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LDL-cholesterol concentrations were calculated using the Friedewald equation (Friedewald et al, 1972).
Absolute sample concentrations were calculated using a linear model generated from a standard curve composed of authentic linalool and geraniol standards (Sigma-Aldrich, St . Louis MO, USA).
Absolute sample concentrations were calculated using a linear model generated from a standard curve composed of authentic maltotriose, maltose, glucose, and ethanol standards (Sigma-Aldrich, St . Louis MO, USA) diluted in water over a range of 0.2 20 g/L.
Inhibitory concentrations were calculated using the probit regression method [23].
Elemental concentrations were calculated using sensitivity factors provided by the instrument manufacturer.
Aqueous phase concentrations were calculated using Henry's Law constants (Shan et al. [2010a, b]).
The product and substrate concentrations were calculated using the peak areas in calibration curves equations.
Concentrations were calculated using a standard curve generated with specific standards provided by the manufacturer.
Pchlide and photoactive Pchlide concentrations were calculated using a Cary Eclipse fluorescence spectrophotometer (Varian) or UV/VIS spectrophotometer (BioTek).
Concentrations were calculated using linear regression analysis.
Cytochrome c concentrations were calculated using the standard concentration curve.
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