Rotational and hinge dynamics of discoidal high density lipoproteins probed by interchain disulfide bond formation

To develop a detailed double belt model for discoidal HDL, we previously scored inter-helical salt bridges between all possible registries of two stacked antiparallel amphipathic helical rings of apolipoprotein (apo) A-I. The top score was the antiparallel apposition of helix 5 with 5 followed closely by appositions of helix 5 with 4 and helix 5 with 6. The rationale for the current study is that, for each of the optimal scores, a pair of identical residues can be identified in juxtaposition directly on the contact edge between the two antiparallel helical belts of apoA-I. Further, these residues are always in the '9th position' in one of the eighteen 11-mer repeats that make up the lipid-associating domain of apoA-I. To illustrate our terminology, 129j (LL5/5) refers to the juxtaposition of the Cα atoms of G129 (in a '9th position') in the pairwise helix 5 domains. We reasoned that if identical residues in the double belt juxtapositions were mutated to a cysteine and kept under reducing conditions during disc formation, we would have a precise method for determining registration in discoidal HDL by formation of a disulfide-linked apoA-I homodimer. Using this approach, we conclude that 129j (LL5/5) is the major rotamer orientation for double belt HDL and propose that the small ubiquitous gap between the pairwise helix 5 portions of the double belt in larger HDL discoidal particles is significantly dynamic to hinge off the disc edge under certain conditions, e.g., in smaller particles or perhaps following binding of the enzyme LCAT. 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).     

中国生物医药R&D的发展研究

就当前制约我国生物医药发展的影响因素进行了全面、细致地分析,并相应地对下一步生物医药R＆D的发展提出设想.     

The genome of Syntrophorhabdus aromaticivorans strain UI provides new insights for syntrophic aromatic compound metabolism and electron flow

How aromatic compounds are degraded in various anaerobic ecosystems (e.g. groundwater, sediments, soils and wastewater) is currently poorly understood. Under methanogenic conditions (i.e. groundwater and wastewater treatment), syntrophic metabolizers are known to play an important role. This study explored the draft genome of Syntrophorhabdus aromaticivorans strain UI and identified the first syntrophic phenol‐degrading phenylphosphate synthase (PpsAB) and phenylphosphate carboxylase (PpcABCD) and syntrophic terephthalate‐degrading decarboxylase complexes. The strain UI genome also encodes benzoate degradation through hydration of the dienoyl‐coenzyme A intermediate as observed in Geobacter metallireducens and Syntrophus aciditrophicus. Strain UI possesses electron transfer flavoproteins, hydrogenases and formate dehydrogenases essential for syntrophic metabolism. However, the biochemical mechanisms for electron transport between these H₂/formate‐generating proteins and syntrophic substrate degradation remain unknown for many syntrophic metabolizers, including strain UI. Analysis of the strain UI genome revealed that heterodisulfide reductases (HdrABC), which are poorly understood electron transfer genes, may contribute to syntrophic H₂ and formate generation. The genome analysis further identified a putative ion‐translocating ferredoxin : NADH oxidoreductase (IfoAB) that may interact with HdrABC and dissimilatory sulfite reductase gamma subunit (DsrC) to perform novel electron transfer mechanisms associated with syntrophic metabolism.     

The polyadenylated RNA directing the synthesis of the rat myelin basic proteins is present in both free and membrane-bound forebrain polyribosomes.

Free and membrane-bound polyribosomes were isolated from the forebrain of actively myelinating 24-day-old rats. The poly(A)+ RNA (polyadenylated RNA) extracted from both fractions was translated in vitro in reticulocyte lysates [Hall & Lim (1981) Biochem. J. 196. 327-336] in the presence or absence of a heterologous microsomal membrane fraction from dog pancreas. The rat myelin basic proteins synthesized in vitro were isolated by CM-cellulose chromatography and by immunoprecipitation with purified anti-(myelin basic protein) antibody. The large (mol.wt. 18 500) and small (mol.wt. 16 000) myelin basic proteins were translational products of poly(A)+ RNA from both free and membrane-bound polyribosomes. The identity of the myelin basic proteins was verified by analysis of peptides generated by the cathepsin D digestion of the immunoprecipitated proteins synthesized in vitro, in comparison with authentic rat myelin basic proteins. Although several other translational products of membrane-bound polyribosomal poly(A)+ RNA were modified when microsomal membranes were present during translation, molecular weights of the myelin basic proteins themselves were unchanged. The myelin basic proteins synthesized in vitro also did not differ significantly in size from the authentic myelin basic proteins, indicating that these membrane proteins are unlikely to be synthesized as substantially larger precursor molecules. The presence of the specific mRNA species on both free and membrane-bound polyribosomes is compatible with the extrinsic location of the myelin basic proteins on the cytoplasmic surface of the myelin membrane.     

Sequence analysis and structural prediction of the severe acute respiratory syndrome coronavirus nsp5

The non-structural proteins (nsp or replicase proteins) of coronaviruses are relatively conserved and can be effective targets for drugs. Few studies have been conducted into the function of the severe acute respiratory syndrome coronavirus (SARS-CoV) nsp5. In this study, bioinformatics methods were employed to predict the secondary structure and construct 3-D models of the SARS-CoV GD strain nsp5. Sequencing and sequential comparison was performed to analyze the mutation trend of the polymerase nsp5 gene during the epidemic process using a nucleotide-nucleotide basic local alignment search tool (BLASTN) and a protein-protein basic local alignment search tool (BLASTP). The results indicated that the nsp5 gene was steady during the epidemic process and the protein was homologous with other coronavirus nsp5 proteins. The protein encoded by the nsp5 gene was expressed in COS-7 cells and analyzed by sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE). This study provided the foundation for further exploration of the protein‘s biological function, and contributed to the search for anti-SARS-CoV drugs.     

宁夏河东沙区刺槐和丝绵木水分利用策略

刺槐和丝绵木混交林是宁夏河东沙区防护林建设的主要模式,了解刺槐和丝绵木的水分利用策略,能为区域植被恢复和防护林林分结构调整提供科学依据。以宁夏河东沙区刺槐(Robinia pseudoacacia)和丝绵木(Euonymus bungeanus)混交林为研究对象,通过监测微气象、树干液流和土壤质量含水量,结合大气降水、土壤水、植物木质部水同位素组成,采用Granier及其校正公式,运用贝叶斯混合模型(MixSIAR)和相似性比例指数(PS)研究2个树种的蒸腾耗水、水分来源和水分利用关系。结果表明：刺槐和丝绵木的蒸腾耗水量在生长季中期较高,前期和后期较小,刺槐的蒸腾耗水量是丝绵木的1.55倍;影响刺槐蒸腾耗水的主要环境因子为饱和水汽压差、太阳辐射、0—40 cm土壤质量含水量和40—120 cm土壤质量含水量;影响丝绵木蒸腾耗水的主要环境因子为饱和水汽压差、太阳辐射、平均气温、0—40 cm土壤质量含水量和40—120 cm土壤质量含水量;蒸腾耗水较高时,刺槐主要吸收利用中层土壤水,丝绵木主要吸收利用浅层土壤水,蒸腾耗水较低时,刺槐主要吸收利用浅层土壤水,丝绵木主要吸收利用中层土壤水;在...     

土壤含水量对桔小实蝇蛹期存活的影响

浸水时间、土壤含水量对桔小实蝇Bactroceradorsalis(Hendel)蛹的存活及成虫羽化的影响的研究结果表明:(1)不同浸水时间对桔小实蝇蛹存活率的影响不同。浸水时间越长,蛹存活率越低;浸水对初期蛹的影响较大,蛹龄越大,浸水作用效果越低。浸水时间(TW)、蛹期(AP)和蛹存活率(SP)之间关系符合以下模型:SP=0.4165-0.00307TW+0.2290AP-0.00004496T2W-0.0002528A2P+0.00008258TWAP。(2)土壤含水量对桔小实蝇成虫羽化影响明显。当土壤含水量较低或较高时,羽化率都明显受到抑制。相对含水量在30%～80%之间,蛹的羽化率较高。相对含水量(Ws)和成虫羽化率(E)之间存在以下关系:E=0.396+0.01985W-0.000181W2。     

1980s-2010s华北夏谷区主栽谷子品种SSR遗传多样性分析

通过对20世纪80年代以来具有代表性的华北夏谷区审(鉴)定的20个主栽谷子品种进行SSR标记多态性分析,研究了华北地区育成谷子品种的遗传多样性。49对引物在20个谷子品种中扩增出具有多态性的条带,共检测出142个等位变异,平均每个位点检测出的等位变异数为2.96个。标记位点多态性信息含量(PIC)变幅为0.0904～0.6896,平均为0.4168。20份材料间的遗传距离变幅为0.0173～0.9000,聚类分析将其分成3个类群,其中谷丰1号自成一类,表明谷丰1号的遗传距离较其他品种大。不同年代谷子品种间遗传距离分析结果显示,各年代品种之间的平均遗传距离由大到小依次是1980s>1990s>2000s>2010s,表明随着年代的递进育成品种的遗传差异减小,亲缘关系增近。