整合分析氮磷添加对土壤酶活性的影响

本文通过整合分析(Meta-analysis)的方法分析了氮、磷添加对土壤碳、氮和磷素循环水解酶以及土壤氧化酶活性的影响.结果表明: 氮添加显著增加了碳、氮和磷循环水解酶的活性,增幅分别为6.9%、5.6%和10.7%;与氮添加相比,在氮磷同时添加下,3类土壤酶的活性增加更为显著,增幅分别达13.4%、37.4%和13.3%.然而,对于土壤氧化酶,氮以及氮磷的添加都使其活性降低,分别降低了6.1%和0.4%.不同生态系统类型、氮肥类型、施肥速率和施肥试验时间都对土壤酶活性具有影响.在全球大气氮沉降与磷添加逐渐增加的背景下,土壤微生物活性和酶的变化将会对土壤生物地球化学循环过程和土壤生态系统功能产生重要影响.     

庙岛群岛典型植物群落物种、功能、结构多样性及其对环境因子的响应

海岛植被在全球生物多样性研究中起重要作用,研究海岛植被多样性对于理解海陆相互作用下植物群落的多样性维持机制有重要意义.本研究以庙岛群岛的麻栎群落、刺槐群落、黑松群落、荆条群落4种典型植物群落为对象,采用物种多样性指数、功能多样性指数和结构多样性指数,在群落尺度上探讨了海岛典型植物群落物种、功能、结构多样性间的关系及其对环境因子的响应.结果表明: 黑松群落的物种丰富度与Rao指数高于刺槐群落与麻栎群落,而结构多样性却较低;荆条灌丛的物种、结构多样性均低于森林群落,而功能多样性高于部分森林群落.物种丰富度与Rao指数以及树高多样性间呈显著正相关,与功能均匀度呈显著负相关.结构多样性主要由坡度决定且与坡度呈负相关;功能均匀度与坡度呈正相关,而功能异质性、功能离散度和物种多样性则更多地受土壤理化性质的影响,与土壤容重及土壤总碳呈正相关,与土壤含水率呈负相关.总体而言,庙岛群岛的植物群落多样性格局既有与大陆植被相似的特征,但也有其海岛特殊性.     

黔产莪术油的品质分析

该研究应用比重瓶法、折光率测定法、旋光度测法及电感耦合等离子体发射光谱法,分别对莪术油的相对密度、折光率、比旋度、重金属含量进行了测定,同时采用HPLC法测定莪术油中成分含量以及建立指纹图谱进行相似度的比较分析。结果表明:黔产莪术油的相对密度为0.987 0,比旋度为+24.146 8°,折光率为1.509,指纹图谱与中药制剂指纹图谱对照,相似度为0.976,总重金属含量总和10 mg·kg~(-1),砷盐未检测出。检测的各项指标均符合2015版中国药典莪术油项下的相关规定,该研究方法可行、数据可靠。该研究结果确认了黔产莪术油有较高的安全性及良好的品质,可作为药材原料使用,为黔产莪术油的综合开发利用及质量控制提供了科学依据。     

Compatibility of Molybdenum,Tungsten, and 304 Stainless Steel in Static Liquid Lithium Under High Vacuum

Molybdenum (Mo), tungsten (W), and stainless steel (SS) are widely used as important structure materials and first wall materials in fusion devices, while liquid lithium (Li) limiter/divertor can provide an attractive option for withstanding high heat load and solving life-time problem of first wall. Studying the compatibility of these materials exposed to liquid Li is significant for the application in Mo, W, and SS in fusion reactors. The corrosion behaviors of Mo, W, and 304SS exposed to static liquid Li at 600 K up to 1320 h under high vacuum with pressure 10^?4 Pa were investigated. After exposure to liquid Li, it was found that the weight loss of Mo, W, and 304SS increases with corrosion time, but the total amount is moderate. 304SS specimens produce a non-uniform corrosion behavior because of Cr, Ni, and carbon (C) elements selectivity depletion and formation of carbides compound near surface. Mo and W surface microstructures are unchanged. 304SS surface hardness increases with corrosion products because these particles include C element, which increases by 49 HV after exposed to liquid Li for 1320 h, while Mo and W surface hardness are unchanged by the reason of their excellent corrosion resistance.     

SIRT1 mediates salidroside‐elicited protective effects against MPP+‐induced apoptosis and oxidative stress in SH‐SY5Y cells: involvement in suppressing MAPK pathways

Parkinson's disease (PD) is a progressive neurodegenerative disease, leading to tremor, rigidity, bradykinesia, and gait impairment. Salidroside has been reported to exhibit antioxidative and neuroprotective properties in PD. However, the underlying neuroprotective mechanisms effects of salidroside are poorly understood. Recently, a growing body of evidences suggest that silent information regulator 1 (SIRT1) plays important roles in the pathophysiology of PD. Hence, the present study investigated the roles of SIRT1 in neuroprotective effect of salidroside against N‐methyl‐4‐phenylpyridinium (MPP⁺)‐induced SH‐SY5Y cell injury. Our findings revealed that salidroside attenuates MPP⁺‐induced neurotoxicity as evidenced by the increase in cell viability, and the decreases in the caspase‐3 activity and apoptosis ratio. Simultaneously, salidroside pretreatment remarkably increased SIRT1 activity, SIRT1 mRNA and protein levels in MPP⁺‐treated SH‐SY5Y cell. However, sirtinol, a SIRT1 activation inhibitor, significantly blocked the inhibitory effects of salidroside on MPP⁺‐induced cytotoxicity and apoptosis. In addition, salidroside abolished MPP⁺‐induced the production of reactive oxygen species (ROS), the up‐regulation of NADPH oxidase 2 (NOX2) expression, the down‐regulations of superoxide dismutase (SOD) activity and glutathione (GSH) level in SH‐SY5Y cells, while these effects were also blocked by sirtinol. Finally, we found that the inhibition of salidroside on MPP⁺‐induced phosphorylation of p38, extracellular signal‐regulated kinase (ERK) and c‐Jun NH2‐terminal kinase (JNK) were also reversed by sirtinol in SH‐SY5Y cells. Taken together, these results indicated that SIRT1 contributes to the neuroprotection of salidroside against MPP⁺‐induced apoptosis and oxidative stress, in part through suppressing of mitogen‐activated protein kinase (MAPK) pathways.     

A new xanthene‐based two‐photon fluorescent probe for the imaging of 1,4‐dithiothreitol (DTT) in living cells

1,4‐Dithiothreitol (DTT) has wide applications in cell biology and biochemistry. Development of effective methods for monitoring DTT in biological systems is important for the safe handling and study of toxicity to humans. Herein, we describe a two‐photon fluorescence probe (Rh‐DTT) to detect DTT in living systems for the first time. Rh‐DTT showed high selectivity and sensitivity to DTT. Rh‐DTT can be successfully used for the two‐photon imaging of DTT in living cells, and also can detect DTT in living tissues and mice.     

The effect of 7,8,4´‐trihydroxyflavone on tyrosinase activity and conformation: Spectroscopy and docking studies

Tyrosinase is a ubiquitous enzyme that plays an essential role in the production of melanin. Effective inhibitors of tyrosinase have extensive applications in the medical, cosmetic and food industries. In this study, a combination of enzyme kinetics, ultraviolet (UV)‐visible absorption, fluorescence spectroscopic techniques and a computational simulation method was used to characterize the inhibitory mechanism of 7,8,4´‐trihydroxyflavone on tyrosinase. 7,8,4´‐Trihydroxyflavone was found to strongly inhibit the oxidation of l ‐DOPA by tyrosinase with an IC₅₀ value of 10.31 ± 0.41 μM. The inhibitory mechanism was determined to be reversible and non‐competitive with a K_i of 9.50 ± 0.40 μM. The UV absorption spectra showed that 7,8,4´‐trihydroxyflavone could chelate with copper ions and form a complex with tyrosinase. The intrinsic fluorescence of tyrosinase was quenched by 7,8,4´‐trihydroxyflavone through a static quenching mechanism. 7,8,4´‐Trihydroxyflavone was found to occupy a single binding site with a binding constant of 7.50 ± 1.20 × 10⁴ M^?1 at 298 K. The conformation of tyrosinase changed, and the microenvironment became more hydrophilic after 7,8,4´‐trihydroxyflavone binding. Thermodynamics parameters indicated that the binding was a spontaneous process and involved hydrogen bonds and van der Waals forces. The binding distance was evaluated to be 4.54 ± 0.05 nm. Docking simulation analysis further authenticated that 7,8,4´‐trihydroxyflavone could form hydrogen bonds with the residues His244 and Met280 within the tyrosinase active site. Our results will contribute to further understanding of the inhibitory mechanisms of 7,8,4´‐trihydroxyflavone against tyrosinase and will facilitate future screening for tyrosinase inhibitors.     

Identification of a specific molecular marker for the rice blast-resistant gene <Emphasis Type="Italic">Pigm</Emphasis> and molecular breeding of thermo-sensitive genic male sterile leaf-color marker lines

Rice blast is a damaging disease caused by Magnaportheoryzae. Marker-assisted selection of blast resistance genes could help develop cultivars with blast resistance. Pigm is a broad-spectrum blast-resistant gene. However, few rice resources contain Pigm. In this study, the Pigm gene donor Gumei4 (GM4) was investigated. By analyzing different regions of Pigm sequences, we found that marker G8900 was a specific molecular marker of Pigm gene in GM4. Correlation analysis between molecular marker detection and identification of rice blast disease nursery revealed that G8900 could be used in marker-assisted selection (MAS) of Pigm. Furthermore, we introduced Pigm gene into the KT27S line (a blast-susceptible yellow-green-leaf-color mutant) in G8900-assisted breeding and identified three new yellow-green-leaf-color marker lines that are resistant to blast. The agronomic and economic traits of the three new lines are similar to those of their parental lines. The identification and application of Pigm-specific molecular marker in breeding of yellow-green-leaf-color marker line could play an important role in the production of disease-resistant hybrid rice.     

Identifying sequence features that drive ribosomal association for lncRNA

Background

With the increasing number of annotated long noncoding RNAs (lncRNAs) from the genome, researchers are continually updating their understanding of lncRNAs. Recently, thousands of lncRNAs have been reported to be associated with ribosomes in mammals. However, their biological functions or mechanisms are still unclear.

Results

In this study, we tried to investigate the sequence features involved in the ribosomal association of lncRNA. We have extracted ninety-nine sequence features corresponding to different biological mechanisms (i.e., RNA splicing, putative ORF, k-mer frequency, RNA modification, RNA secondary structure, and repeat element). An \(\mathcal {L}1\)-regularized logistic regression model was applied to screen these features. Finally, we obtained fifteen and nine important features for the ribosomal association of human and mouse lncRNAs, respectively.

Conclusion

To our knowledge, this is the first study to characterize ribosome-associated lncRNAs and ribosome-free lncRNAs from the perspective of sequence features. These sequence features that were identified in this study may shed light on the biological mechanism of the ribosomal association and provide important clues for functional analysis of lncRNAs.