ORIGINAL RESEARCH article
Front. Microbiol.
Sec. Food Microbiology
This article is part of the Research TopicAdvances in Microbial-Based Solutions: Food Coloring, Flavoring and FragranceView all 11 articles
A new strain, Polymorphospora lycopeni A560, capable of fermentation to produce lycopene and its optimal fermentation and extraction conditions of lycopene
Provisionally accepted- Hebei University, Baoding, China
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Background: Lycopene, a vital antioxidant, can reduce oxidative damage to cells caused by reactive oxygen, prevent cancer, lower blood cholesterol levels, and mitigate cardiovascular diseases. We screened a lycopene-producing strain of genus Polymorphospora, designated A560, and discovered that its metabolic pathway lacks the lycopene β-cyclase gene crtY, which is responsible for converting lycopene into β-carotene. The absence of crtY alleviates the challenges associated with the addition of a cyclooxygenase inhibitor, which previously hindered the large-scale accumulation of lycopene in Blakeslea trispora. Method: This study was conducted to enhance lycopene production in strain A560 through a multi-stage optimization strategy, focusing on improving extraction efficiency and optimizing culture medium components. The extraction conditions were optimized by testing different solvent systems (acetone/n-hexane/ethanol), extraction temperatures, and durations. Subsequently, a uniform design (UD) was applied to systematically optimize the composition of the culture medium to maximize lycopene yield. Results: The extraction conditions were systematically optimized. A crushing duration of 4 min was identified as optimal for complete cell disruption. The most efficient solvent system was determined to be n-hexane/ethanol (2:1, v/v) at 60 °C, which yielded 62.05±4.68 mg/L of lycopene — a 37.13% increase over extraction with acetone at room temperature (45.25±0.98 mg/L). Subsequent medium optimization via uniform design revealed that soluble starch and glycerol were critical components. Cultivation in the theoretically optimized medium predicted by the model resulted in a lycopene yield of 142.54±8.58 mg/L. Finally, regulating the oxygen supply by adjusting the flask's volume of air to medium volume (Va/Vm) ratio proved crucial. The highest lycopene production of 201.44±6.23 mg/L was achieved at a Va/Vm ratio of 1.5, which marks a 224.64% improvement over the yield obtained after the initial extraction optimization (62.05±4.68 mg/L). Conclusions: The extraction and fermentation processes for lycopene production in Polymorphospora sp. A560 were successfully optimized, resulting in significantly enhanced yields. These findings highlight the potential of strain A560 as a promising microbial resource for the fermentative production of lycopene.
Keywords: Extracting conditions, LYCOPENE, Optimization of culture medium, Polymorphospora lycopeni A560, Va/Vm ratios
Received: 13 Oct 2025; Accepted: 09 Dec 2025.
Copyright: © 2025 Duan, Li, Li, Yang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Xiumin Zhang
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