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利用筛选、统计评估和验证优化小球藻 HS2 的异养培养。

Optimization of heterotrophic cultivation of Chlorella sp. HS2 using screening, statistical assessment, and validation.

机构信息

Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science & Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.

Department of Chemistry and Energy Engineering, Sangmyung University, 20 Hongimun 2-gil, Jongno-gu, Seoul, 03016, Republic of Korea.

出版信息

Sci Rep. 2019 Dec 18;9(1):19383. doi: 10.1038/s41598-019-55854-9.

Abstract

The heterotrophic cultivation of microalgae has a number of notable advantages, which include allowing high culture density levels as well as enabling the production of biomass in consistent and predictable quantities. In this study, the full potential of Chlorella sp. HS2 is explored through optimization of the parameters for its heterotrophic cultivation. First, carbon and nitrogen sources were screened in PhotobioBox. Initial screening using the Plackett-Burman design (PBD) was then adopted and the concentrations of the major nutrients (glucose, sodium nitrate, and dipotassium phosphate) were optimized via response surface methodology (RSM) with a central composite design (CCD). Upon validation of the model via flask-scale cultivation, the optimized BG11 medium was found to result in a three-fold improvement in biomass amounts, from 5.85 to 18.13 g/L, in comparison to a non-optimized BG11 medium containing 72 g/L glucose. Scaling up the cultivation to a 5-L fermenter resulted in a greatly improved biomass concentration of 35.3 g/L owing to more efficient oxygenation of the culture. In addition, phosphorus feeding fermentation was employed in an effort to address early depletion of phosphate, and a maximum biomass concentration of 42.95 g/L was achieved, with biomass productivity of 5.37 g/L/D.

摘要

异养培养微藻具有许多显著的优点,包括能够实现高培养密度以及稳定且可预测地生产生物质。在本研究中,通过优化其异养培养的参数来探索 HS2 小球藻的全部潜力。首先,在 PhotobioBox 中筛选了碳源和氮源。然后采用 Plackett-Burman 设计(PBD)进行初步筛选,并通过中心复合设计(CCD)的响应面法(RSM)优化了主要营养物(葡萄糖、硝酸钠和磷酸二氢钾)的浓度。通过摇瓶培养验证模型后,发现与含有 72 g/L 葡萄糖的未优化 BG11 培养基相比,优化后的 BG11 培养基可使生物质量增加三倍,从 5.85 增至 18.13 g/L。将培养扩大到 5 L 发酵罐中,由于培养物的氧气供应更加高效,从而使生物质浓度大大提高,达到 35.3 g/L。此外,还采用磷补料发酵来解决磷酸盐早期耗尽的问题,实现了 42.95 g/L 的最大生物质浓度,生物质生产率为 5.37 g/L/D。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0e8/6920485/9d4f028c52e4/41598_2019_55854_Fig1_HTML.jpg

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