<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">El Kbiach, M L</style></author><author><style face="normal" font="default" size="100%">Lamarti, A</style></author><author><style face="normal" font="default" size="100%">Abdali, A</style></author><author><style face="normal" font="default" size="100%">Badoc, A</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Micropropagation of cork oak (Quercus suber L.) by apical bud culture from embryonic axes</style></title><secondary-title><style face="normal" font="default" size="100%">ACTA BOTANICA GALLICA</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Cork oak</style></keyword><keyword><style  face="normal" font="default" size="100%">embryon</style></keyword><keyword><style  face="normal" font="default" size="100%">in vitro culture</style></keyword><keyword><style  face="normal" font="default" size="100%">Quercus suber</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2004</style></year></dates><publisher><style face="normal" font="default" size="100%">SOC BOTANIQUE FRANCE</style></publisher><pub-location><style face="normal" font="default" size="100%">FACULTE DE PHARMACIE, BP 83, F-59006 LILLE-CEDEX, FRANCE</style></pub-location><volume><style face="normal" font="default" size="100%">151</style></volume><pages><style face="normal" font="default" size="100%">401-413</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">To improve the in vitro germination and development of cork Oak&lt;br/&gt;embryonic axes, several mineral media were tested; Durzan medium&lt;br/&gt;modified 1/2 supplemented with 400 mg/l glutamine and 3% sucrose gave&lt;br/&gt;the best results. The action of BA alone or combined with other growth&lt;br/&gt;regulators was also studied. A low concentration (0.44 mu M) was found&lt;br/&gt;to give an acceptable percentage of plantlets. When combined with NAA,&lt;br/&gt;callogenesis was observed. The transfer of cultures in conditions of low&lt;br/&gt;luminosity led to the formation of several axillary buds. These buds&lt;br/&gt;were multiplied on a solid medium supplemented with GA(3) at low&lt;br/&gt;concentration. The buds were elongated, then rooted on a growth&lt;br/&gt;regulator-free medium after brief dipping in an auxinic solution. The&lt;br/&gt;rooted plants were potted on horticultural substrate.</style></abstract></record></records></xml>