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P-93<br />

Development of table <strong>and</strong> raisin grapes <strong>with</strong> high anthocyanins using a leaf disk assay<br />

D.W. Ramming* 1 <strong>and</strong> P. Cousins 2<br />

1 USDA-ARS San Joaquin Valley Agricultural Sciences Center, Parlier, California, USA;<br />

2 USDA-ARS Grape Genetics Research Unit, NYS Agric. Expt. Station, Geneva, New York,<br />

USA<br />

*Corresponding author: david.ramming@ars.usda.gov<br />

Anthocyanins are considered an excellent source of antioxidant phytochemicals for health<br />

benefits. The majority of wine, table <strong>and</strong> raisin grapes have anthocyanins only in their colored<br />

skin. Anthocyanin content of grapes would be increased if their flesh also contained<br />

anthocyanins. The ‘Rubired’ wine grape has black skin <strong>and</strong> red fleshed berries. It was used as a<br />

pollen parent to introgress red flesh in a cross <strong>with</strong> a seedless female flowered table grape<br />

selection C33-30. It has red skin <strong>and</strong> white flesh berries. The F1 progeny segregated in a 3<br />

colored:1 white skin <strong>and</strong> 1 red:1 clear flesh ratio for colored berries. Seedlings expressing the<br />

highest level of anthocyanins in the flesh <strong>and</strong> skin were equivalent to ‘Rubired’. Seven modified<br />

backcross families were created by crossing red flesh seeded F1 selections <strong>with</strong> seedless red skin<br />

table or white skin raisin grapes. Skin color segregated as a single dominant gene as expected.<br />

One red flesh parent was heterozygous for skin color <strong>and</strong> the rest were homozygous. Only<br />

seedlings <strong>with</strong> colored skin had red flesh. Flesh color segregated as a 1 red:1 clear in three of the<br />

families or in a 2:1 ratio indicting either a single dominant gene or several genes, <strong>with</strong> red flesh<br />

being predominant. One red flesh parent produced an abnormally high percentage (>80%) of red<br />

flesh seedlings. The assay consisted of placing leaf disks in 10% sucrose solution <strong>and</strong> observing<br />

the development of anthocyanins after 5-10 days under 12 hr photoperiod at 26C. When no<br />

anthocyanin developed in the leaf disks, their seedlings had clear flesh <strong>with</strong> white, red or black<br />

skin (30% of population) <strong>and</strong> could be discarded <strong>with</strong> confidence. Red skin seedlings <strong>with</strong> light<br />

red to red flesh as well as black skin <strong>with</strong> dark red flesh were identified accurately (>50% red in<br />

leaf disk). In some cases seedlings <strong>with</strong> red or black skin <strong>and</strong> clear flesh produced anthocyanins<br />

in the leaf disks <strong>and</strong> were not easily differentiated from black skin <strong>with</strong> light red or red flesh.<br />

174


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