Ueta Ikuo, Masuda Suguru, Kataoka Ryota
Department of Applied Chemistry, University of Yamanashi, 4-3-11 Takeda, Kofu, 400-8511, Japan.
Faculty of Life and Environmental Sciences, University of Yamanashi, Kofu, 400-0085, Japan.
Anal Sci. 2025 Jul;41(7):1097-1101. doi: 10.1007/s44211-025-00783-z. Epub 2025 Apr 30.
This study proposes a method for the extraction of volatile organic compounds (VOCs) generated by Trichoderma species and plant endophytic fungi. In this method, generated VOCs are extracted using a needle-type extraction device and analyzed using gas chromatography-mass spectrometry. To extract VOCs generated by a single cultured fungi species, each fungi species was cultivated in a sealed 100 mL polypropylene bottle. Before cultivation, two silicone septa were attached to the bottle and cap. After the preparation of the culture media in the bottle, the bottle was autoclaved and the fungi were inoculated. The bottle was then sealed with a cap, and the air in the bottle was replaced with clean air. The surfaces of the extraction needle and a gas supply needle were sterilized with ethanol and inserted into the bottle via the two silicone septa. A gas sampling bag filled with pure air was connected to the gas supply needle, and clean air was continuously supplied to the bottle as the purge gas during the gas sampling. As the extraction needle, a double-bed-type adsorbent, Carbopack-X and a carbon molecular sieve, was used 3-Methyl butanol and 2-methyl butanol were detected for 41 species, and 2-pentylfran and 6-pentyl-2-pyrone were detected for 2 species among the 46 considered Trichoderma species. Monoterpenes and sesquiterpenes were detected for a single plant endophytic fungus species. The limit of detection of standard 3-methyl butanol and 2-methyl butanol in the proposed method was 0.5 ng mL. The performance of the proposed method was compared with that of the commercial MonoTrap method.
本研究提出了一种提取木霉菌和植物内生真菌产生的挥发性有机化合物(VOCs)的方法。在该方法中,使用针式提取装置提取产生的VOCs,并采用气相色谱-质谱联用仪进行分析。为了提取单一培养真菌物种产生的VOCs,将每种真菌物种在一个密封的100 mL聚丙烯瓶中培养。培养前,在瓶子和瓶盖上粘贴两个硅橡胶隔垫。在瓶中制备好培养基后,将瓶子进行高压灭菌并接种真菌。然后用瓶盖密封瓶子,并用清洁空气置换瓶内空气。将提取针和气源针的表面用乙醇消毒,通过两个硅橡胶隔垫插入瓶中。将一个充满纯空气的气体采样袋连接到气源针上,在气体采样过程中,作为吹扫气向瓶中持续供应清洁空气。作为提取针,使用了一种双层吸附剂,即Carbopack-X和碳分子筛。在所研究的46种木霉菌物种中,41种检测到了3-甲基丁醇和2-甲基丁醇,2种检测到了2-戊基呋喃和6-戊基-2-吡喃。在一种植物内生真菌物种中检测到了单萜和倍半萜。在所提出的方法中,标准3-甲基丁醇和2-甲基丁醇的检测限为0.5 ng/mL。将所提出方法的性能与商业MonoTrap方法的性能进行了比较。