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Figure 1: Phosphoethanolamine Transfer Reaction Catalysed by MCR-1.
Charge transfer reaction 1 was found to dominate the overall charge transfer reaction under cathodic polarization.
Thus, a direct polarization transfer reaction from 1H to 19F might become possible (see Fig. 6b).
One structure captures a phosphorylated form representing the first intermediate in the transfer reaction.
Taken together, these data make uncertain the role of this metal ion in the PTE transfer reaction.
Under anodic polarization, a change in the dominating charge transfer reaction from charge transfer reaction 1 to charge transfer reaction 2 was found when increasing the H2O partial pressure.
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Proton transfer reaction-mass spectrometry (PTR-MS) was used to identify and quantify major VOCs.
Volatile compounds were measured in real time using a proton transfer reaction-mass spectrometer.
Proton Transfer Reaction-Mass Spectrometry (PTR-MS) analyses revealed that damaged Brassica roots emit sulfur-containing volatiles.
This represents a proton-transfer reaction from A1 to B2, producing B1 and A2.
Further fluctuations in protein structure around the neutral cis chromophore are required to form a new intermediate, which promotes the final proton-transfer reaction.
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