“…Hence, the perceptions that: (i) BETs/BMTs occur purely through protein–protein affinity interactions & (ii) redox enzyme mediated moiety—transfers occurred purely via a Michaelis–Menten type enzyme‐substrate complex formation at a unique active site—have been superseded by the larger purview of murburn concept (Gideon et al, 2020, 2021; Manoj, 2018b; Manoj et al, 2016b; Manoj, 2020a, 2020b). Murburn models of reaction chemistry have been proposed for liver microsomal drug metabolism (Manoj et al, 2016c; Parashar & Manoj, 2021; Venkatachalam et al, 2016), aerobic respiration or mitochondrial oxidative phosphorylation (mOxPhos) (Manoj et al, 2019a, 2019b; Manoj et al, 2020a; Manoj & Bazhin, 2021), oxygenic photosynthesis or photophosphorylation (Manoj et al, 2020b; Gideon et al, 2020; Manoj & Manekkathodi, 2021; Manoj et al, 2021a‐c), hormetic/idiosyncratic dose responses (Parashar et al, 2018), photoreception (Manoj & Jacob, 2020), thermogenesis (Manoj et al, 2018), redox/ionic homeostasis and trans‐membrane potential dynamics (Manoj & Bazhin, 2021; Manoj & Tamagawa, 2021; Manoj et al, 2021; Tamagawa et al, 2021). The thermodynamically, kinetically, mechanistically and probabilistically viable physico‐chemical logic of murburn concept overwhelms the “aesthetics” stigma that “ DROS are agents of chaos ” (Jacob & Manoj, 2019).…”