Development of the endosperm of Myrsine laetevirens (Myrsinaceae). I. Cellularization and deposition of cell-wall storage carbohydrates

Myrsine laetevirens has a nuclear type of endosperm development. Vacuole formation in peripheral coenocytic cytoplasm precedes cytokinesis and compartmentalizes the cytoplasm. Cellularization starts as a series of anticlinal walls projecting centripetally. Periclinal cell walls are formed from expan...

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Autor principal: Otegui, M.
Otros Autores: Lima, C., Maldonado, S., De Lederkremer, R.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1999
Acceso en línea:Registro en Scopus
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100 1 |a Otegui, M. 
245 1 0 |a Development of the endosperm of Myrsine laetevirens (Myrsinaceae). I. Cellularization and deposition of cell-wall storage carbohydrates 
260 |c 1999 
270 1 0 |m De Lederkremer, R.M.; Departamento de Quimica Organica, Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, 1428 Buenos Aires, Argentina; email: lederk@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a Myrsine laetevirens has a nuclear type of endosperm development. Vacuole formation in peripheral coenocytic cytoplasm precedes cytokinesis and compartmentalizes the cytoplasm. Cellularization starts as a series of anticlinal walls projecting centripetally. Periclinal cell walls are formed from expanding cell plates following nuclear divisions. The developing walls are flanked by endoplasmic reticulum cisternae with dilated and short profiles and few ribosomes. Subsequent anticlinal wall growth and periclinal divisions elongate the endosperm into the central vacuole, resulting, finally, in the convergence of the advancing tissue. After that, the endosperm increases in size by anticlinal, periclinal, and oblique divisions in all cells of the endosperm and involving phragmoplast and cell plate. Carbohydrate deposition in the cell walls begins 40 d after pollination (DAP) with deposition of pectins in the cell layers next to the embryo. At ca. 50 DAP, the cell walls of the bulk endosperm begin to thicken, showing the presence of xyloglucans. The deposition of new cell-wall material is achieved by the activity of the Golgi stacks located near the cell walls. Neutral sugars were determined after two conditions of acid hydrolysis. Monosaccharides were identified by high-performance anion exchange chromatography (Dionex, Sunnyvale, Calif.). Arabinose, xylose, glucose, and galactose were the main monosaccharides, but their ratio changes during development. Methylation analysis of cell-wall polysaccharides accords with the occurrence of significant amounts of xyloglucans. The presence of pectic polysaccharides can be inferred from the amounts of uronic acids, galactose, arabinose, and rhamnose.  |l eng 
593 |a Laboratorio de Morfologia Vegetal, Facultad de Cie. Naturales y Museo, Universidad Nacional de La Plata, Paseo del Bosque s/n, 1900 la Plata, Argentina 
593 |a Depto. de Quimica Orgánisa, Facultad de Cie. Exact. y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, 1428 Buenos Aires, Argentina 
593 |a Instituto de Recurs. Biologicos, INTA, 1712 Castelar, Argentina 
690 1 0 |a CARBOHYDRATES 
690 1 0 |a ENDOSPERM CELLULARIZATION 
690 1 0 |a ENDOSPERM DEVELOPMENT 
690 1 0 |a MYRSINE LAETEVIRENS 
690 1 0 |a XYLOGLUCANS 
690 1 0 |a MYRSINE LAETEVIRENS 
700 1 |a Lima, C. 
700 1 |a Maldonado, S. 
700 1 |a De Lederkremer, R.M. 
773 0 |d 1999  |g v. 160  |h pp. 491-500  |k n. 3  |p Int. J. Plant Sci.  |x 10585893  |t International Journal of Plant Sciences 
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856 4 0 |u https://doi.org/10.1086/314150  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_10585893_v160_n3_p491_Otegui  |y Handle 
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