“…Direct deprotonation results in the formation of an acyclic monoterpene hydrocarbon [e.g., β‐myrcene, ( Z )‐β‐ocimene or ( E )‐β‐ocimene], while water capture with subsequent deprotonation leads to the formation of acyclic alcohol [geraniol, nerol, (−)‐(3 R )‐linalool, or (+)‐(3 S )‐linalool] (Figure 3, inset 1). MTSs that produce one of these acyclic monoterpenes preferentially have been characterized across the angiosperm lineage (Abbas et al., 2019; Aharoni et al., 2004; Arimura et al., 2004, 2008; Aros et al., 2012; Ashaari et al., 2020; Bin et al., 2023; Bohlmann et al., 2000; Booth et al., 2017; Cao et al., 2014; Chen et al., 2003, 2010, 2018, 2023; Dudareva et al., 1996, 2003; Fäldt et al., 2003; Fan et al., 2023; Gao et al., 2018; Günnewich et al., 2007; Han et al., 2023; Hosoi et al., 2004; Huang et al., 2018, 2021, 2022; Ibdah et al., 2022; Iijima, Davidovich‐Rikanati, et al., 2004; Iijima, Gang, et al., 2004; Ito & Honda, 2007; Javedan Asl et al., 2015; Jia et al., 1999; Jing‐Jing et al., 2014; Magnard et al., 2018; Masumoto et al., 2010; Mei et al., 2017; Nagegowda et al., 2008; Nawade et al., 2020; Önder et al., 2021; Ruan et al., 2016; Shimada et al., 2004, 2005; Sugiura et al., 2011; van Schie et al., 2007; Wang & Ito, 2014; Yahyaa et al., 2015; Yang et al., 2005, 2013; Yuan et al., 2008; Yue et al., 2014; Zager et al., 2019; Zeng et al., 2016; Zhang et al., …”