Kornmann Henri, Rhiel Martin, Cannizzaro Christopher, Marison Ian, von Stockar Urs
Laboratory of Chemical and Biological Engineering, Swiss Federal Institute of Technology (EPFL), CH-1015 Lausanne, Switzerland.
Biotechnol Bioeng. 2003 Jun 20;82(6):702-9. doi: 10.1002/bit.10618.
An in-situ, mid-infrared sensor was used to monitor the major analyte concentrations involved in the cultivation of Gluconacetobacter xylinus and the production of gluconacetan, a food-grade exopolysaccharide. To predict the analyte concentrations, three different sets of standard spectra were used to develop calibration models, applying partial least-squares regression. It was possible to build a valid calibration model to predict the 700 spectra collected during the complete time course of the cultivation, using only 12 spectra collected every 10 h as standards. This model was used to reprocess the concentration profiles from 0 to 15 g/L of nine different analytes with a mean standard error of validation of 0.23 g/L. However, this calibration model was not suitable for real-time monitoring as it was probably based on non-specific spectral features, which were correlated only with the measured analyte concentrations. Valid calibration models capable of real-time monitoring could be established by supplementing the set of 12 fermentation spectra with 42 standards of measured analytes. A pulse of 5 g/L ethanol showed the robustness of the model to sudden disturbances. The prediction of the models drifted, however, toward the end of the fermentation. The most robust calibration model was finally obtained by the addition of 34 standard spectra of non-measured analytes. Although the spectra did not contain analyte-specific information, it was believed that this addition would increase the variability space of the calibration model. Therefore, an expanded calibration model containing 88 spectra was used to monitor, in real time, the concentration profiles of fructose, acetic acid, ethanol and gluconacetan and allowed standard errors of prediction of 1.11, 0.37, 0.22, and 0.79 g/L, respectively.
采用原位中红外传感器监测木醋杆菌培养过程中涉及的主要分析物浓度以及食品级胞外多糖葡糖醛酸聚糖的生产。为了预测分析物浓度,使用三组不同的标准光谱,通过偏最小二乘回归建立校准模型。仅使用每10小时收集的12个光谱作为标准,就有可能建立一个有效的校准模型来预测培养全过程中收集的700个光谱。该模型用于重新处理9种不同分析物从0到15 g/L的浓度曲线,平均验证标准误差为0.23 g/L。然而,该校准模型不适用于实时监测,因为它可能基于仅与测量的分析物浓度相关的非特异性光谱特征。通过用42种测量分析物标准补充12个发酵光谱集,可以建立能够实时监测的有效校准模型。5 g/L乙醇脉冲显示了模型对突然干扰的稳健性。然而,模型的预测在发酵结束时出现漂移。最终通过添加34个未测量分析物的标准光谱获得了最稳健的校准模型。尽管这些光谱不包含分析物特异性信息,但据信这种添加会增加校准模型的变异性空间。因此,使用包含88个光谱的扩展校准模型实时监测果糖、乙酸、乙醇和葡糖醛酸聚糖的浓度曲线,预测标准误差分别为1.11、0.37、0.22和0.79 g/L。