Scale-Up of Phytosterols Bioconversion into Androstenedione.

Sonia Martínez-Cámara, Manuel de la Torre, José-Luis Barredo, Marta Rodríguez-Sáiz

Methods in molecular biology (Clifton, N.J.) 2023

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Phytosterols, coming as a by-product of vegetable oils or wood pulp, contain the cyclopentanoperhydrophenanthrene nucleus and can be bioconverted into steroid intermediates by removing the C17 side chain. This chapter shows the scale-up, from flask to bioreactor, of phytosterols bioconversion into 4-androstene-3,17-dione (androstenedione; AD) using Mycolicibacterium neoaurum B-3805. Due to the fact that phytosterols and AD are nearly insoluble in water, two-phase systems and the use of chemically modified cyclodextrins have been described as methods to solve it. Here, we use a water-oil two-phase system that allows the bioconversion of up to 20 g/L of phytosterols into AD in 5 L and 20 L bioreactors. © 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Citation

Sonia Martínez-Cámara, Manuel de la Torre, José-Luis Barredo, Marta Rodríguez-Sáiz. Scale-Up of Phytosterols Bioconversion into Androstenedione. Methods in molecular biology (Clifton, N.J.). 2023;2704:231-243