Crown ether dopant to reduce ion suppression and improve detection in the liquid microjunction surface sampling probe

Abstract

RationaleSodium and potassium are required in agar media for the growth of some microorganisms (e.g., marine bacteria). However, alkali cations are a significant source of contamination for mass spectrometry causing ion suppression and adduct formation. Conventionally, salts can be removed before mass spectrometric analysis with appropriate and often lengthy sample preparation. The direct mass spectrometric sampling of bacterial colonies grown on agar media seeks to minimize or eliminate sample preparation to improve workflow. However, this may exacerbate ion suppression and contamination since these metal cations will degrade spectral quality and limit the rapid profiling of microbial metabolites. Different approaches are needed to sequester sodium and potassium ions to minimize unwanted background interferences. Herein, we use crown ethers (CEs) in combination with a liquid microjunction surface sampling probe (LMJ‐SSP) to directly sample the surface of the bacterial colonies from two marine bacteria species (Pseudoalteromonas rubra DSM6842 and Pseudoalteromonas tunicata DSM 14096). CEs (e.g., 18‐crown‐6 or 15‐crown‐5) are added to the carrier solvent of the LMJ‐SSP, the chemical noise is reduced, and spectra are easier to interpret.MethodsThe liquid microjunction formed at the tip of LMJ‐SSP was used to directly touch bacterial colonies on agar. The carrier solvent was either methanol (100%) or methanol: H2O (50:49.9%) with or without 0.01% CEs. Information‐theoretic measures are employed to investigate qualitative changes between spectra before and after adding CEs.ResultsOur work demonstrates the capability of CEs to reduce background interferences within the direct profiling of bacterial colonies from agar plates. The data obtained from both P. rubra DSM6842 and P. tunicata DSM 14096 show that CEs can be used to mitigate the salty background and improve compound detection.ConclusionOur approach can be implemented in natural product discovery using LMJ‐SSP to allow fast and accurate detection of interesting/novel compounds.