Annals of Botany 83: 619-629, 1999
© 1999 Annals of Botany Company
Anatomical and Biochemical Events duringin vitroRooting of Microcuttings from Juvenile and Mature Phases of Chestnut
Instituto de Investigaciones Agrobiológicas de Galicia, CSIC, Apartado 122, 15080, Santiago de Compostela, Spain Escuela Politécnica Superior, Departamento de Producción Vegetal, Polígono de Fingoy, 27002, Lugo, Spain
June 11, 1998 ; September 16, 1998 . February 13, 1999
A comparative study of thein vitrorooting process of chestnut (Castanea sativa)shoots of the same genotype exhibiting juvenile (easy-to-root) and mature (difficult-to-root) characteristics is described. The two culture lines originated from shoots collected from the base (juvenile) and crown (mature) of an 80-year-old tree. Anatomically, juvenile and mature shoots had a similar stem structure at the time of excision, the main difference being that secondary phloem and xylem were more developed in mature than in juvenile shoots. A substantial reactivation of cell division was observed in both shoot lines 48 h after the root inductive treatment with indole-3-butyric acid. Meristemoids and root primordia developed only in juvenile shoots, beginning 3 d after the inductive treatment, and the first adventitious roots emerged 10 d after treatment. However, in mature shoots periclinal divisions of cambial cells occurred, especially on the phloem side, maintaining the normal orientation of the cambial derivatives. No meristemoids formed in this proliferating tissue. During the time course of the rooting process, more endogenous indole-3-acetic acid (IAA) was detected in mature than in juvenile shoots, indicating that the level of IAA is not the limiting factor accounting for the lack of rooting capacity in mature shoots. The levels of polyamines (putrescine, spermine and spermidine) were also higher in mature than in juvenile shoots.Copyright 1999 Annals of Botany Company
Adventitious rooting, anatomy, auxins,Castanea sativaMill., chestnut, juvenile phase, mature phase, polyamines, tissue culture.
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