Analysis of Microbial Diversity Dominating Nitrite Enzymatic Degradation and Acidic Degradation in the Fermentation Broth of Northeast Sauerkraut.

IF 5.1 2区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Foods Pub Date : 2024-12-23 DOI:10.3390/foods13244168
Xiangru Xu, Meng Zhang, Yuefei Tao, Wei Wei
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Abstract

Nitrite hazard is an important food safety issue in the production process of Chinese Northeastern sauerkraut, but this nitrite can be eliminated through microbial enzymatic degradation and acidic degradation as fermentation progresses. Therefore, analyzing the microbial diversity that dominates nitrite degradation in Chinese Northeastern sauerkraut can provide a reference for its safe production. In this study, based on the dynamic monitoring of nitrite concentration, pH, and the abundance of nitrite reductase genes (nirK and nirS) and the application of high-throughput sequencing technology and various statistical analysis methods, the microbial groups associated with nitrite enzymatic degradation and acidic degradation in Northeast sauerkraut fermentation broth were analyzed. During the nitrite peak period of Northeast sauerkraut fermentation broth, the nitrite concentration reached 32.15 mg/kg, the pH was 4.7, and the abundances of the nitrite reductase genes nirK and nirS were 3.0 × 104 and 4.9 × 104 copies/μL, respectively. At this stage, nitrite degradation was likely dominated by enzymatic activities. Microbial phyla such as Bacteroidetes (38.8%), Proteobacteria (19.2%), and the archaeal phylum Euryarchaeota (1.1%) showed strong correlations with nitrite. Among the genera within these three phyla, Chryseobacterium, Elizabethkingia, and Aeromonas exhibited significant differences in abundance compared to the late fermentation stage and were identified as the primary microbial groups likely driving the enzymatic degradation. During the nitrite degradation period, the nitrite concentration decreased to 0.04 mg/kg, the pH dropped to 3.6, and the abundances of nirK and nirS genes were reduced to 1.0 × 103 copies/μL. At this stage, the nitrite degradation was primarily driven by acid activity. The bacterial phylum Firmicutes (99%) exhibited a strong correlation with pH. Within this phylum, the genus Lactobacillus, which showed significant differences in abundance compared to the early fermentation stage, was identified as the primary microbial group indirectly contributing to acidic degradation. This study provides guidance for the isolation of food-grade prokaryotic microbial strains capable of nitrite degradation. Additionally, the findings offer a methodological reference for conducting future research on nitrite-degrading microorganisms in fermented vegetable broths.

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东北酸菜发酵液中主导亚硝酸盐酶解和酸解的微生物多样性分析
亚硝酸盐危害是东北酸菜生产过程中一个重要的食品安全问题,但随着发酵的进行,亚硝酸盐可以通过微生物酶降解和酸性降解来消除。因此,分析东北酸菜中主导亚硝酸盐降解的微生物多样性,可以为东北酸菜的安全生产提供参考。本研究在动态监测亚硝酸盐浓度、pH、亚硝酸盐还原酶基因(nirK和nirS)丰度的基础上,应用高通量测序技术和各种统计分析方法,对东北酸菜发酵液中亚硝酸盐酶解和酸性降解相关的微生物群进行了分析。在东北酸菜发酵液亚硝酸盐浓度达到32.15 mg/kg, pH为4.7,亚硝酸盐还原酶基因nirK和nirS丰度分别为3.0 × 104拷贝/μL和4.9 × 104拷贝/μL。在这个阶段,亚硝酸盐的降解很可能是由酶活性主导的。拟杆菌门(38.8%)、变形菌门(19.2%)和古细菌门Euryarchaeota(1.1%)与亚硝酸盐有很强的相关性。在这三个门的属中,与发酵后期相比,Chryseobacterium, Elizabethkingia和Aeromonas的丰度存在显著差异,并被确定为可能驱动酶降解的主要微生物群。亚硝酸盐降解期间,亚硝酸盐浓度降至0.04 mg/kg, pH降至3.6,nirK和nirS基因丰度降至1.0 × 103拷贝/μL。在这个阶段,亚硝酸盐的降解主要是由酸活性驱动的。细菌门厚壁菌门(99%)与ph值有很强的相关性。在该门中,乳酸菌属(Lactobacillus)的丰度与发酵早期相比有显著差异,被认为是间接促进酸性降解的主要微生物群。本研究为分离具有亚硝酸盐降解能力的食品级原核微生物菌株提供了指导。此外,该研究结果为进一步开展蔬菜发酵肉汤中亚硝酸盐降解微生物的研究提供了方法参考。
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来源期刊
Foods
Foods Immunology and Microbiology-Microbiology
CiteScore
7.40
自引率
15.40%
发文量
3516
审稿时长
15.83 days
期刊介绍: Foods (ISSN 2304-8158) is an international, peer-reviewed scientific open access journal which provides an advanced forum for studies related to all aspects of food research. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists, researchers, and other food professionals to publish their experimental and theoretical results in as much detail as possible or share their knowledge with as much readers unlimitedly as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, unique features of this journal: Ÿ manuscripts regarding research proposals and research ideas will be particularly welcomed Ÿ electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material Ÿ we also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds
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