植物性肉类替代品在冷藏过程中的腐败微生物群落特征。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Mehmet Dogan, David A Mann, Xiangyu Deng
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引用次数: 0

摘要

植物性肉类替代品(pbma),主要来源于豌豆或大豆蛋白,越来越受欢迎和市场份额,但其腐败生态学仍未得到充分研究。为了解决这一知识差距,我们分析了在美国销售的12种冷藏pbma(6种豌豆基肉类[PBMs]和6种大豆基肉类[SBMs],每一种都是碎肉和汉堡形式)在冷藏货架展示和延长储存期间的细菌和真菌群落。在店内解冻和过了保质期后,产品的微生物负荷迅速上升,而且各不相同,这强调了在商店和家中处理pbma的必要性,就像处理任何其他高度易腐的食品一样。大豆和豌豆基质显示出不同的腐败菌群组合和演替模式,表明蛋白质来源决定了腐败轨迹。我们的研究结果强调了植物性肉类替代品(pbma)的腐败是由蛋白质来源决定的,大豆和豌豆产品在成分组成和腐败微生物群的驱动下表现出不同的微生物轨迹和酸度特征。这些与成分相关的腐败模式的识别为pbma的定制和精确的腐败管理奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of the spoilage microbial communities in plant-based meat alternatives during refrigerated storage.

Plant-based meat alternatives (PBMAs), primarily derived from pea or soy proteins, are gaining popularity and market share, yet their spoilage ecology remains understudied. To address this knowledge gap, we profiled the bacterial and fungal communities of 12 refrigerated PBMAs commonly sold in the United States (six pea-based meats [PBMs] and six soy-based meats [SBMs], each in ground and burger forms) during refrigerated shelf display and extended storage. Microbial loads rose rapidly and heterogeneously across products after in-store thawing and past sell-by dates, underscoring the need to handle PBMAs like any other highly perishable food, both in stores and at home. Soy and pea-based matrices exhibited distinct patterns of spoilage microbiota assemblage and succession, suggesting that the protein source shapes spoilage trajectories.IMPORTANCEOur findings highlight that spoilage of plant-based meat alternatives (PBMAs) is shaped by the protein source, with soy- and pea-based products exhibiting distinct microbial trajectories and acidity profiles driven by both ingredient composition and spoilage microbiota. Identification of these ingredient-associated spoilage patterns lays the foundation for tailored and precision spoilage management for PBMAs.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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