1Key Laboratory of Glycochemistry and Biotechnology, Ministry of Education, School of Bioengineering, Jiangnan University, Wuxi 214122, Jiangsu, China;2Shandong Fufeng Fermentation Co., Ltd., Linyi 276000, Shandong, China;3Key Laboratory of Microbial Metabolism and Green Fermentation Engineering in Inner Mongolia Autonomous Region, Inner Mongolia Fufeng Biotechnology Co., Ltd., Hohhot 010000, Inner Mongolia, China;4State Key Laboratory of Non-Grain Biomass Energy Technology, Guangxi Nongken Mingyang Biochemical Co., Ltd., Nanning 530000, Guangxi, China
This work was supported by the Construction Project of Major Scientific and Technological Innovation Base in Guangxi Zhuang Autonomous Region (2202-36-Z06-03), the Scientific Research Program of Inner Mongolia Autonomous Region (2023YFHH0088), and the Special Fund for Innovation-Driven Development of Guangxi Zhuang Autonomous Region (GuikeAA241201-1).
Replacing grain-derived carbon sources with non-grain biomass carbon sources for fermentation is a core research direction in the field of biomanufacturing. However, inhibitory byproducts present in the enzymatic hydrolysate of non-grain biomass severely restrict its practical application. We aim to reduce the dependence of xanthan gum fermentation on grain-based carbon sources, clarify the impacts of typical inhibitors from non-grain biomass enzymatic hydrolysate on xanthan gum synthesis, break through the existing application bottlenecks, and develop a green, low-loss and high-efficiency detoxification technology to overcome the inherent defects of traditional detoxification processes. In this study, we used sugarcane bagasse enzymatic hydrolysate as the fermentation carbon source, and the xanthan gum-producing strain Xanthomonas campestris 1.178 as the research object. We investigated the effects of furfural (FFR) and 5-hydroxymethylfurfural (HMF) on xanthan gum biosynthesis. To address the defects of high sugar loss and massive byproduct generation in the conventional CaO-H3PO4 detoxification process, we developed an innovative CaO-CO2 combined detoxification process, and comparatively analyzed the physicochemical properties of xanthan gum produced via the two detoxification processes. We identified that acetic acid and isovaleric acid are the key inhibitory factors in sugarcane bagasse enzymatic hydrolysate that limit xanthan gum synthesis. After CaO-CO2 treatment, we achieved retention rates of 98.23% for total sugar, 95.63% for reducing sugar, and 95.08% for glucose in the hydrolysate. We obtained a xanthan gum yield as high as 19.76 g/L, which was 19.75% higher than the yield from the CaO-H3PO4 treatment. The xanthan gum prepared in this study shared consistent infrared spectrum characteristics with commercially available xanthan gum, and we confirmed its excellent tolerance under low temperature, alkaline and high-salt conditions. The CaO-CO2 detoxification process developed in this study realizes efficient conversion of sugarcane bagasse enzymatic hydrolysate to xanthan gum, and provides a brand-new green solution for the high-value utilization of non-grain biomass.
万泽程,张云凯,王青艳,梁晓娟,赵春晓,伏广好,詹晓北,张洪涛.

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