BECAS
ANDRADA Lidia Estefania
congresos y reuniones científicas
Título:
ANTIOXIDANT PROFILE AND BACTERIAL COMMUNITY COMPOSITION OF CORN STOVER SILAGES INOCULATED WITH FERULIC ACID ESTERASE-PRODUCING LACTOBACILLI
Autor/es:
ANDRADA, ESTEFANÍA; MECHOUD, MÓNICA ; SUÁREZ, NADIA ELINA; ABEIJÓN MUKDSI, MARÍA CLAUDIA; MÁRQUEZ, ANTONELA; RUSSO, MATÍAS; LEBLANC, JEAN GUY; MEDINA, ROXANA BEATRIZ
Lugar:
Chapadmalal
Reunión:
Congreso; XVIII Congreso de la Sociedad Argentina de Microbiología General; 2023
Institución organizadora:
Sociedad Argentina de Microbiología General
Resumen:
Bacterial inoculants are frequently used to improve the fermentation quality of silages, but their impact on the bioactive compounds’ content is still unknown. Ferulic acid esterase-producing (FAE+) lactobacilli can potentially increase the release of ferulic acid (FA) from its esterified forms in forages. FA is a well-known antioxidant compound, and evidence suggests it can also act as a growth promoter for livestock. Metagenomic analysis applied to silages is a recent approach that allows a better understanding of the ensiling process and the efficacy of its modulation through microbial additives. In this work, we evaluated the effects of FAE+ lactobacilli on functional characteristics and the bacterial community composition of corn stover silages. Laboratory-scale silages were inoculated with FAE+ strains: Lactiplantibacillus (L.) plantarum CRL2241 (LP1), Lactiplantibacillus (L.) plantarum CRL046 (LP2), Lactobacillus johnsonii CRL2240 (LJ) or Levilactobacillus brevis CRL2239 (LB). The inoculation rate was 1×106 CFU g fresh matter-1, using bacterial cell suspensions. The control group (UN, uninoculated) was prepared using a sterile suspension buffer. At 60 days of ensiling, total phenolic content (TPC, using Folin-Ciocalteu reagent), DPPH-scavenging activity, and free FA content (using HPLC) was determined in methanolic extracts. Total DNA was extracted from ground, lyophilized samples of all groups except LP2. Amplification of the V3-V4 hypervariable region of the 16S rRNA was performed using 2x KAPA HiFi HotStart ReadyMix (Roche, USA) and standard primers (341F and 805R). Sequencing was performed in a NextSeq 550 system (Illumina, UK). TPC was reduced in LP1, LP2, and LJ silages in comparison to UN (ANOVA followed by Tukey’s test, p