Using pre-fermented sugar beet pulp as a growth medium to produce Pleurotus ostreatus mycelium for meat alternatives

IF 5 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY International journal of food microbiology Pub Date : 2024-08-15 DOI:10.1016/j.ijfoodmicro.2024.110872
Sanne Kjærulf Todorov , Frantiska Tomasikova , Mikkel Hansen , Radhakrishna Shetty , Celia L. Jansen , Charlotte Jacobsen , Timothy John Hobley , René Lametsch , Claus Heiner Bang-Berthelsen
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Abstract

This study aimed to determine the compatibility of pre-fermented sugar beet pulp to support the growth of Pleurotus ostreatus mycelium in submerged fermentation. The goal was to create a meat alternative based on mycelial-fermented pulp. It was further explored whether pre-fermentation with lactic acid bacteria (LAB) on the pulp increased meat-like properties, such as aroma, springiness, and hardness, in the final product. Three strains were selected from a high throughput screening of 105 plant-derived LAB based on their acidification and metabolite production in the pulp. Two homofermentative strains (Lactococcus lactis) and one heterofermentative strain (Levilactobacillus brevis) were selected based on their low ethanol production, high lactic acid production, and overall acidification of the pulp. Mycelium of P. ostreatus was grown in submerged fermentations on the pre-fermented pulp, and the biomass was removed by centrifugation. The fungal strain consumed all available sugars and acids and released arabinose to the media. Volatiles were detected using GC–MS, and a large increase in concentrations of hexanal, 1-octen-3-ol, and 2-octenal was measured. Concentration of 1-octen-3-ol was lower in the pre-fermented samples vs. the non-pre-fermented. LC-MS amino acid analysis showed the presence of all essential amino acids on day 0 and 7 of fermentation. The highest concentration of amino acids was for glutamic acid/glutamine and aspartic acid/asparagine. A decrease in all amino acids after 7 days of fungal fermentation was measured for all fermentations. The decrease was more significant for pre-fermented samples. This was also confirmed through a total protein determination, except for samples pre-fermented with Lactococcus lactis strain NFICC142 which increased in total protein content after fungal fermentation. The protein digestibility increased after fungal fermentation, and the highest increase was seen for non-pre-fermented samples. The springiness of the fermented product indicated similarities to meat alternatives, while the hardness was much lower than other meat alternatives. The results indicate that dried sugar beet pulp can be used for submerged cultivation of P. ostreatus, but that pre-fermentation does not improve the physical or nutritional properties of the end product significantly, except for an increased protein content for NFICC142 pre-fermented media. This is the first known attempt to use LAB and P. ostreatus in mixed fermentation to produce fungal mycelium, as well as the first attempt at using SBP in a liquid fermentation for mycelial production of P. ostreatus.

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利用预发酵甜菜浆作为生长介质,生产肉类替代品中的褶菌菌丝体
这项研究旨在确定预发酵甜菜浆在浸没式发酵中支持壳斗菌菌丝生长的兼容性。目的是在菌丝发酵纸浆的基础上创造一种肉类替代品。研究还进一步探讨了用乳酸菌(LAB)对纸浆进行预发酵是否会增加最终产品的肉类特性,如香味、弹牙和硬度。在对 105 种植物源 LAB 进行高通量筛选后,根据它们在果肉中的酸化作用和代谢物产生情况,选出了三株菌株。两株同发酵菌株(乳酸乳球菌)和一株异发酵菌株(乳酸左旋乳杆菌)是根据它们的低乙醇产量、高乳酸产量和纸浆的整体酸化效果筛选出来的。在预发酵纸浆的浸没式发酵过程中生长了奥斯特菌(P. ostreatus)菌丝,并通过离心去除生物质。真菌菌株消耗所有可用的糖和酸,并向培养基释放阿拉伯糖。使用气相色谱-质谱仪检测挥发性物质,结果发现己醛、1-辛烯-3-醇和 2-辛烯醛的浓度大幅上升。与非预发酵样品相比,预发酵样品中 1-辛烯-3-醇的浓度较低。LC-MS 氨基酸分析表明,在发酵的第 0 天和第 7 天,所有必需氨基酸都存在。氨基酸浓度最高的是谷氨酸/谷氨酰胺和天冬氨酸/天冬酰胺。真菌发酵 7 天后,所有发酵物中所有氨基酸的含量都有所下降。预发酵样品的下降幅度更大。总蛋白质的测定也证实了这一点,但用乳酸乳球菌菌株 NFICC142 预发酵的样品除外,它们的总蛋白质含量在真菌发酵后有所增加。经过真菌发酵后,蛋白质的消化率提高了,未经过预发酵的样品蛋白质消化率提高得最快。发酵产品的弹力与肉类替代品相似,而硬度则远低于其他肉类替代品。研究结果表明,干甜菜浆可用于浸没式培养奥斯特氏菌,但除了 NFICC142 预发酵培养基的蛋白质含量增加外,预发酵并不能显著改善最终产品的物理或营养特性。这是已知的首次尝试使用 LAB 和 P. ostreatus 混合发酵生产真菌菌丝,也是首次尝试在液体发酵中使用 SBP 生产 P. ostreatus 菌丝。
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来源期刊
International journal of food microbiology
International journal of food microbiology 工程技术-食品科技
CiteScore
10.40
自引率
5.60%
发文量
322
审稿时长
65 days
期刊介绍: The International Journal of Food Microbiology publishes papers dealing with all aspects of food microbiology. Articles must present information that is novel, has high impact and interest, and is of high scientific quality. They should provide scientific or technological advancement in the specific field of interest of the journal and enhance its strong international reputation. Preliminary or confirmatory results as well as contributions not strictly related to food microbiology will not be considered for publication.
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