4.7 Article

A real-time monitoring system for automatic morphology analysis of yeast cultivation in a jar fermenter

期刊

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
卷 106, 期 12, 页码 4683-4693

出版社

SPRINGER
DOI: 10.1007/s00253-022-12002-0

关键词

High-speed camera; Real-time monitoring; Microfluidic device; Morphology; Jar fermenter; Microscopy

资金

  1. New Energy and Industrial Technology Development Organization (NEDO, Kanagawa prefecture, Japan) [JPNP19001]

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By developing a system with a microfluidic device and a high-speed camera, we were able to acquire real-time high-definition morphological information of yeast cells and monitor the cultivation process. The system successfully captured the morphological changes of yeast cells during ethanol fermentation, suggesting new possibilities for controlling microbial fermentation using morphological information.
The monitoring of microbial cultivation in real time and controlling their cultivation aid in increasing the production yield of useful material in a jar fermenter. Common sensors such as dissolved oxygen (DO) and pH can easily provide general-purpose indexes but do not reveal the physiological states of microbes because of the complexity of measuring them in culture conditions. It is well known from microscopic observations that the microbial morphology changes in response to the intracellular state or extracellular environment. Recently, studies have focused on rapid and quantitative image analysis techniques using machine learning or deep learning for gleaning insights into the morphological, physiological or gene expression information in microbes. During image analysis, it is necessary to retrieve high-definition images to analyze the microbial morphology in detail. In this study, we have developed a microfluidic device with a high-speed camera for the microscopic observation of yeast, and have constructed a system capable of generating their morphological information in real-time and at high definition. This system was connected to a jar fermenter, which enabled the automatic sampling for monitoring the cultivation. We successfully acquired high-definition images of over 10,000 yeast cells in about 2.2 s during ethanol fermentation automatically for over 168 h. We recorded 33,600 captures containing over 1,680,000 cell images. By analyzing these images, the morphological changes of yeast cells through ethanol fermentation could be captured, suggesting the expansion of the application of this system in controlling microbial fermentation using the morphological information generated.

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