From yeast screening for suitability as single cell protein to fed-batch cultures.

IF 2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Biotechnology Letters Pub Date : 2024-10-01 Epub Date: 2024-07-13 DOI:10.1007/s10529-024-03504-0
Alexander Anderson, Adriaan Van der Mijnsbrugge, Xavier Cameleyre, Nathalie Gorret
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引用次数: 0

Abstract

Purpose: Fed-batch cultures have rarely been used in single cell protein (SCP) research. This work evaluated multiple yeast species for suitability as SCP cultivated using glucose- and sucrose-based substrate and performed in-depth studies of fed-batch SCP cultivation kinetics for selected yeasts, including determination of specific crude nitrogen-to-protein conversion factors.

Methods: SCP was cultivated using fully synthetic media in flask batch or bioreactor fed-batch cultures. Crude nitrogen and nucleic acid content were determined using the Dumas method and fluorescence assay kits, respectively.

Results: C. utilis compared favorably to other yeasts in flask batch cultures in terms of process yield (0.52 ± 0.01 gx gs-1) and crude nitrogen content (10.0 ± 0.5 and 9.9 ± 0.5%CDW for glucose and sucrose, respectively). This is the first time biomass composition data was reported for SCP cultivated in fed-batch mode. C. utilis crude nitrogen content was consistent across the tested conditions (protein content stabilized around 50%CDW in fed-batch), while that of the benchmark yeast S. cerevisiae was higher in batch cultures and at the beginning of fed-batch relative to the end (protein content decreased over time and stabilized around 43%CDW). Total nucleic acid content of the yeasts was similar (6.8%CDW and 6.3%CDW, for C. utilis and S. cerevisiae, respectively), with crude nitrogen-to-protein conversion factors of 4.97 and 5.80.

Conclusion: This study demonstrated the suitability of C. utilis as SCP, notably the robustness of its crude nitrogen content (as an indicator of protein content) across batch and fed-batch conditions, compared to that of the benchmark yeast S. cerevisiae.

Abstract Image

从筛选适合作为单细胞蛋白质的酵母到饲料批量培养。
目的:在单细胞蛋白(SCP)研究中,很少使用间歇培养法。这项工作评估了多个酵母物种是否适合作为使用葡萄糖和蔗糖基底培养的 SCP,并对选定酵母的喂养批次 SCP 培养动力学进行了深入研究,包括确定特定的粗氮-蛋白质转换因子:方法:在烧瓶批量或生物反应器喂料批量培养中使用全合成培养基培养 SCP。分别使用杜马斯法和荧光检测试剂盒测定粗氮和核酸含量:结果:在烧瓶批量培养中,C. utilis 的加工产量(0.52 ± 0.01 gx gs-1)和粗氮含量(葡萄糖和蔗糖的粗氮含量分别为 10.0 ± 0.5 和 9.9 ± 0.5%CDW)均优于其他酵母菌。这是首次报道以饲料批量模式培养的 SCP 的生物量组成数据。C. utilis 的粗氮含量在所有测试条件下都保持一致(蛋白质含量在喂养批次中稳定在 50%CDW 左右),而基准酵母 S. cerevisiae 的粗氮含量在批次培养和喂养批次开始阶段相对于结束阶段较高(蛋白质含量随着时间的推移而降低,稳定在 43%CDW 左右)。两种酵母的总核酸含量相似(C. utilis 和 S. cerevisiae 分别为 6.8%CDW 和 6.3%CDW),粗氮-蛋白质转换系数分别为 4.97 和 5.80:本研究证明了 C. utilis 作为 SCP 的适用性,特别是与基准酵母 S. cerevisiae 相比,其粗氮含量(作为蛋白质含量的指标)在批次和喂养批次条件下的稳定性。
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来源期刊
Biotechnology Letters
Biotechnology Letters 工程技术-生物工程与应用微生物
CiteScore
5.90
自引率
3.70%
发文量
108
审稿时长
1.2 months
期刊介绍: Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them. All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included. Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields. The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories. Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.
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