Currently, astaxanthin demand is fulfilled by chemical synthesis using petroleum-based feedstocks. As such, alternative pathways of natural astaxanthin production attracts much research interest. This study aimed at optimising bioreactor operation parameters for astaxanthin production and evaluating strategies for its subsequent extraction. The effect of pH and agitation was evident, as a significant reduction in both biomass and astaxanthin production was observed when the culture pH was not controlled and a low agitation speed was applied. At controlled pH conditions and a high agitation speed, a significant increase in biomass (16.4 g/L) and astaxanthin production (3.6 mg/L) was obtained. Enzymatic yeast cell lysis using two commercial enzymes (Accellerase 1500 and Glucanex) was optimised using the central composite design of experiment (DoE). Accellerase 1500 led to mild cell disruption and only 9% (w/w) astaxanthin extraction. However, Glucanex treatment resulted in complete astaxanthin extractability, compared to standard extraction method (DMSO/acetone). When supercritical CO 2 was employed as an extraction solvent in Accellerase-pre-treated Xanthophyllomyces dendrorhous cells, astaxanthin extraction increased 2.5-fold. Overall, the study showed that extraction conditions can be tailored towards targeted pigments present in complex mixtures, such as in microbial cells.Microorganisms 2020, 8, 430 2 of 18 up and commercialisation of astaxanthin production [3-5], while its extraction and purification still contributes to the overall complexity and cost of the whole production process.Various cultivation modes, including batch, fed-batch, and continuous, have been investigated for carotenoid production in yeasts, either in the lab or at the pilot scale [6][7][8]. In the case of some yeast species cultivated on batch mode, high initial carbon concentrations (usually glucose) result in suppression of cell growth as well as product formation due to the Crabtree effect [9,10]. It has been demonstrated that X. dendrorhous undergoes the Crabtree effect, a phenomenon where cells metabolically switch to fermentative metabolism leading to ethanol production even under ample oxygen supply when initial glucose present is above a given threshold (strain dependent) [10,11]. Fed-batch cultivation mode is considered as an appropriate strategy to overcome such issues, as it allows the addition of one or more nutrients to the reactor during fermentation in order to maintain the concentration of the substrate below its inhibitory levels [12]. Furthermore, with regards to media optimization, low concentrations of ammonium and phosphate have been reported to be favourable towards astaxanthin production, whereas increased levels of citrate in the growth medium have been shown to stimulate astaxanthin production, as citrate can act as a carbon source towards astaxanthin biosynthesis in Phaffia rhodozyma [13]. The effect of light on astaxanthin productivity in several yeast and microalgae strains has been also extensively studied [1...
Rapeseed meal, a by-product of oil processing industry, was evaluated as a substrate for astaxanthin production by the yeast Xanthophyllomyces dendrorhous DSMZ 5626. Four commercial enzymes were tested at different concentrations (1-15 %, v/v) for their ability to break down the cellulosic and hemicellulosic compounds of rapeseed meal into fermentable sugars. Viscozyme® L and cellulase demonstrated the highest glucose recovery yields (47-52%, w/w for 15 % (v/v) of enzyme loading) with 7-11 g/l of net glucose released in the hydrolysates. Pectinase and Accellerase® hydrolysates supported the best cell growth and astaxanthin production in batch shake flask cultures, with maximum biomass of 26 g/l and 15 g/l, respectively, and astaxanthin yields (YP/X) of 258 to 332 µg per g of biomass. In batch bioreactor trials, pectinase hydrolysates resulted in high biomass (42 g/l) and astaxanthin production (11 mg/l) aided by the presence of glycerol (originating from the enzyme formulation) which served as additional energy and carbon source. Finally, simple glass beads disruption lead into satisfactory astaxanthin extraction (95 %, w/w) in acetone. The findings of this study generate knowledge towards scale-up potential of microbial astaxanthin production using rapeseed meal hydrolysate as fermentation feedstock.
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