In vivo extraction of volatile organic compounds (VOCs) from Micro-Tom tomato flowers with multiple solid phase microextraction (SPME) fibers

2015 ◽  
Vol 93 (2) ◽  
pp. 143-150 ◽  
Author(s):  
Luis A. Cáceres ◽  
Tim W. McDowell ◽  
Ian M. Scott ◽  
Abdelali Hannoufa ◽  
Brian D. McGarvey ◽  
...  

The in vivo headspace extraction of volatile organic compounds from Micro-Tom tomato flowers was investigated using multiple solid phase microextraction (SPME) fibers of different properties to maximize the extraction selectivity for a nontargeted analysis. The three fibers used in this work were polydimethylsiloxane (PDMS), PDMS/divinylbenzene (DVB), and carboxen (CAR)/PDMS. Two sources for tomato flowers were used: Micro-Tom wild type (WT) and transgenic Micro-Tom overexpressing the carotenoid cleavage deoxygenase 1 gene. Gas chromatography–mass spectrometry (GC–MS) results demonstrated that the largest amounts of volatile organic compounds (VOCs) were observed with the PDMS/DVB fiber for both wild type and transgenic plants, but the CAR/PDMS and PDMS fibers contributed to the detection of selective compounds. Data revealed the presence of 45 VOCs from transgenic plants and 35 from the wild type when all three fibers were used together. Of the total VOCs identified, 30 were common to both types of plants, but 15 were specific to the transgenic and 5 to the wild type plants. The compounds identified from Micro-Tom flowers were mainly monocyclic and bicyclic monoterpenes and sesquiterpenes, with one alkyl benzene compound. The bicyclic monoterpenes, (1R)-α-pinene, (1S)-α-pinene, and β-pinene, were found to be the most abundant molecules present in both wild type and transgenic plants. The overall advantage of maximizing the discovery of VOCs based on the selectivity differences with three SPME fibers was evident. Such a benefit is important in the nontargeted analysis of transgenic plants for detecting the production of unexpected compounds.

2009 ◽  
Vol 4 (12) ◽  
pp. 1934578X0900401 ◽  
Author(s):  
Marisa Piovano ◽  
Juan A. Garbarino ◽  
Elizabeth Sánchez ◽  
Manuel E. Young

The compounds responsible for the characteristic odor of eight fresh non-edible Basidiomycetes fungi were evaluated. The volatile organic compounds from the fresh samples present in the headspace of a sealed vial were determined by solid-phase microextraction gas chromatography-mass spectrometry, using a PDMS/DVB fiber. A total of twenty-eight components were identified, the most frequent being 1-octen-3-ol and 3-octanone.


Separations ◽  
2018 ◽  
Vol 5 (3) ◽  
pp. 45 ◽  
Author(s):  
Kevin Eckert ◽  
David Carter ◽  
Katelynn Perrault

Volatile organic compounds (VOCs) are monitored in numerous fields using several commercially-available sampling options. Sorbent-based sampling techniques, such as solid-phase microextraction (SPME), provide pre-concentration and focusing of VOCs prior to gas chromatography–mass spectrometry (GC–MS) analysis. This study investigated the dynamics of SPME Arrow, which exhibits an increased sorbent phase volume and improved durability compared to traditional SPME fibers. A volatile reference mixture (VRM) and saturated alkanes mix (SAM) were used to investigate optimal parameters for microbiological VOC profiling in combination with GC–MS analysis. Fiber type, extraction time, desorption time, carryover, and reproducibility were characterized, in addition to a comparison with traditional SPME fibers. The developed method was then applied to longitudinal monitoring of Bacillus subtilis cultures, which represents a ubiquitous microbe in medical, forensic, and agricultural applications. The carbon wide range/polydimethylsiloxane (CWR/PDMS) fiber was found to be optimal for the range of expected VOCs in microbiological profiling, and a statistically significant increase in the majority of VOCs monitored was observed. B. subtilis cultures released a total of 25 VOCs of interest, across three different temporal trend categories (produced, consumed, and equilibrated). This work will assist in providing foundational data for the use of SPME Arrow in future microbiological applications.


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