The flavor variation among different tea plant cultivars significantly influences their economic value. ‘Huangjinya’ (HJY), a typical light-sensitive etiolated tea cultivar, is prized for its fresh and mellow taste with low bitterness and astringency, and commands a high market value, serving as excellent germplasm for breeding superior-flavor tea varieties. Previous studies have largely focused on the mechanisms underlying fresh and umami tastes, whereas the regulatory mechanisms underlying bitterness and astringency remain poorly understood. In this study, two tea plant (Camellia sinensis (L.) O. Kuntze) cultivars with distinct bitterness and astringency phenotypes, namely ‘Fuxuan 9’ (FX) and HJY, were used to investigate the formation mechanism of reduced bitterness and astringency through integrated metabolomic and transcriptomic analyses. Metabolomic profiling identified 601 differentially accumulated metabolites between the two cultivars, which were significantly enriched in the flavonoid biosynthesis pathway. Notably, although the total flavonoid content was higher in HJY, the accumulation of non-esterified catechins (C, EC, EGC), which are key contributors to bitterness, was significantly lower than in FX. By contrast, the levels of esterified catechins (EGCG, GCG) showed no marked differences between cultivars. This distinct accumulation pattern provides a metabolic basis potentially associated with the reduced bitterness and astringency in HJY. Transcriptomic analysis revealed that the catechin biosynthetic gene CsLAR was significantly down-regulated in HJY, consistent with the reduced accumulation of non-esterified catechins. Promoter cloning and functional validation confirmed that the CsLAR promoters in both cultivars were active, which differed by only one regulatory element. Under shading treatment, CsLAR expression in HJY was more sensitive to light and decreased more markedly, suggesting that the expression of CsLAR may be regulated by transcription factors. Furthermore, 385 differentially expressed transcription factors were identified, with predicted binding sites in the CsLAR promoter region, implying their potential involvement in modulating catechin accumulation through modulation of CsLAR expression. Together, these multi-omics findings reveal molecular features potentially contributing to the low bitterness and astringency of HJY, providing a theoretical basis and candidate regulators for breeding tea cultivars with improved flavor profiles.
Ling-Hui Wang, Quan Xu, Miao Xu et al.· Plants· 0 citations
ABSTRACT Effective probiotic therapy for colitis is hindered by the harsh gastrointestinal (GI) physiologic and pathologic environment, including acidic pH, bile salts, elevated reactive oxygen species (ROS), mucus depletion, and dysbiosis. To address these challenges, we developed a novel “drug carrier‐integrated” oral probiotic delivery system—L. reuteri@ZGM—based on a zinc glycyrrhizinate microgel (ZGM) derived from the clinical anti‐inflammatory agent Licorzinc. This multifunctional gel encapsulates L. reuteri within a porous network, achieving a 23.08‐fold increase in survival rate under simulated gastric conditions and a 37.22‐fold increase in intestinal colonization in mice compared to unencapsulated bacteria. Beyond protection, ZGM actively scavenges ROS at inflammatory sites, facilitates probiotic adhesion to the mucus layer, and modulates the local microenvironment to favor colonization. In both dextran sulfate sodium (DSS)‐induced colitis and IL‐10‐deficient spontaneous colitis mouse models, L. reuteri@ZGM persistently scavenged ROS, effectively reduced pro‐inflammatory cytokine levels, restored the expression of tight junction‐associated proteins and intestinal barrier function, enhanced probiotic colonization and survival, and reshaped the gut microbiota. These findings establish L. reuteri@ZGM as a potent therapeutic strategy that integrates microenvironment modulation and probiotic delivery—offering a clinically translatable approach to treating inflammatory bowel diseases.
Meng-Yun Peng, Xiao-Chun Chen, Wei Li et al.· Advancement of science· 0 citations
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