Near real-time quantification of microbial volatile organic compounds from mycoparasitic fungi: Potential for advanced monitoring and pest control

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-07-10 DOI:10.1016/j.jchromb.2024.124237
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Abstract

Microbial volatile organic compounds (MVOCs) are thought to play a key role in the interactions between mycoparasitic fungi, such as the biocontrol agent Trichoderma atroviride (T. atroviride), and their environment. However, the analysis of MVOC emissions from fungal samples is challenging because of low analyte concentrations, typically in the ppbV-range, and the complex chemical nature of biological samples. In a recent study using proton transfer reaction-time of flight-mass spectrometry (PTR-ToF-MS) to determine MVOC emissions from T. atroviride, many product ions were unspecific, as they could arise from a large number of possible analytes. The aim of the present study was to determine whether fast gas chromatography (fast-GC) coupled to PTR-ToF-MS could be used to overcome this issue and constitute a suitable on-line, near real-time method to identify and quantify fungal MVOC emissions in the ppbV-to-ppmV regime. Using gas standards of eleven MVOCs known to be emitted by T. atroviride such as 6-amyl-α-pyrone (6-PP), 2-pentylfuran, 1-octen-3-ol, 2-heptanone, 3-octanone, 2-methyl-1-propanol, 2-pentanone, 3-methyl-1-butanol, 3-methylbutanal, acetone and ethanol, we developed a fast-GC method with a total runtime of 180 s which significantly enhances the analytical specificity of PTR-ToF-MS compared to conventional PTR-ToF-MS without fast-GC separation. Limits of detection were on the order of 0.1–4 ppbV. The increased analytical specificity demonstrated notable benefits, especially for MVOCs having partially overlapping distributions of product ions when analyzed directly using PTR-ToF-MS.

In order to demonstrate the applicability of the analytical method, we analysed T. atroviride samples in four biological replicates twice daily over a duration of five days. Using the fast-GC method, nine out of the eleven MVOC species considered in this study in the headspace of T. atroviride could be identified and quantified and their time evolution over the five-day incubation period determined. The measured volume mixing ratios (VMRs) ranged from single-digit ppbV (2-pentylfuran) up to few ppmV (6-PP and ethanol), with the other compounds in the 10-to-100-ppbV range (1-octen-3-ol, 2-heptanone, 2-methyl-1-propanol, 3-methyl-1-butanol, 3-methylbutanal and acetone).

Our results suggest that fast-GC-PTR-ToF-MS is a method well-suited for the analysis of gas-phase samples of biological origin, including but not limited to (mycoparasitic) fungi, in a wide range of VMRs from sub-ppbV to few-ppmV.

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近实时定量分析寄生真菌的微生物挥发性有机化合物:先进监测和害虫控制的潜力
微生物挥发性有机化合物(MVOCs)被认为在寄生真菌(如生物防治剂阿特罗维里德毛霉(T. atroviride))与其环境的相互作用中起着关键作用。然而,由于分析物浓度较低,通常在 ppbV 范围内,而且生物样本的化学性质复杂,因此分析真菌样本中的 MVOC 排放物具有挑战性。最近的一项研究使用质子转移反应飞行时间质谱法(PTR-ToF-MS)来测定 T. atroviride 真菌的 MVOC 排放,结果发现许多产物离子并不特异,因为它们可能来自大量可能的分析物。本研究的目的是确定快速气相色谱法(fast-GC)与 PTR-ToF-MS 联用是否能克服这一问题,并成为一种合适的在线近实时方法,用于鉴定和量化 ppbV 至ppmV 范围内的真菌 MVOC 排放。使用已知由 T. atroviride 真菌排放的 11 种 MVOC 气体标准物质,如 6-(2)-(3)-(4)atroviride)排放的 11 种 MVOC 气体标准,如 6-amyl-α-pyrone(6-PP)、2-戊基呋喃、1-辛烯-3-醇、2-庚酮、3-辛酮、2-甲基-1-丙醇、2-戊酮、3-甲基-1-丁醇、3-甲基丁醛、丙酮和乙醇、我们开发了一种总运行时间为 180 秒的快速-气相色谱方法,与没有快速-气相色谱分离的传统 PTR-ToF-MS 相比,该方法显著提高了 PTR-ToF-MS 的分析特异性。检测限约为 0.1-4 ppbV。为了证明该分析方法的适用性,我们在五天的时间里每天两次对四个生物重复样本中的 T. atroviride 进行了分析。使用快速 GC 方法,本研究中考虑的 11 种 MVOC 物种中,有 9 种可以在阿特罗维里德顶空进行鉴定和定量,并确定了它们在五天培养期内的时间变化情况。测得的体积混合比(VMRs)从个位数 ppbV(2-戊基呋喃)到几个 ppmV(6-PP 和乙醇)不等,其他化合物在 10 到 100 ppbV 之间(1-辛烯-3-醇、2-庚酮、2-甲基-1-丙醇、3-甲基-1-丁醇、3-甲基丁醛和丙酮)。我们的研究结果表明,快速-GC-PTR-ToF-MS 是一种非常适合分析生物源气相样品的方法,包括但不限于(寄生真菌),其 VMR 范围很广,从亚ppbV 到几ppmV 不等。
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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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