Arras G, Pani G, Molinu M G, Dore A, Venditti T, Petretto A, Marceddu S, D'Hallewin G
C.N.R.- Istituto di Scienze delle Produzioni Alimentari Traversa la Crucca, 3 - Loc. Baldinca - 07040 Sassari, Italy.
Commun Agric Appl Biol Sci. 2010;75(4):555-62.
The activity of 2-deoxy-D-gLucose (2-DG) alone or in combination with a biocontrol yeast (Candida saitoana, strain 8C) was evaluated in vitro and in vivo against citrus green mould (Penicillium digitatum Sacc.). The in vitro assays were performed on amended potato dextrose agar (PDA) containing 0, 1.5, 3.0, 6.0, 15.0, 30.0 or 60.0 mM of 2-DG. P. digitatum conidia were sown on the amended media and growth inhibition occurred starting from 6.0 mM. A nearly total inhibition of the growth and spore germination occurred with 60.0 mM of 2-DG. The antagonist was not affected by any of the 2-DG concentrations employed and the amended plates resulted well colonized within 2 d post-treatment. In vivo assays were carried out with 'Hamlin' oranges, inoculated with P. digitatum 24 h before treating with: the antagonist; the above reported concentrations of 2-DG, or by combining the two treatments. Seven days post-treatment the inhibition activity exerted by 3.0, 6.0, 15.0, 30.0 and 60.0 mM of 2-DG combined with the yeast was 15, 37, 42, 63 and 84%, respectively. While that exerted by the antagonist was 22% and that by the different concentrations of 2-DG were 7, 11, 27, 42 and 57%, respectively. Compared to single treatments, the co-application significantly and in a synergic mode improved the control of decay. Alterations to the hyphae were observed by SEM when the pathogen was cultured on amended media and into the wounds of inoculated oranges.
单独或与生物防治酵母(斋藤假丝酵母8C菌株)联合使用2-脱氧-D-葡萄糖(2-DG),在体外和体内对柑橘绿霉(指状青霉萨卡多)进行了活性评估。体外试验在添加了0、1.5、3.0、6.0、15.0、30.0或60.0 mM 2-DG的改良马铃薯葡萄糖琼脂(PDA)上进行。将指状青霉分生孢子接种在改良培养基上,从6.0 mM开始出现生长抑制。60.0 mM的2-DG对生长和孢子萌发几乎完全抑制。拮抗剂不受所用任何2-DG浓度的影响,处理后2天内改良平板上就有良好的定殖。体内试验用‘哈姆林’橙子进行,在处理前24小时接种指状青霉,处理方式如下:单独使用拮抗剂;上述浓度的2-DG;或两种处理联合使用。处理7天后,3.0、6.0、15.0、30.0和60.0 mM的2-DG与酵母联合使用的抑制活性分别为15%、37%、42%、63%和84%。单独使用拮抗剂的抑制活性为22%,不同浓度2-DG的抑制活性分别为7%、11%、27%、42%和57%。与单一处理相比,联合应用以协同方式显著提高了对腐烂的控制效果。当病原体在改良培养基上培养以及在接种橙子的伤口中培养时,通过扫描电子显微镜观察到了菌丝的变化。