Characteristics of nutrients in two dominant plant species and rhizospheric soils in alpine desert of the Qinghai-Xizang Plateau under contrasting climates北大核心CSCD

Aims This study was conducted to determine the responses of nutrients in plants and rhizospheric soils to climate in alpine-cold desert on the Qinghai-Xizang Plateau. Methods Tissue samples for two dominant plant species, Hippophae rhamnoides subsp. sinensis and Artemisia desertorum, and associated rhizospheric soil samples were collected from sites representing semi-Arid and sub-humid climates in the alpine-cold desert on the Qinghai-Xizang Plateau. Measurements were made on the contents of carbon, nitrogen and phosphorus in roots and shoots, as well as on organic carbon, total nitrogen, total phosphate, ammonium nitrogen, nitrate nitrogen and available phosphate in rhizospheric soils in the 0-10 cm and 10-20 cm layer. The relationship between nutrients in plant tissues and rhizospheric soils and the influencing factors were analyzed. Important findings There were significant differences between the semi-Arid and the sub-humid sites in tissue nutrients and rhizospheric soil nutrients for the two specie. Specifically, the contents of carbon, nitrogen, phosphorus in plant tissues differed significantly between the semi-Arid and the sub-humid sites. Soil organic carbon, total nitrogen, ammonium nitrogen, nitrate nitrogen and available phosphate for the rhizosphere of A. desertorum were significantly higher on site under sub-humid climate than that under semi-Arid climate; whereas the trend was reversed for the rhizosphere of H. rhamnoides subsp. sinensis. We found significant relationships between the tissue nutrients and soil nutrients, and significantly different plant nutrient ratios between the two species. There were negative correlations between tissues and rhizosheric soils in N:P ratio for A. desertorum and C:N ratio for H. rhamnoides subsp. sinensis under different climates. © 2018 Editorial Office of Chinese Journal of Plant Ecology. All rights reserved.     

大蒜根系分泌物的化感作用

以苍山白蒜和蔡家坡紫蒜为材料,采用水培方法收集根系分泌物,研究了2个大蒜品种的根系分泌物对莴苣种子发芽和幼苗生长及对黄瓜枯萎病菌、西瓜枯萎病菌的化感效应.结果表明:2个大蒜品种的根系分泌物对莴苣种子发芽和幼苗生长均表现为低浓度(0.1、0.2 g·mL-1)促进、高浓度(0.4、0.6 g·mL-1)抑制,高浓度时蔡家坡紫蒜的抑制作用大于苍山白蒜;对黄瓜枯萎病菌和西瓜枯萎病菌的菌丝生长及孢子萌发均表现为抑制作用,随着根系分泌物浓度的提高,抑制作用增强,其中黄瓜枯萎病菌较敏感,且蔡家坡紫蒜的抑制作用大于苍山白蒜.     

Requirements for mouse mammary tumor virus Rem signal peptide processing and function

Mouse mammary tumor virus (MMTV) encodes a Rev-like protein, Rem, which is involved in the nuclear export and expression of viral RNA. Previous data have shown that all Rev-like functions are localized to the 98-amino-acid signal peptide (SP) at the N terminus of MMTV Rem or envelope proteins. MMTV-SP uses endoplasmic reticulum-associated degradation (ERAD) for protein trafficking. Rem cleavage by signal peptidase in the ER is necessary for MMTV-SP function in a reporter assay, but many requirements for trafficking are not known. To allow detection and localization of both MMTV-SP and the C-terminal cleavage product, we prepared plasmids expressing green fluorescent protein (GFP) tags. N-terminal Rem tagging led to protein accumulation relative to untagged Rem and allowed signal peptidase cleavage but reduced its specific activity. C-terminal tagging also led to Rem accumulation yet dramatically reduced cleavage, GFP fluorescence, and activity relative to N-terminally tagged Rem (GFPRem). Substitutions of an invariant leucine at position 71 between the known RNA-binding and nuclear export sequences interfered with GFPRem accumulation and activity but not cleavage. Similarly, deletion of 100 or 150 C-terminal amino acids from GFPRem dramatically reduced both Rem and MMTV-SP levels and function. Removal of the entire C terminus (203 amino acids) restored both protein levels and activity of MMTV-SP. Only C-terminal GFP tagging, and not other modifications, appeared to trap Rem in the ER membrane. Thus, Rem conformation in both the ER lumen and cytoplasm determines cleavage, retrotranslocation, and MMTV-SP function. These mutants further characterize intermediates in Rem trafficking and have implications for all proteins affected by ERAD.     

一株产纤维素酶细菌的分离鉴定及酶学特性研究

从采集的含腐烂树叶的土壤中,筛选到1株产纤维素酶能力较高的菌株JJ-3,经16S r RNA基因序列分析,鉴定该菌株为产酸克雷伯氏杆菌(Klebsiella oxytoca)。产酶条件及酶学特性研究表明:以滤纸为碳源、蛋白胨为氮源、初始p H为8.0的培养基中发酵3 d更利于纤维素酶的合成;菌株发酵液在中性和碱性条件下均有较高的滤纸酶活力,分别可达118.7 U/m L(p H7.0),167.8 U/m L(p H8.0)和120 U/m L(p H9.0);所产纤维素酶的最适酶反应p H为7.0,最适酶反应温度为40℃,对温度比较敏感,在p H7.0-8.0的范围内具有较好的稳定性,能满足中性和碱性纤维素酶的要求。     

马槟榔甜蛋白基因(MBLⅡ)的拼接与表达载体的构建

从云南植物Capparismasaikai中提取总DNA,设计引物克隆马槟榔甜蛋白基因MBLⅡ,序列测定后经同源性分析表明与GeneBank中登陆的马槟榔甜蛋白基因MBLⅡ(cDNA)序列一致,表明MBLⅡ不存在内含子序列。利用重叠区扩增基因拼接法(genesplicingbyoverlapextension,geneSOEing)进行体外基因剪接,剪接片段与植物表达载体pVKH相连,构建pVKH-35S-MBLⅡ-Pa、pVKH-35S-S-A B-pA、pVKH-35S-A B-pA、pVKH-35S-S-A-pA、pVKH-35S-S-B-pA,为寻找mabinlin的活性表达形式和翻译后剪接机制打下基础。     

A study of the genetic polymorphism of human inter-alpha-trypsin-inhibitor (ITI) in the Han population,Chengdu, China

Phenotypes of inter-alpha-trypsin-inhibitor (ITI) have been determined by isoelectric focusing on polyacrylamide gels followed by immunofixation. The phenotype frequencies of ITI in the Han population in Chengdu, P. R. China have been investigated using this method. In addition, family studies have been conducted in 21 families. The results show that ITI is polymorphic in the Han population in Chengdu, China. The allele frequencies are as follows: ITI*1 = 0.5763. ITI*2 = 0.4107, ITI*3 = 0.0130. ITI is thus a new and promising genetic marker that can be used in the field of forensic haematogenetics.     

Ar + H<Subscript>2</Subscript> Plasma Interacting with Lithium-Filled Capillary Porous Structure

Ar + H₂ plasma interacting with liquid lithium was carried out on a one-cathode linear plasma device (SCU-PSI). The lithium sample was covered with capillary porous structure (CPS). It is found that the electron temperature of applied plasma ranged from ~0–1 eV and electron density ranged from 0.1 × 10²⁰ to 1 × 10²⁰ m^?3. The experimental results indicate that a reduction in the electron temperature and the lithium evaporation is found as the percentage of H₂ increases When the ratio of argon and hydrogen keeps constant, the electron temperature and lithium evaporation increase with applied input power, respectively. The retention of hydrogen atoms in lithium surface results in reducing the lithium evaporation. The XRD analysis result shows that during plasma radiation no LiH is formed.     

Proteomic analysis of buccal gland secretion from fasting and feeding lampreys (<Emphasis Type="Italic">Lampetra morii</Emphasis>)

Background

Previous studies have shown that lamprey buccal glands contain some regulators related to anticoagulation, nociception, and immune responses due to the blood sucking habit. Regrettably, the protein expression profile in the buccal glands of feeding lampreys has never been reported yet. The present study was performed in order to further identify more proteins which are closely associated with lamprey feeding process.

Methods

2D-PAGE, NanoLC–MS/MS with higher resolution, Ensembl lamprey and NCBI protein databases, as well as western blot was used to compare the proteomics of buccal gland secretion from China northeast lampreys (Lampetra morii) which had been fed for 0, 10, and 60 min, respectively.

Results

In the present study, the number of identified protein species in the buccal glands of feeding groups (60 min) was increased significantly, nearly ten times of that in the fasting group. During the feeding stage, novel proteins emerged in the buccal gland secretion of lampreys. According to gene ontology (GO) analysis and function predictions, these proteins were summarized and discussed based on their potential roles during feeding process. Furthermore, some of the identified proteins were confirmed to express during the feeding time of lampreys.

Conclusion

When lampreys attack host fishes to suck blood and flesh, their buccal glands could secrete enough proteins to suppress blood coagulation, nociception, oxidative stress, immune response, as well as other adverse effects encountered during their parasitic lives. The present study would provide clues to clarify the feeding mechanism of the bloodsucking lampreys.

     

A novel pro-apoptosis protein PNAS-4 from <Emphasis Type="Italic">Xenopus laevis</Emphasis>: Cloning,expression, purification,and polyclonal antibody production

Human PNAS-4 was identified as a novel pro-apoptotic protein in mammalian cells. Here we report the cloning, expression, purification, and antibody production of a PNAS-4 homolog (named xPNAS-4) from Xenopus laevis, an extensively used model organism in exploring gene functions during embryonic development. Recombinant histidine-tagged xPNAS-4 protein was expressed in Escherichia coli as insoluble inclusion bodies. The inclusion bodies were subsequently dissolved in 8 M urea and purified to near homogeneity by Ni2+ affinity chromatography. The resulting denatured protein was refolded by stepwise dilution of urea concentration via dialysis. This procedure yielded about 4 mg refolded protein per liter of E. coli culture with a purity of 95%. The purified protein was identified by liquid chromatography-electrospray ionization-quadrupole-time of flight-mass spectrometry (LC-ESI-Q-TOF-MS) and used to raise anti-xPNAS-4 polyclonal antibodies that were suitable for detecting the expression of PNAS-4 in X. laevis embryos by Western blotting. The availability of recombinant protein and specific polyclonal antibodies will provide a valuable tool in studying apoptotic mechanisms of this protein. To our knowledge, this is the first report to demonstrate the presence of PNAS-4 in X. laevis.