da Costa Fonseca Ynara, Bahule Celina Eugenio, Herrera Hector, da Silva Martins Luiza Helena, Lopes Alessandra Santos, Cassoli Juliana Silva, Trindade Felipe Costa, Chagas da Costa Isa Rebecca, Henrique de Oliveira Costa Paulo, Oliveira Guilherme, Borges da Silva Valadares Rafael
Graduate Program in Agricultural Applied Biotechnology, Federal Rural University of Amazonia, President Tancredo Neves Ave, 2501, Belém, CEP 66.077-830, Brazil.
Vale Institute of Technology, Boaventura da Silva Street 955, Belém, CEP 66050-090, Brazil.
Heliyon. 2024 Nov 19;10(23):e40542. doi: 10.1016/j.heliyon.2024.e40542. eCollection 2024 Dec 15.
To gain insight into the active microbiota during spontaneous fermentation of L., this study assessed protein diversity during 120 h using a combined metabarconding and metaproteomics approach. During the first days of fermentation, most of the peptides were associated with and yeast (0-72 h). Peptides associated with bacteria became more abundant after 72 h of fermentation, coinciding with a decrease in peptides associated with cocoa (96-120 h). In addition to the known microorganisms involved in fermentation, such as , and , novel genera were also metabolically active, including , , and .. The results showed a consistency in the main genera detected by both techniques, but the identification of unexplored genera such as , , and , among others, suggests that this omics approach needs to be used together for more comprehensive results on spontaneous fermentation. In conclusion, studies combining techniques such as metabarcoding and metaproteomics should be considered in fermentation studies, as a single technique would result in omissions regarding the activity of certain microorganisms that may be important for the course of spontaneous fermentation.
为深入了解L.自发发酵过程中的活性微生物群,本研究采用元条形码和元蛋白质组学相结合的方法,评估了120小时内的蛋白质多样性。在发酵的最初几天,大多数肽与可可和酵母相关(0 - 72小时)。发酵72小时后,与细菌相关的肽变得更加丰富,同时与可可相关的肽减少(96 - 120小时)。除了参与发酵的已知微生物,如、和外,新的属也具有代谢活性,包括、、和。结果表明,两种技术检测到的主要属具有一致性,但对未探索的属如、、和等的鉴定表明,这种组学方法需要一起使用,以获得关于自发发酵更全面的结果。总之,在发酵研究中应考虑结合元条形码和元蛋白质组学等技术的研究,因为单一技术可能会遗漏某些对自发发酵过程可能很重要的微生物的活性。