Chmielarz Paweł, Kotlarski Szymon, Kalemba Ewa Marzena, Martins João Paulo Rodrigues, Michalak Marcin
Institute of Dendrology Polish Academy of Sciences, Parkowa 5, 62-035 Kórnik, Poland.
PPHU ASKIK Co., Ltd., Bukowy Las 20, 63-014 Murzynowo Kościelne, Poland.
Plants (Basel). 2023 Jun 6;12(12):2230. doi: 10.3390/plants12122230.
The conservation of the genetic resources of old trees is crucial to their ecological role but is extremely difficult, especially for oak species ( spp.) displaying recalcitrance in seed and vegetative propagation methods. Our study aimed to assess the regenerative potential of trees of different ages (up to 800 years) during micropropagation. We also aimed to determine how in vitro conditions can influence in vitro regeneration responses. Lignified branches collected from 67 selected trees were cultivated ex vitro in culture pots at 25 °C to obtain epicormic shoots (explant sources). The explants were cultivated on an agar medium supplemented with 0.8 mg L 6-benzylaminopurine (BAP) for at least 21 months. In a second experiment, two different shoot multiplication conditions (temporary immersion-RITA bioreactor and agar medium) and two culture medium formulations (Woody Plant Medium and modified Quoirin and Lepoivre medium) were tested. The results showed that the mean length of the epicormic shoots obtained in a pot culture was a function of donor age and was similar among the group of younger trees (ca. 20-200 years), and varied between older trees (ca. 300-800 years). The efficiency of in vitro shoot multiplication strictly depended on the genotype. A sustainable in vitro culture (defined as survival after 6 months) was only possible for half of the tested old donor trees, even when they survived the first month of in vitro growth. A continuous monthly increase in the number of in vitro cultured shoots was reported in younger oaks and in some old oaks. We found a significant effect of the culture system and the macro- and micronutrient composition on in vitro shoot growth. This is the first report demonstrating that the in vitro culture can be successfully applied to the propagation of even 800-year-old pedunculate oak trees.
古树遗传资源的保护对其生态作用至关重要,但极具难度,尤其是对于在种子繁殖和营养繁殖方法中表现出顽拗性的栎属树种。我们的研究旨在评估不同树龄(最长达800年)的树木在微繁殖过程中的再生潜力。我们还旨在确定体外培养条件如何影响体外再生反应。从67棵选定的树木上采集木质化枝条,在25℃下于培养盆中进行离体培养,以获得不定芽(外植体来源)。外植体在添加了0.8 mg/L 6 - 苄基腺嘌呤(BAP)的琼脂培养基上培养至少21个月。在第二个实验中,测试了两种不同的芽增殖条件(临时浸没 - RITA生物反应器和琼脂培养基)以及两种培养基配方(木本植物培养基和改良的Quoirin和Lepoivre培养基)。结果表明,盆栽培养中获得的不定芽的平均长度是供体树龄的函数,在较年轻的树组(约20 - 200年)中相似,而在较老的树组(约300 - 800年)中有所不同。体外芽增殖效率严格取决于基因型。即使一半的受试老供体树在体外生长的第一个月存活下来,可持续的体外培养(定义为6个月后存活)也仅对其中一半可行。在较年轻的栎树和一些老栎树中,体外培养芽的数量每月持续增加。我们发现培养系统以及大量和微量营养成分对体外芽生长有显著影响。这是第一份表明体外培养甚至可以成功应用于800年树龄的英国栎树繁殖的报告。