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Background: Wall-associated kinase (WAK)/WAK-like (WAKL) is one of the subfamily of receptor like kinases (RLK). Although previous studies reported that WAK/WAKL played an important role in plant cell elongation, response to biotic and abiotic stresses, there are no systematic studies on RcWAK/RcWAKL in rose. Results: In this study, we identified a total of 68 RcWAK/RcWAKL gene family members within rose (Rosa chinensis) genome. The RcWAKs contained the extracellular galacturonan-binding domain and calcium-binding epidermal growth factor (EGF)-like domain, as well as an intracellular kinase domains. The RcWAKLs are missing either calcium-binding EGF-like domain or the galacturonan-binding domain in their extracellular region. The phylogenetic analysis showed the RcWAK/RcWAKL gene family has been divided into five groups, and these RcWAK/RcWAKL genes were unevenly distributed on the 7 chromosomes of rose. 12 of RcWAK/RcWAKL genes were significantly up-regulated by Botrytis cinerea-inoculated rose petals, where RcWAK4 was the most strongly expressed. Virus induced gene silencing of RcWAK4 increased the rose petal sensitivity to B. cinerea. The results indicated RcWAK4 is involved in the resistance of rose petal against B. cinerea. Conclusion: Our study provides useful information to further investigate the function of the RcWAK/RcWAKL gene family and breeding research for resistance to B. cinerea in rose. [ABSTRACT FROM AUTHOR]

• The Tb 2 O 3 /g-C 3 N 4 heterojunction composites were constructed. • The composites reveal excellent photo-degradation efficiency. • The Tb4+/Tb3+ redox center promote the charge carriers separation. • The yield of hydroxyl radical was increasing sharply. • The possible mechanism of material was systematically discussed. Recently, the issue of environmental pollution by wastewater containing dye molecules attracted researcher's attention. It is urgent that seeking high efficiency visible-light driven photocatalyst leads to mitigating environmental contamination. In this work, the novel Tb 2 O 3 /g-C 3 N 4 composite photocatalysts have been successfully synthesized, and the enhanced photocatalytic performance has been thoroughly discussed based on the fully characterization. The X-ray diffraction and scanning electron microscopy exhibited crystalline phases and morphologies of obtained samples. The chemical states and composition of composite photocatalysts were characterized by the X-ray photoelectron spectrometer. The photoluminescence and photocurrent results proved that Tb 2 O 3 /g-C 3 N 4 composite samples possessed higher separation efficiency than that of pure C 3 N 4. The decomposition of organic contaminant and cycle experiment demonstrated that 0.8%Tb 2 O 3 /g-C 3 N 4 composite photocatalyst possessed the best photo-degradation performance and had a good chemical stability. The trapping experiment illustrated that the significantly elevated photocatalytic performance could attribute to the loading of Tb 2 O 3. The in-built redox centers of Tb4+/Tb3+ efficiently promoted the utilization of photo-generated electrons and proliferated the hydroxyl radical. Simultaneously, the mechanism of enhanced photocatalytic performance of obtained composite samples was proposed. This work provides a promising strategy to design novel visible-light-driven photocatalysts and further improve the photocatalysis mechanism survey. The as-prepared Tb 2 O 3 /g-C 3 N 4 composite heterojunction semiconductor exhibited higher photocatalytic activity by degrading organic pollutant under visible light illumination and 0.8%Tb 2 O 3 /g-C 3 N 4 presented the best photo-degradation properties compare with other samples. The degradation efficiency of 0.8%Tb 2 O 3 /g-C 3 N 4 was 1.5 times higher than that of pure C 3 N 4. According to a series of experimental characteristic analysis, it proved that the heterojunction was successfully formed and the existence of Tb 2 O 3 dramatically improved photo-activity of C 3 N 4. The enhanced photocatalytic performance for Tb 2 O 3 /g-C 3 N 4 could be attributed to two aspects: (i) inhibit charge carriers recombination, (ii) the formation of redox center (Tb4+/Tb3+), raise yield of .OH. This work not only provides a thought of high efficiency visible-light-driven photocatalyst, but also further expounds mechanism of action. [Display omitted] [ABSTRACT FROM AUTHOR]

Key message: Rose has 19 MLO genes. Of these, RhMLO1 and RhMLO2 were shown to be required for powdery mildew infection, which suggests their potential as susceptibility targets towards disease resistance. Powdery mildew, caused by Podosphaera pannosa, is one of the most serious and widespread fungal diseases for roses, especially in greenhouse-grown cut roses. It has been shown that certain MLO genes are involved in powdery mildew susceptibility and that loss of function in these genes in various crops leads to broad-spectrum, long-lasting resistance against this fungal disease. For this reason, these MLO genes are called susceptibility genes. We carried out a genome-wide identification of the MLO gene family in the Rosa chinensis genome, and screened for allelic variants among 22 accessions from seven different Rosa species using re-sequencing and transcriptome data. We identified 19 MLO genes in rose, of which four are candidate genes for functional homologs in clade V, which is the clade containing all dicot MLO susceptibility genes. We detected a total of 198 different allelic variants in the set of Rosa species and accessions, corresponding to 5–15 different alleles for each of the genes. Some diploid Rosa species shared alleles with tetraploid rose cultivars, consistent with the notion that diploid species have contributed to the formation of tetraploid roses. Among the four RhMLO genes in clade V, we demonstrated using expression study, virus-induced gene silencing as well as transient RNAi silencing that two of them, RhMLO1 and RhMLO2, are required for infection by P. pannosa and suggest their potential as susceptibility targets for powdery mildew resistance breeding in rose. [ABSTRACT FROM AUTHOR]

Purpose:To systematically review available evidence of indirect comparisons from RCTs and direct comparisons from observational studies regarding the comparative effectiveness and safety of DOACs in patients with AF. Methods: Electronic databases including EMBASE, MEDLINE, and PUBMED were searched up to June 5th, 2020. Primary endpoints included effectiveness (stroke or systemic embolism [SE]) and safety (major bleeding) outcomes. Bucher methods and random-effects models were conducted for indirect and direct comparisons among DOACs, respectively. Ranking probability analyses and the number needed to treat for net effect (NNTnet) were applied. Results: A total of 36 studies, involving 7 RCTs (n = 60,292 patients) and 29 observational studies (n = 1,164,821 patients), were included for analyses. Regarding the risk of stroke/SE, no significant differences were found from indirect comparisons of RCTs among the DOACs. For major bleeding, apixaban tended to be safer than rivaroxaban and dabigatran based on both direct and indirect comparisons (all p < 0.05; evidence quality: very low to moderate). Ranking probability analysis showed that apixaban had a high probability of being the best treatment in decreased risk of stroke/SE and major bleeding (80.30% and 91.30%, respectively). Likewise, apixaban was found to have the highest net clinical benefit (0.02, 95% CI: 0.014–0.029) and smallest NNTnet (48, 95% CI: 35–74). Conclusions: Apixaban appeared to have a favorable effectiveness-safety profile compared with the other DOACs in AF for stroke prevention, based on evidence from both direct and indirect comparisons. However, additional high-quality evidence is needed to support firm recommendations on clinical decision-making. [ABSTRACT FROM AUTHOR]

This study was conducted to explore whether acute lymphoblastic leukemia (ALL)-derived exosomes affect natural killer (NK) cells. Exosomes were isolated and identified from Jurkat cells and co-cultured with NK cells. Then, the cytotoxicity, viability, and release of perforin and granzyme B in NK92-MI cells were measured. PCR arrays were used to detect gene expression alterations in the transforming growth factor (TGF)-β pathway of NK92-MI cells treated or not treated with exosomes. The morphology and size of the exosomes isolated from Jurkat cells showed typical characteristics of exosomes, and the expression of cluster of differentiation 63 was detected. Jurkat-derived exosomes were internalized by NK92-MI cells, further inhibiting the proliferation and cytotoxicity of NK92-MI cells. An enzyme-linked immunosorbent assay revealed that the release of perforin and granzyme B from NK92-MI cells decreased after co-culture with exosomes. Similarly, western blot and immunofluorescence staining verified that Jurkat-derived exosomes inhibited the expression of granzyme B and perforin. Furthermore, Jurkat-derived exosomes enhanced the signaling of the TGF-β pathway in NK92-MI cells via the MDS1 and EVI1 complex loci and homeodomain interacting protein kinase 2. In conclusion, we found that ALL-derived exosomes inhibit the biological function of NK cells and provide support for the immunotherapy of ALL. [ABSTRACT FROM AUTHOR]

A versatile metal- and base-free direct reductive amination of aldehydes with amines using formic acid as a reductant under the catalysis of inexpensive BF3·Et2O has been developed. A wide range of primary and secondary amines and diversely substituted aldehydes are compatible with this transformation, allowing facile access to various secondary and tertiary amines in high yields with wide functional group tolerance. Moreover, the method is convenient for the late-stage functionalization of bioactive compounds and preparation of commercialized drug molecules and biologically relevant N-heterocycles. The procedure has the advantages of simple operation and workup and easy scale-up, and does not require dry conditions, an inert atmosphere or a water scavenger. Mechanistic studies reveal the involvement of imine activation by BF3 and hydride transfer from formic acid. [ABSTRACT FROM AUTHOR]

Nisin is an antimicrobial peptide which is widely used as preservative, while lactic acid is a natural organic acid applied in the food industry. The aim of this work was to study the process for nisin and lactic acid production from starch of sweet potato with simultaneous saccharification and fermentation (SSF) by Lactococcus lactis subsp. Lactis with two stage pH adjustment. The factors impacting the nisin and lactic acid production including starch concentration, glucosidase concentration, CaCO3 and Tween-80 were studied. The nisin titre reached a high of 2516.41 IU/mL, while the lactic acid reached a high of 37.06 g/L when the optimal conditions were 40 g/L starch, 100 U glucosidase/g starch, 2.5% CaCO3 and 1 mL/L Tween-80. The lactic acid and nisin were separated by a two stage pH adjustment at last. The SSF of starch from sweet potato coupled with a two stage pH adjustment is a promising method to produce nisin and lactic acid. [ABSTRACT FROM AUTHOR]