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The ketone bodies produced and released by glycolytic fat cells are the ideal fuel for ATP production and they can be burned more efficiently than other mitochondrial substrates, even during hypoxia, potentially allowing the tumor grow when without adequate blood supply (279)

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However, because we thought the cause of these low glutathione yields was excess l-Ser accumulation in cells by simultaneous overexpression of l-Ser biosynthetic genes, we constructed SHM2 and/or CYS4 overexpressing strains using the GCI/ SER3 / SER33 and GCI/ SERs as the platform strains and examined glutathione production of these strains (Fig

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