模拟酸雨对3种果树的胁迫效应

以青梅(Prunus mume Sieb.&Zucc.)、龙眼(Dimocarpus longan Lour.)和杨桃(Averrvhoa carambola L.)3种南方果树为材料,研究不同pH值的模拟酸雨对其生理胁迫的效应.在酸雨胁迫下3种果树的叶片叶绿素含量均随pH值的降低有不同程度的下降,叶片伤害率、细胞质膜透性、脯氨酸及丙二醛(MDA)含量则随pH值的降低而上升.抗性较强的龙眼的生理生化指标的变幅最小,其次是杨桃,对酸雨胁迫反应较敏感的青梅变幅最大.     

大兴安岭北部林区野果资源及保护利用

调查了大兴安岭北部林区野生果树种质资源及其开发利用现状。记录到该地区野生肉果类10科,15属,29种。其中越桔和笃斯越桔是大兴安岭北部林区资源极其丰富的野果。蔷薇科有16种,为该地区野生果树的优势科。介绍了11种具有重要经济价值的野果。大兴安岭北部林区的野果资源已得到初步开发利用,越桔、笃斯越桔、山刺玫等数种野果已进入产业化阶段。提出了合理保护和利用对策。     

中条山野生葡萄产香酵母的筛选及其混菌发酵对葡萄酒香气成分的影响

【背景】产香酵母可赋予葡萄酒独特的香气,因此,分离筛选优良产香酵母对酿造具有地域风味的特色葡萄酒具有重要意义。【目的】从中条山野生葡萄中筛选产香酵母,进行种群鉴定和生理生化特性研究,并将其应用于葡萄酒发酵过程,研究其对葡萄酒香气成分的影响。【方法】采用稀释涂布平板法从中条山野葡萄中分离筛选酵母菌,对其进行分子生物学鉴定。优选其中具有显著香气的产香酵母,与酿酒酵母F15进行混合发酵,采用气相色谱质谱联用(gas chromatograph-mass spectrometer,GC-MS)对香气成分进行分析,采用半定量法测定香气成分含量。【结果】共分离获得各种菌株13株,26S rRNA基因D1/D2区序列分析表明它们分布于Issatchenkia、Torulaspora、Pichia、Saccharomyces和Rhodotorula等5个不同属内。优选其中一株香气较为浓郁的酵母菌株Issatchenkia orientalis strain XS-6开展研究,结果发现该菌株最高耐受乙醇浓度为8%,最高耐受NaCl浓度为6%,最适生长温度为38℃。与酿酒酵母F15混菌发酵的葡萄酒中共检测出31种香气成分。香气物质总含量较单菌发酵增加19.8%,其中11种香气成分含量增加明显,尤其是具有玫瑰香气的苯乙醇。醇类与酯类物质含量较单菌发酵增加19.6%,并发现了香草酸乙酯(ethyl vanillate)、邻苯二甲酸二丁酯(dibutyl phthalate)等7种新的酯类物质。【结论】产香酵母XS-6对乙醇、NaCl、温度等具有良好的耐受性,而且与酿酒酵母F15混菌发酵对西拉葡萄酒香气成分具有明显的影响,可能在改善葡萄酒风味方面具有潜在的应用价值。     

珍稀植物蒜头果野生植株结实量及果实特征研究

该研究对云南省广南县不同分布点的野生植株大小与结实量,果实、果核性状特征,果皮与果核性状间的关系进行了分析。结果表明:(1)野生成年植株个体间结实量差异大,单株结实量从几十个至几千个,变异系数可达136.38%。结实量与冠幅有正相关关系(R=0.592,P0.01),与胸径和树高无相关关系(P0.05)。(2)扁球型果实平均纵径37.10~40.36 mm,变异系数7.28%~8.65%;平均横径41.15~45.03mm,变异系数6.44%~9.31%;平均果实重量35.77~47.29 g,变异系数18.99%~21.44%。野生蒜头果果实大小差异明显,单个果实重量差别为3.4倍。(3)果核平均纵径27.50~31.69 mm,变异系数7.13%~10.99%;平均横径30.94~34.16 mm,变异系数6.47%~9.41%;平均果核重量14.03~18.77 g,变异系数17.37%~22.68%。单个果核重量差别为3.7倍。(4)平均果皮纵向厚度4.33~4.80 mm,变异系数20.22%~26.91%;平均横向厚度5.10~5.44 mm,变异系数12.92%~20.98%;平均果皮重21.62~28.51 g,变异系数20.01%~24.12%。该研究结果表明野生蒜头果单株结实量、果实和果核大小、果皮厚等表型性状存在广泛的多样性,其资源为人工定向培育和开发利用提供了较为丰富的选择材料。     

Effects of amount and recurrence of leaf herbivory on the induction of direct and indirect defences in wild cotton

• The induction of defences in response to herbivory is a key mechanism of plant resistance. While a number of studies have investigated the time course and magnitude of plant induction in response to a single event of herbivory, few have looked at the effects of recurrent herbivory. Furthermore, studies measuring the effects of the total amount and recurrence of herbivory on both direct and indirect plant defences are lacking. To address this gap, here we asked whether insect leaf herbivory induced changes in the amount and concentration of extrafloral nectar (an indirect defence) and concentration of leaf phenolic compounds (a direct defence) in wild cotton (Gossypium hirsutum).
• We conducted a greenhouse experiment where we tested single event or recurrent herbivory effects on defence induction by applying mechanical leaf damage and caterpillar (Spodoptera frugiperda) regurgitant.
• Single events of 25% and 50% leaf damage did not significantly influence extrafloral nectar production or concentration. Extrafloral nectar traits did, however, increase significantly relative to controls when plants were exposed to recurrent herbivory (two episodes of 25% damage). In contrast, phenolic compounds increased significantly in response to single events of  leaf damage but not to recurrent damage. In addition, we found. that local induction of extrafloral nectar production was stronger than systemic induction, whereas the reverse pattern was observed for phenolics.
• Together, these results reveal seemingly inverse patterns of induction of direct and indirect defences in response to herbivory in wild cotton.

     

Site-specific oxidation of apolipoprotein A-I impairs cholesterol export by ABCA1, a key cardioprotective function of HDL

The mechanisms that deprive HDL of its cardioprotective properties are poorly understood. One potential pathway involves oxidative damage of HDL proteins by myeloperoxidase (MPO) a heme enzyme secreted by human artery wall macrophages. Mass spectrometric analysis demonstrated that levels of 3-chlorotyrosine and 3-nitrotyrosine - two characteristic products of MPO - are elevated in HDL isolated from patients with established cardiovascular disease. When apolipoprotein A-I (apoA-I), the major HDL protein, is oxidized by MPO, its ability to promote cellular cholesterol efflux by the membrane-associated ATP-binding cassette transporter A1 (ABCA1) pathway is diminished. Biochemical studies revealed that oxidation of specific tyrosine and methionine residues in apoA-I contributes to this loss of ABCA1 activity. Another potential mechanism for generating dysfunctional HDL involves covalent modification of apoA-I by reactive carbonyls, which have been implicated in atherogenesis and diabetic vascular disease. Indeed, modification of apoA-I by malondialdehyde (MDA) or acrolein also markedly impaired the lipoprotein's ability to promote cellular cholesterol efflux by the ABCA1 pathway. Tandem mass spectrometric analyses revealed that these reactive carbonyls target specific Lys residues in the C-terminus of apoA-I. Importantly, immunochemical analyses showed that levels of MDA-protein adducts are elevated in HDL isolated from human atherosclerotic lesions. Also, apoA-I co-localized with acrolein adducts in such lesions. Thus, lipid peroxidation products might specifically modify HDL in vivo. Our observations support the hypotheses that MPO and reactive carbonyls might generate dysfunctional HDL in humans. This article is part of a Special Issue entitled Advances in High Density Lipoprotein Formation and Metabolism: A Tribute to John F. Oram (1945-2010).     

Diversity in the Integrase Coding Domain of a gypsy-like Retrotransposon Among Wild Relatives of Rice in the Oryza officinalis Complex

The Oryza officinalis complex is a genetically diverse, tertiary genepool of rice. We analyzed part of the primary structure of the integrase coding domain (ICD) of a gypsy-like retrotransposon from species of the O. officinalis species complex. PCR was performed with degenerate primers that hybridized to conserved sequences in the integrase genes of gypsy-type retrotransposons, using total DNA from different species of the O. officinalis complex as templates. Cloning and sequencing of the PCR products showed that the amplified fragments are highly homologous to each other (75–90%) and belong to one family of retrotransposons that is related to the previously studied RIRE-2 element from rice. Two main subfamilies of 292 and 351 bp were distinguished. Analysis of primary sequence data supports previous reports that sequence divergence during vertical transmission has been the major influence on the evolution of gypsy-type retrotransposons in Oryza species. Based on sequence data phylogenetic relationships among species of the O. officinalis complex were estimated. The data suggests that O. eichingeri is more closely related to the ancestral species of the complex. This revised version was published online in July 2006 with corrections to the Cover Date.     

pH-Dependent Conformational Changes in Bacterial Hsp90 Reveal a Grp94-Like Conformation at pH 6 That Is Highly Active in Suppression of Citrate Synthase Aggregation

The molecular chaperone Hsp90 depends upon large conformational rearrangements for its function. One driving force for these rearrangements is the intrinsic ATPase activity of Hsp90, as seen with other chaperones. However, unlike other chaperones, structural and kinetic studies have shown that the ATPase cycle of Hsp90 is not conformationally deterministic. That is, rather than dictating the conformational state, ATP binding and hydrolysis shift the equilibrium between a preexisting set of conformational states in an organism-dependent manner. While many conformations of Hsp90 have been described, little is known about how they relate to chaperone function. In this study, we show that the conformational equilibrium of the bacterial Hsp90, HtpG, can be shifted with pH. Using small-angle X-ray scattering, we identify a two-state pH-dependent conformational equilibrium for apo HtpG. Our structural modeling reveals that this equilibrium is observed between the previously observed extended state and a second state that is strikingly similar to the recently solved Grp94 crystal structure. In the presence of nonhydrolyzable 5′-adenylyl-β,γ-imidodiphosphate, a third state, which is identical with the solved AMPPNP-bound structure from yeast Hsp90, is populated. Electron microscopy confirmed the observed conformational equilibria. We also identify key histidine residues that control this pH-dependent equilibrium; using mutagenesis, we successfully modulate the conformational equilibrium at neutral pH. Using these mutations, we show that the Grp94-like state provides stronger aggregation protection compared to the extended apo conformation in the context of a citrate synthase aggregation assay. These studies provide a more detailed view of HtpG's conformational dynamics and provide the first linkage between a specific conformation and chaperone function.     

Functional characterization of a sucrose:fructan 6-fructosyltransferase of the cold-resistant grass Bromus pictus by heterelogous expression in Pichia pastoris and Nicotiana tabacum and its involvement in freezing tolerance

We have previously reported the molecular characterization of a putative sucrose:fructan 6-fructosyltransferase (6-SFT) of Bromus pictus, a graminean species from Patagonia, tolerant to cold and drought. Here, this enzyme was functionally characterized by heterologous expression in Pichia pastoris and Nicotiana tabacum. Recombinant P. pastoris Bp6-SFT showed comparable characteristics to barley 6-SFT and an evident fructosyltransferase activity synthesizing bifurcose from sucrose and 1-kestotriose. Transgenic tobacco plants expressing Bp6-SFT, showed fructosyltransferase activity and fructan accumulation in leaves. Bp6-SFT plants exposed to freezing conditions showed a significantly lower electrolyte leakage in leaves compared to control plants, indicating less membrane damage. Concomitantly these transgenic plants resumed growth more rapidly than control ones. These results indicate that Bp6-SFT transgenic tobacco plants that accumulate fructan showed enhanced freezing tolerance compared to control plants.     

Identifying Assembly-Inhibiting and Assembly-Tolerant Sites in the SbsB S-Layer Protein from Geobacillus stearothermophilus

Surface layer (S-layer) proteins self-assemble into two-dimensional crystalline lattices that cover the cell wall of all archaea and many bacteria. We have generated assembly-negative protein variants of high solubility that will facilitate high-resolution structure determination. Assembly-negative versions of the S-layer protein SbsB from Geobacillus stearothermophilus PV72/p2 were obtained using an insertion mutagenesis screen. The haemagglutinin epitope tag was inserted at 23 amino acid positions known to be located on the monomer protein surface from a previous cysteine accessibility screen. Limited proteolysis, circular dichroism, and fluorescence were used to probe whether the epitope insertion affected the secondary and tertiary structures of the monomer, while electron microscopy and size-exclusion chromatography were employed to examine proteins' ability to self-assemble. The screen not only identified assembly-compromised mutants with native fold but also yielded correctly folded, self-assembling mutants suitable for displaying epitopes for biomedical and biophysical applications, as well as cryo-electron microscopy imaging. Our study marks an important step in the analysis of the S-layer structure. In addition, the approach of concerted insertion and cysteine mutagenesis can likely be applied for other supramolecular assemblies.