn. F. (teak) cuttings as affected by age of donor plants and auxin (IBA and NAA) treatment. New For 33:309–323. https://doi.org/10.1007/s11056-006-9030-7
Jasik J, De Klerk GJ (1997) Anatomical and ultrastructural examination of adventitious root formation in stem slices of apple. Biol Plant 39:79–90. https://doi.org/10.1023/A:1000313207486
Lavee S, Avidan N, Pierik RLM (1994) Chlorogenic acid—an independent morphogenesis regulator or a cofactor. Acta Hortic 381:405–412
Li M, Leung DWM (2000) Starch accumulation is associated with adventitious root formation in hypocotyl cuttings of Pinus radiata. Plant Growth Regul 19:423–428. https://doi.org/10.1007/s003440000020
Muller B, Stosser M, Tardieu F (1998) Spatial distributions of tissue expansion and cell division rates are related to irradiance and to sugar content in the growing zone of maize roots. Plant Cell Environ 21:149–158. https://doi.org/10.1046/j.1365-3040.1998.00263.x
Osterc G, Štefančič M, Solar A, Štampar F (2007) Potential involvement of flavonoids in the rooting response of chestnut hybrid (Castanea crenata x Castanea sativa) clones. Aust J Expl Agric 47:96–102
Osterc G, Štefančič M, Solar A, Štampar F (2008) Phenolic content in cuttings of two clones of hybrid chestnut (Castanea crenata x Castanea sativa) in the first days after cutting severance. Acta Agric Scand B 58:162–168. https://doi.org/10.1080/09064710701464719
Ozkaya MT, Celik M (1999) Qualitative analysis of phenolic compounds in olive cuttings. Acta Hort 474:477–480
Rabin RS, Klein RM (1957) Chlorogenic acid as a competitive inhibitor of indoleacetic acid oxidase. Arch Biochem Biophys 70:11–15
Rathore JS, Rai MK, Phulwaria M, Shekhawat NS (2014) A liquid culture system for improved micropropagation of mature Acacia nilotica (L.) Del. ssp. indica and ex vitro rooting. Proc Natl Acad Sci India Sect B 84:193–200. https://doi.org/10.1007/s40011-013-0204-8
Reddy KVR, Reddy P, Goud PV (2008) Role of auxins synergists in the rooting hardwood and semi hardwood cuttings of fig (Ficus carica L.). Indian J Agric Res 42(1):47–51
Sebastiani L, Tognetti R (2004) Growing season and hydrogen peroxide effects on root induction and development Olea europaea L. (cvs ‘Frantoio’ and ‘Gentile di Larino’) cuttings. Sci Hortic 100:75–82. https://doi.org/10.1016/j.scienta.2003.08.008
Sturm A, Tang G-Q (1999) The sucrose-cleaving enzymes of plants are crucial for development, growth and carbon partitioning. Trends Plant Sci 4(10):401–407. https://doi.org/10.1016/S1360-1385(99)01470-3
Toledo MEA, Ueda Y, Imahori Y, Ayaki M (2003) L-ascorbic acid metabolism in spinach (Spinacia oleracea L.) during postharvest storage in light and dark. Postharvest Biol Technol 28:47–57. https://doi.org/10.1016/S0925-5214(02)00121-7
Trobec M, Štampar F, Veberič R, Osterc G (2005) Fluctuations of different endogenous phenolic compounds and cinnamic acid in the first days of the rooting process of cherry rootstock ‘GiSelA 5’ leafy cuttings. J Plant Physiol 162:589–597. https://doi.org/10.1016/j.jplph.2004.10.009
Veierskov B (1989) Relations between carbohydrates and adventitious root formation. In: Davis TD, Haissig BE, Sankhla N (eds) Adventitious root formation in cuttings. Dioscorides Press, Portland, pp 70–78
Vemmos SN (1999) Carbohydrate content of inflorescent buds of defruited and fruiting pistachio (Pistachia vera L) branches in relation to biennal bearing. J Hortic Sci Biotech 74:94–100. https://doi.org/10.1080/14620316.1999.11511079
Weschke W, Panitz R, Gubatz S, Wangy Q, Radchuk R, Weber H, Wobus UB (2003) The role of invertases and hexose transporters in controlling sugar ratios in maternal and filial tissues of barley caryopses during early development. Plant J 33:395–411. https://doi.org/10.1046/j.1365-313x.2003.01633.x
Wiesman Z, Lavee S (1995) Enhancement of stimulatory effects on rooting of olive cultivar stem cuttings. Sci Hortic 62:189–198. https://doi.org/10.1016/0304-4238(95)00772-L
Yoo YK, Kim KS (1996) Seasonal variation in rooting ability, plant hormones, carbohydrate, nitrogen, starch and soluble sugar contents in cuttings of White Forsythia (Abeliophyllum distichum Nakai). J Kor Soc Hortic Sci 37(4):554–560
Funding
The authors received no specific funding for this work.
Author information
Authors and Affiliations
Contributions
Conceived and designed the experiments: RP, VS and DN-K. Performed the experiments and analyzed the data: DN-K and KDG. Contributed reagents and materials: KDG, VS and RP. Supervising the experiment: VS and RP. RP. The first draft of the manuscript was written by DN-K and the revision of the manuscript was made by RP. All authors read and approved the final manuscript to be published.
Corresponding author
Ethics declarations
Conflict of interest
On behalf of all authors, the corresponding author states that there is no conflict of interest.
Availability of Data and Material
On behalf of all authors, the corresponding author states that all data and material are available.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Denaxa, NK., Petros, R.A., Georgios, K.D. et al. Chlorogenic Acid: A Possible Cofactor in the Rooting of ‘Kalamata’ Olive Cultivar. J Plant Growth Regul 40, 2017–2027 (2021). https://doi.org/10.1007/s00344-020-10249-3
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00344-020-10249-3