Styrene measurements were performed by HS-SPME coupled to GC–MS. The chromatographic separation was carried out using an
Agilent 7890A gas chromatograph (Agilent, USA) with a
Zebron™ ZB-5MS column (30 m, 0.23 mm ID, 0.23 μm film; Phenomenex, USA). Helium gas was used as carrier gas at a 1.2 mL min
−1 flow rate. The samples were injected in split mode (100:1) and the injector temperature was held at 240 ºC. The column temperature program started at 40 ºC for 2 min and then ramped up to 240 ºC at 10 ºC per min and held there for 2 min. A mass spectrometer detector was used (model
Quattro micro GC; Waters, USA) with an electron impact ionization source of 70 eV. The temperatures of the MS source and MS transfer line were set at 240 ºC.
SPME fiber assembly Divinylbenzene/Carboxen/Polydimethylsiloxane (DVB/CAR/PDMS, 50/30 μm, 23 ga) was used for the HS-SPME procedure. The pre-incubation time was 3 min. The incubation was carried out at 40ºC and 500 rpm for 15 min. The desorption temperature was 240 ºC and the desorption time was 2 min.
Styrene and other biotransformation products present in the samples were unequivocally identified by matching the corresponding mass spectra with a standard NIST17 spectral database.
García-Franco A., Godoy P., Duque E, & Ramos J.L. (2024). Engineering styrene biosynthesis: designing a functional trans-cinnamic acid decarboxylase in Pseudomonas. Microbial Cell Factories, 23, 69.