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In this study, for the environmental development, the antifungal, antibacterial, and antioxidant activities of a water extract of flowers from Acacia saligna (Labill.) H. L. Wendl. were evaluated. The extract concentrations were prepared by dissolving them in 10% DMSO. Wood samples of Melia azedarach were treated with water extract, and the antifungal activity was examined at concentrations of 0%, 1%, 2%, and 3% against three mold fungi; Fusarium culmorum MH352452, Rhizoctonia solani MH352450, and Penicillium chrysogenum MH352451 that cause root rot, cankers, and green fruit rot, respectively, isolated from infected Citrus sinensis L. Antibacterial evaluation of the extract was assayed against four phytopathogenic bacteria, including Agrobacterium tumefaciens, Enterobacter cloacae, Erwinia amylovora, and Pectobacterium carotovorum subsp. carotovorum, using the micro-dilution method to determine the minimum inhibitory concentrations (MICs). Further, the antioxidant capacity of the water extract was measured via 2,2′-diphenylpicrylhydrazyl (DPPH). Phenolic and flavonoid compounds in the water extract were analyzed using HPLC: benzoic acid, caffeine, and o-coumaric acid were the most abundant phenolic compounds; while the flavonoid compounds naringenin, quercetin, and kaempferol were identified compared with the standard flavonoid compounds. The antioxidant activity of the water extract in terms of IC50 was considered weak (463.71 μg/mL) compared to the standard used, butylated hydroxytoluene (BHT) (6.26 μg/mL). The MIC values were 200, 300, 300, and 100 µg/mL against the growth of A. tumefaciens, E. cloacae, E. amylovora, and P. carotovorum subsp. carotovorum, respectively, which were lower than the positive control used (Tobramycin 10 μg/disc). By increasing the extract concentration, the percentage inhibition of fungal mycelial was significantly increased compared to the control treatment, especially against P. chrysogenum, suggesting that the use of A. saligna flower extract as an environmentally friendly wood bio-preservative inhibited the growth of molds that cause discoloration of wood and wood products.

This study aimed to investigate the effect of sunflower seeds, either as whole or as oil, on rumen fermentation, milk production, milk composition and fatty acids profile in dairy goats. Fifteen lactating Damascus goats were divided randomly into three groups (n = 5) fed a basal diet of concentrate feed mixture and fresh Trifolium alexandrinum at 50:50 on dry matter basis (Control) in addition to 50 g/head/d sunflower seeds whole (SS) or 20 mL/head/d sunflower seeds oil (SO) in a complete randomized design. Milk was sampled every two weeks during 90 days of experimental period for chemical analysis and rumen was sampled at 30, 60, and 90 days of the experiment for ruminal pH, volatile fatty acids (tVFA), and ammonia-N determination. Addition of SO decreased (p = 0.017) ruminal pH, whereas SO and SS increased tVFA (p<0.001) and acetate (p = 0.034) concentrations. Serum glucose increased (p = 0.013) in SO and SS goats vs Control. The SO and SS treated goats had improved milk yield (p = 0.007) and milk fat content (p = 0.002). Moreover, SO increased milk lactose content (p = 0.048) and feed efficiency (p = 0.046) compared to Control. Both of SS and SO increased (p<0.05) milk unsaturated fatty acids content specially conjugated linolenic acid (CLA) vs Control. Addition of SS and SO increased (p = 0. 021) C18:3N3 fatty acid compared to Control diet. Data suggested that addition of either SS or SO to lactating goats ration had beneficial effects on milk yield and milk composition with enhancing milk content of healthy fatty acids (CLA and omega 3), without detrimental effects on animal performance.

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The objective of this study was to evaluate the effects of Saccharomyces cerevisiae on in vitro gas production (GP) kinetics and degradability of corn stover, oat straw, sugarcane bagasse and sorghum straw. Feedstuffs were incubated with different doses of yeast [0, 4, 8 and 12 mg/g dry matter (DM)] at direct addition or 72 h pre-incubation. Rumen GP was recorded at 2, 4, 6, 8, 10, 12, 14, 24, 30, 48, 54 and 72 h of incubation. After 72 h, rumen pH and methane were determined and contents were filtrated for DM, neutral (NDF) and acid detergent fibre (ADF) degradability. Fibrous species×method of application×yeast interactions occurred (P<0.001) for all measured ruminal GP parameters and degradability. The direct addition or 72 h pre-incubation of S. cerevisiae with corn stover improved (P<0.05) GP and methane and decreased (P<0.05) the lag time (L) and NDF degradability (NDFD). The direct addition of S. cerevisiae to oat straw increased (P<0.05) rate of GP (c) and decreased (P<0.05) asymptotic GP (b). However, 72 h pre-incubation increased (P<0.05) c with linearly decreased b, DM degradability (DMD) and NDFD. Applying S.cerevisiae for 72 h pre-incubation decreased (P<0.001) methane emission. The direct addition or 72 h pre-incubation of S. cerevisiae to sorghum straw increased (P<0.05) b, c, L, DMD and NDFD. Overall, the effect of dose varied among different feedstuffs and different application methods. Results suggested that the direct addition of S. cerevisiae could support and improve ruminal fermentation of lowquality forages at 4 to 12 g/kg DM.

This study determined the chemical composition and metabolizable energy (ME) value for ruminants of seeds and pulps from grape pomaces (GP), which were produced from white and red Vitis vinifera cultivars in Italy and California (USA). Six Italian (i.e., three white and three red) and five California red cultivars were collected after the crush of grape juice had been completed and were ensiled in micro-silos for 45 d. Fresh and ensiled samples were manually sieved to separate seeds from the pulp plus skin fraction and an overall inventory of 44 samples was obtained from the 24 Italian and 20 California samples (i.e., seeds and pulp fractions, fresh or ensiled from 6 or 5 cultivars, respectively). Both in seeds and pulp, the red Italian samples had higher organic matter (P<0.01), ether extract (P<0.05), neutral detergent fiber (aNDF, P<0.01), acid detergent fiber (ADF, P<0.01), lignin(sa, P<0.01) and Cu (P=0.02 and P<0.01, respectively) relative to the California red samples. In addition, K (P<0.01), Fe (P<0.01) and Zn (P=0.03 and P<0.01, respectively in seeds and pulps) were higher in red samples from California versus those from Italy. Italian white samples had higher saponins in pulp (SAP, P<0.05) and tended to have higher total extractable phenolics both in seeds and pulps (P=0.07 and P=0.10, respectively) than did Italian reds. Both in seeds and pulps, ensiling increased concentrations of aNDF (P<0.01 and P=0.08, respectively), ADF (P<0.01) and lignin(sa) (P<0.01 and P=0.03, respectively), had no impact on mineral levels and decreased concentrations anthocyanins (P=0.05) and SAP (P=0.01), respectively in seeds and pulp. Samples were fermented in diluted rumen fluid to measure in vitro rumen fermentability in terms of gas production, which was used to predict ME. Gas production from seeds of different origin were similar, with the exception of higher values at 48 h in red California cultivars with respect to those from Italy (19.2 ml versus 18.0 ml, P<0.05). In pulps, Italian reds did not differ from Italian whites, but had lower gas production than the red California samples (9.2 ml versus 12.2 ml, 16.6 ml versus 21.3 ml, 26.3 versus 32.7, P<0.01, at 4, 24 and 48 h respectively). Ensiling reduced gas production in seeds at 24 and 48 h of incubation (P<0.01) and in pulps at 48 h (P=0.09). Seeds from Italian red samples were lower (P<0.01) in ME than Italian whites (6.23 MJ/kg DM versus 6.89 MJ/kg DM, P<0.01) and higher (P<0.01) than the California samples (5.58 MJ/kg DM). There were no differences between ME of the groups of pulps, but ensiling reduced estimated ME content in seeds (5.94 MJ/kg DM versus 6.54 MJ/kg DM, P<0.01), but not in pulps. On the basis of our results, and in agreement with other recent papers and/or textbook data, the potential to use de-seeded GP as a feed in diets of high producing ruminants is limited

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