In this study, water extracts from fermented (F), ultrasonicated (US), and enzyme-hydrolyzed (E) rice bran (RB) were evaluated against sixteen fungal plant stem and root-rot-associated pathogens. The effects of pre-treated RB additives on plant growth substrate (PGS) on bean and tomato seed germination, stem height and root length of seedlings, and chlorophyll concentration in plants were analyzed. The results showed that US-assisted pre-treatments did not affect protein content in RB, while 36 h semi-solid fermentation (SSF) reduced protein content by 10.3–14.8%. US initiated a 2.9- and 2-fold increase in total sugar and total phenolics (TPC) contents compared to the untreated RB (3.89 g/100 g dw and 0.61 mg GAE/g dw, respectively). Lactic acid (19.66–23.42 g/100 g dw), acetic acid (10.54–14.24 g/100g dw), propionic acid (0.40–1.72 g/100 g dw), phenolic compounds (0.82–1.04 mg GAE/g dw), among which phenolic acids, such as p-coumaric, cinnamic, sinapic, vanillic, and ferulic, were detected in the fermented RB. The RB_F extracts showed the greatest growth-inhibition effect against soil-born plant pathogens, such as Fusarium, Pythium, Sclerotinia, Aspergillus, Pseudomonas, and Verticillium. Beans and tomatoes grown in RB_US+E- and RB_F-supplemented PGS increased the germination rate (14–75%), root length (21–44%), and stem height (25–47%) compared to seedlings grown in PGS. The RB additives increased up to 44.6–48.8% of the chlorophyll content in both plants grown under greenhouse conditions. The results indicate that the biological potential of rice-milling waste as a plant-growth-promoting substrate component can be enhanced using solid-state fermentation with antimicrobial LABs and US processing.

In this study, the influence of genotype, concentration of thidiazuron (TDZ), and explant position on the culture medium in organogenesis in a somatic tissue culture of two gloxinia cultivars was investigated. Isolated explants cultured on the medium containing TDZ formed adventitious shoots directly without an intervening callus phase. Explant regeneration frequency varied depending on the genotype, TDZ concentration, and explant position on the medium. The analysis of variance revealed that cultivar (C), TDZ concentration (T), position of explant on culture medium (P), and the interaction of C × T, C × P, T × P, and C × T × P significantly influenced the frequency of shoot formation. However, the effect of interface C × P and C × T × P on the number of shoots per explant was not significant. “Snowy” leaf explants manifested a significantly higher mean shoot formation frequency (p ˂ 0.01) in comparison with the cultivar “Midnight Purple”. The medium enriched with 3.5 μM TDZ resulted in the highest organogenesis frequency, while the highest shoot number per explant was acquired on medium supplemented with 4.0 μM TDZ. The explants of the tested cultivars cultured on the medium with the adaxial side down showed a significantly higher (p ˂ 0.01) shoot formation frequency in comparison with explants cultured on the medium with the abaxial side, and they showed a higher mean number of shoots per explant. An effective method for in vitro organogenesis of Sinningia speciosa (Lodd.) Hiern without an intervening callus phase was established.