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Sooty mould (SM) disease affects the growth, development and metabolism of plants and reduces the commodity and economic value of crops. SM disease is one of the important leaf diseases in tea plants. Nonetheless, studies on the effect of SM disease in tea plants are rare. Herein, we found that SM disease disrupted the cell morphology and structure and reduced the contents of caffeine, theanine, and catechins in the mature leaves of tea plants. Transcriptome analysis revealed that SM disease inhibited the biosynthesis of lignin, chlorophyll, catechin, caffeine, and theanine and affected the plant-pathogen interactions in the mature leaves of tea plants by downregulating gene expression. In addition, two fungal isolates, MTzyqA and MTzyqB, were obtained from the mature leaves of diseased tea plants. These strains were identified as Cladosporium pseudocladosporioides by mulitgene phylogenetic analysis, and they grew epiphytically on the leaves of tea plants. The biocontrol bacteria JT68, ZGT5, and BX1 had obvious inhibitory effect on MTzyqA and MTzyqB. These results provide a basis for understanding the effect of SM disease in tea plants. [ABSTRACT FROM AUTHOR]

As a rich green energy source, natural gas is widely used in many fields such as the chemical industry, automobile energy, and daily life. However, it is very challenging to separate and recover C2H6 and C3H8 from natural gas. Metal–organic frameworks (MOFs) as an emerging type of multi-pore porous materials show huge potential in gas adsorption separation. Herein, we report pillar-layered MOFs, Ni (BDC)(DABCO)0.5 (DMOF-X), modified by halogen atoms (F, Cl, Br), and investigate their CH4/C2H6/C3H8 separation performance. The experimental results show that DMOF-Cl exhibited a extremely high adsorption capacity for C3H8 and C2H6. Under the conditions of 298 K and 100 kPa, the adsorption capacities for C3H8 and C2H6 on DMOF-Cl are as high as 6.23 and 4.94 mmol g−1, which are superior to the values for most of the porous materials that have been reported. In addition, DMOF-Cl also shows high C3H8/CH4 (5: 85, V/V) and C2H6/CH4 (10: 85, V/V) separation selectivities, with values of 130.9 and 12.5, respectively. Finally, DMOF-Cl also demonstrated great potential as an adsorbent for separating C3H8/C2H6/CH4. [ABSTRACT FROM AUTHOR]

Developing hydrogen‐bonded organic frameworks (HOFs) that combine functional sites, size control, and storage capability for targeting gas molecule capture is a novel and challenging venture. However, there is a lack of effective strategies to tune the hydrogen‐bonded network to achieve high‐performance HOFs. Here, a series of HOFs termed as HOF‐ZSTU‐M (M=1, 2, and 3) with different pore structures are obtained by introducing structure‐directing agents (SDAs) into the hydrogen‐bonding network of tetrakis (4‐carboxyphenyl) porphyrin (TCPP). These HOFs have distinct space configurations with pore channels ranging from discrete to continuous multi‐dimensional. Single‐crystal X‐ray diffraction (SCXRD) analysis reveals a rare diversity of hydrogen‐bonding models dominated by SDAs. HOF‐ZSTU‐2, which forms a strong layered hydrogen‐bonding network with ammonium (NH4+) through multiple carboxyl groups, has a suitable 1D "pearl‐chain" channel for the selective capture of propylene (C3H6). At 298 K and 1 bar, the C3H6 storage density of HOF‐ZSTU‐2 reaches 0.6 kg L−1, representing one of the best C3H6 storage materials, while offering a propylene/propane (C3H6/C3H8) selectivity of 12.2. Theoretical calculations and in situ SCXRD provide a detailed analysis of the binding strength of C3H6 at different locations in the pearl‐chain channel. Dynamic breakthrough tests confirm that HOF‐ZSTU‐2 can effectively separate C3H6 from multi‐mixtures. [ABSTRACT FROM AUTHOR]

Brucellosis is a worldwide zoonosis. Vaccination is the most efficient means to prevent and control brucellosis. The current licensed attenuated vaccines for animal use were developed by sequential passage in non-natural hosts that decreased virulence in its original hosts. The attenuation mechanism of these strains remains largely unknown. In the present study, we sequenced the genome of Brucella melitensis vaccine strain M5-10. Sequence analysis showed that a large number of genetic changes occurred in the vaccine strains. A total of 2854 genetic polymorphic sites, including 2548 SNP, 241 INDEL and 65 MNV were identified. Of the 2074 SNPs in coding regions, 1310 (63.2%) were non-synonymous SNPs. Gene number, percent and N/S ratios were disproportionally distributed among the cog categories. Genetic polymorphic sites were identified in genes of the virB operon, flagella synthesis, and virulence regulating systems. These data indicate that changes in some cog categories and virulence genes might result in the attenuation. These attenuation mechanisms also have implications for screening and development of new vaccine strains. The genetic changes in the genome represent candidate sites for differential diagnosis between these vaccine strains and other virulence ones. Transcription analysis of virulence genes showed that expression of dnaK, vjbR were reduced in M5-10 strain when compared with that in 16M. A duplex PCR targeting virB6 and dnaK was successfully used to differentiate between M5-10 and the virulent 16M strain. The genome re-sequencing technique represents a strong strategy not only for evaluation of vaccines, but also for development of new vaccines.

Voltage-gated sodium (NaV) channels play fundamental roles in initiating and propagating action potentials. NaV1.3 is involved in numerous physiological processes including neuronal development, hormone secretion and pain perception. Here we report structures of human NaV1.3/β1/β2 in complex with clinically-used drug bulleyaconitine A and selective antagonist ICA121431. Bulleyaconitine A is located around domain I-II fenestration, providing the detailed view of the site-2 neurotoxin binding site. It partially blocks ion path and expands the pore-lining helices, elucidating how the bulleyaconitine A reduces peak amplitude but improves channel open probability. In contrast, ICA121431 preferentially binds to activated domain IV voltage-sensor, consequently strengthens the Ile-Phe-Met motif binding to its receptor site, stabilizes the channel in inactivated state, revealing an allosterically inhibitory mechanism of NaV channels. Our results provide structural details of distinct small-molecular modulators binding sites, elucidate molecular mechanisms of their action on NaV channels and pave a way for subtype-selective therapeutic development. NaV1.3 is involved in neuronal development, hormone secretion and pain perception. Here, the authors elucidate the molecular mechanism for modulation of NaV1.3 by a site-2 neurotoxin bulleyaconitine A and a subtype selective antagonist ICA121431. [ABSTRACT FROM AUTHOR]

Objective: To improve the awareness of immunodeficiency tuberculosis., Methods: 5 autopsy cases of immunodeficiency tuberculosis from 1972 to 2000 in two hospitals were reviewed., Results: The 5 cases were found to have hypoplasia of or damage in the thymus, among them 3 had massive tuberculous lymphadenitis lesions. Multiorgan lesions were found more in both lungs than in other organs, accompanied by lymphatic spread and blood dissemination. The microscopic feature was atypical tuberculosis with great amounts of Mycobacterium tuberculosis., Conclusions: Hypoplasia of or damage in the thymus and peripheral lymphoid tissue caused deficiency in the immune response, which resulted in the death of the patients with generalised tuberculosis by blood dissemination and lymphatic spread. The underlying mechanism of immunodeficiency tuberculosis is largely unknown, and further research is needed.