分析物
偏最小二乘回归
校准
拉曼光谱
化学
可转让性
发酵
过程(计算)
化学计量学
过程分析技术
生物量(生态学)
生物系统
分析化学(期刊)
色谱法
计算机科学
机器学习
数学
在制品
统计
食品科学
工程类
操作系统
罗伊特
地质学
物理
光学
海洋学
生物
运营管理
作者
Maarten Klaverdijk,Marcel Ottens,Marieke E. Klijn
标识
DOI:10.1007/s00216-025-05768-5
摘要
Raman spectroscopy is a valuable analytical tool for real-time analyte quantification in fermentation processes. Quantification is performed with chemometric models that translate Raman spectra into concentration values, which are typically calibrated with process data from multiple comparable fermentations. However, process-specific models underperform for minor process variation(s) or different operation modes due to the integration of cross-correlations, resulting in low target analyte specificity. Thus, model transferability is poor and labor-intensive (re-)calibration of models is required for related processes. In this work, partial least-squares models for glucose, ethanol, and biomass were calibrated with Saccharomyces cerevisiae batch fermentation data and subsequently transferred to a fed-batch operation. To enhance model transferability without additional process runs, single compound data supplementation was performed. The supplemented models increased overall target analyte specificity and demonstrated sufficient prediction accuracy for the fed-batch process (root-mean-square errors of prediction (RMSEP) of 3.06 mM, 8.65 mM, and 0.99 g/L for glucose, ethanol, and biomass), while maintaining high prediction accuracy for the batch process (RMSEP of 1.71 mM, 4.20 mM, and 0.17 g/L for glucose, ethanol, and biomass). This work showcases that process data in combination with single compound spectra is a fast and efficient strategy to apply Raman spectroscopy for real-time process monitoring across related processes.
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