Isolation and characterization of cell walls from the mesocarp of mature grape berries (Vitis vinifera)

2020 ◽  
Author(s):  
KJ Nunan ◽  
Ian Sims ◽  
A Bacic ◽  
SP Robinson ◽  
GB Fincher

Cell walls have been isolated from the mesocarp of mature grape (Vitis vinifera L.) berries. Tissue homogenates were suspended in 80% (v/v) ethanol to minimise the loss of water-soluble wall components and wet-sieved on nylon mesh to remove cytoplasmic material. The cell wall fragments retained on the sieve were subsequently treated with buffered phenol at pH 7.0, to inactivate any wall-bound enzymes and to dislodge small amounts of cytoplasmic proteins that adhered to the walls. Finally, the wall preparation was washed with chloroform/methanol (1:1, v/v) to remove lipids and dried by solvent exchange. Scanning electron microscopy showed that the wall preparation was essentially free of vascular tissue and adventitious protein of cytoplasmic origin. Compositional analysis showed that the walls consisted of approximately 90% by weight of polysaccharide and less than 10% protein. The protein component of the walls was shown to be rich in arginine and hydroxyproline residues. Cellulose and polygalacturonans were the major constituents, and each accounted for 30-40% by weight of the polysaccharide component of the walls. Substantial varietal differences were observed in the relative abundance of these two polysaccharides. Xyloglucans constituted approximately 10% of the polysaccharide fraction and the remainder was made up of smaller amounts of mannans, heteroxylans, arabinans and galactans.

2020 ◽  
Author(s):  
KJ Nunan ◽  
Ian Sims ◽  
A Bacic ◽  
SP Robinson ◽  
GB Fincher

Cell walls have been isolated from the mesocarp of mature grape (Vitis vinifera L.) berries. Tissue homogenates were suspended in 80% (v/v) ethanol to minimise the loss of water-soluble wall components and wet-sieved on nylon mesh to remove cytoplasmic material. The cell wall fragments retained on the sieve were subsequently treated with buffered phenol at pH 7.0, to inactivate any wall-bound enzymes and to dislodge small amounts of cytoplasmic proteins that adhered to the walls. Finally, the wall preparation was washed with chloroform/methanol (1:1, v/v) to remove lipids and dried by solvent exchange. Scanning electron microscopy showed that the wall preparation was essentially free of vascular tissue and adventitious protein of cytoplasmic origin. Compositional analysis showed that the walls consisted of approximately 90% by weight of polysaccharide and less than 10% protein. The protein component of the walls was shown to be rich in arginine and hydroxyproline residues. Cellulose and polygalacturonans were the major constituents, and each accounted for 30-40% by weight of the polysaccharide component of the walls. Substantial varietal differences were observed in the relative abundance of these two polysaccharides. Xyloglucans constituted approximately 10% of the polysaccharide fraction and the remainder was made up of smaller amounts of mannans, heteroxylans, arabinans and galactans.


2007 ◽  
Vol 227 (1) ◽  
pp. 223-231 ◽  
Author(s):  
Ana Ortega-Regules ◽  
José María Ros-García ◽  
Ana Belén Bautista-Ortín ◽  
José María López-Roca ◽  
Encarna Gómez-Plaza

2010 ◽  
Vol 45 (6) ◽  
pp. 1243-1249 ◽  
Author(s):  
Ting Zhou ◽  
Quanhong Li ◽  
Jian Zhang ◽  
Haixia Yang ◽  
Guanghua Zhao

2002 ◽  
Vol 127 (6) ◽  
pp. 912-918 ◽  
Author(s):  
Justine E. Vanden Heuvel ◽  
Evangelos D. Leonardos ◽  
John T.A. Proctor ◽  
K. Helen Fisher ◽  
J. Alan Sullivan

Potted `Chardonnay' grapevines (Vitis vinifera L.) with either two or three shoots were grown in a greenhouse for one month and then transferred to a phytotron room, where either one or two shoots were shaded. Twenty-four days after transfer, leaves at the fifth node of either the light-adapted or shade-adapted shoot were exposed to a 2-hour pulse of 14CO2. Both light environment and number of shade shoots on the vine had a significant effect on photosynthate partitioning within the plant following a 22-hour chase. Leaves fed with 14CO2 on a light-adapted shoot translocated 26.1% and 12.7% more radioactivity to the roots and trunk, respectively, than leaves from shade-adapted shoots. Photosynthates were exported from light-adapted leaves to shade-adapted shoots (1.3% of total 14C in plant). The number of shaded shoots and the light environment of the fed leaf had a large effect on partitioning of photosynthates among ethanol-insoluble, water-soluble, and chloroform-soluble fractions within the leaf. Recovered 14C in the water-soluble fraction of the fed leaf appeared to be affected more by number of shoots than by light environment of the fed leaf. The data suggest that there is a sink effect on initial carbon partitioning patterns in grapevine leaves. Sink strength may have a greater role than light environment. A large proportion of interior leaves versus exterior leaves may be costly with respect to the carbohydrate budget of a vine.


Planta ◽  
1997 ◽  
Vol 203 (1) ◽  
pp. 93-100 ◽  
Author(s):  
Kylie J. Nunan ◽  
Ian M. Sims ◽  
Antony Bacic ◽  
Simon P. Robinson ◽  
Geoffrey B. Fincher

Planta ◽  
1997 ◽  
Vol 203 (1) ◽  
pp. 93-100 ◽  
Author(s):  
Kylie J. Nunan ◽  
Ian M. Sims ◽  
Antony Bacic ◽  
Simon P. Robinson ◽  
Geoffrey B. Fincher

2011 ◽  
Vol 6 (2) ◽  
pp. 216-222
Author(s):  
Lucia Andreini ◽  
Raffaella Viti ◽  
Giancarlo Scalabrelli

AbstractEsca is a destructive disease of the woody tissues of grapevine (Vitis vinifera L.) and due to the complexity of disease many aspects of host-pathogen interactions are not clearly understood. The histological characteristics of esca symptomatic petioles and internodes, collected from Cabernet Sauvignon and Sangiovese grapevine were studied. The tissues were fixed in FAA, dehydrated and embedded in Histoplast. To identify the lignified cell walls the sections were stained by Crystal violet and Erythrosin B and observed using an optical microscope. The main feature of tissues infected by esca disease was the minor lignification of vascular tissues, which was observed in petiole tissues before appearance of esca symptoms. The opportunity to utilize the histological examination of tissues as a method for the early detection of esca infections is hypothesized for the future application.


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