高粱泡果实营养评价及其种子油脂肪酸组分的分析

分析测定了福建产的高粱泡果实营养成分及其种子油脂肪酸组分。结果表明：其果实含总酸量高,达3.37%,蛋白质含量为6.81%,氨基酸为6.33g/100g.DW,必需氨基酸占氨基酸总量的25.81%;SOD含量高达275.03u/g.FW;矿质元素含量丰富,尤其是Fe、Zn等;种子油以不饱和脂肪酸为主,其中亚油酸（51.7%-52.2%）、α－亚麻酸(33.1%-34.8%)和油酸(6.4%-8.5%)较丰富。此外,含丰富粗脂肪、糖类、维生素等营养物质,高粱泡资源丰富、营养价值和医疗保健作用高,具有较大的开发利用潜力。     

The SER primer and climate change

The SER Primer on Ecological Restoration provides a succinct introduction to, and overview of, the rapidly growing field of ecological restoration. The Primer was issued initially in 2002 by the Society for Ecological Restoration (SER) and reissued verbatim 2 years later in a more attractive format ( http://www.ser.org/resources;resources-detail-view/ser-international-primer-on-ecological-restoration ). A SER committee recently began deliberations to update the Primer, and much discussion is underway. As two of the Primer's principal authors, we were invited to share our views on how the Primer can be advantageously revised in the light of any changes or new insights since 2002. In particular, we were asked how the Primer might be modified to reflect the ways that ecological restoration address conservation issues raised by climate change and other rapid environmental shifts and global changes. We also touch on questions relating to the benefits of ecological restoration to human society, as this is an area where the Primer needs sharper focus. We have structured the following in a ‘Frequently Asked Questions’ format to highlight issues raised in the recent literature and to focus attention on other issues that merit consideration in the Primer revision process.     

菌紫质的Ser和Lys残基修饰对BR结构和功能的影响

用化学修饰研究了菌紫质（ＢＲ）的结构和功能的变化。用氮氧自由基分别对赖氨酸和丝氨酸进行修饰,研究结果表明在圆二色谱上（ＣＤ谱）,与天然紫膜样品比较,两种自由基分别修饰赖氨酸（Ｌｙｓ）和丝氨酸（Ｓｅｒ）残基２４小时后的ＣＤ谱中均只有负峰,分别在５９６ｎｍ和６０２ｎｍ,５３５ｎｍ的正峰已消失,７２小时后５３５ｎｍ的正峰部分地恢复,但１２０小时后均未见进一步恢复。与未修饰的紫膜相比,两种自由基修饰的紫膜在Ｒａｍａｎ光谱上观察到中间体Ｍ４１２的相对量要明显增加。本文对这二种化学修饰引起的ＢＲ结构和功能变化进行了初步讨论。     

金花茶胚状体中游离氨基酸的含量及花氨酸、丝氨酸对胚状体发育的影响

本文报道金花茶Camellia chrysantha(HU)Tuyama胚状体培养中,具有正常产生次级胚能力的材料(第一类)和产生次胚能力差的材料(第二类)的游离氨基酸测定结果,以及脯氨酸、丝氨酸对胚状体发生的培养结果。所检出的氨基酸含量,第一类材料为第二类材料的1—5倍;且第二类材料中未能检出脯氨酸,苯丙氨和酪氨酸。在此基础上培养发现:脯氨酸和低浓度(50mmol、100mmol)的丝氨酸促进胚状体发生与鲜重增加,脯氨酸、丝氨酸和苯丙氨酸以50mmol混合使用效果最好,而且除色氨酸外,这些外加氨基酸对胚体形成频率、数目和鲜重的影响之间都有平行关系。     

Endothelial NO synthase phosphorylated at SER635 produces NO without requiring intracellular calcium increase

Shear stress stimulates NO production involving the Ca2+-independent mechanisms in endothelial cells. We have shown that exposure of bovine aortic endothelial cells (BAEC) to shear stress stimulates phosphorylation of eNOS at S635 and S1179 by the protein kinase A- (PKA-) dependent mechanisms. We examined whether phosphorylation of S635 of eNOS induced by PKA stimulates NO production in a calcium-independent manner. Expression of a constitutively active catalytic subunit of PKA (Cqr) in BAEC induced phosphorylation of S635 and S1179 residues and dephosphorylation of T497. Additionally, Cqr expression stimulated NO production, which could not be prevented by treating cells with the intracellular calcium chelator BAPTA-AM. To determine the role of each eNOS phosphorylation site in NO production, HEK-293 cells transfected with eNOS point mutants whereby S116, T497, S635, and S1179 were mutated to either A or D. Maximum NO production from S635D-expressing cells was significantly higher than that of either wild type or S635A in both basal and elevated [Ca2+]i conditions. More interestingly, S635D cells produced NO even when [Ca2+]i was nearly depleted by BAPTA-AM. We confirmed these results obtained in HEK-293 cells in BAEC transfected with S635D, S635A, or wild-type eNOS vector. These findings suggest that, once phosphorylated at S635 residue, eNOS produces NO without requiring any changes in [Ca2+]i. PKA-dependent phosphorylation of eNOS S635 and subsequent basal NO production in a Ca2+-independent manner may play an important role in regulating vascular biology and pathophysiology.     

ALLOZYME VARIATION WITHIN SOLANUM SECT. PETOTA,SER. ETUBEROSA (SOLANACEAE)

Enzyme electrophoresis was employed to measure genetic variation within and divergence among 32 populations of three species in Solanum sect. Petota (S. brevidens, S. etuberosum, and S. fernandezianum). These species are self-compatible, diploid (2n = 2x = 24), and members of the monophyletic series Etuberosa. Solanum etuberosum is distributed in southern Chile, S. brevidens occurs in southern Chile and adjacent southern Argentina, and S. fernandezianum is endemic to Masatierra Island in the Juan Fernández Archipelago, 650 km west of continental Chile. Very low levels of observed heterozygosity (0.00–0.04) are found within populations of all three species. Interspecific mean genetic identities between S. brevidens and S. etuberosum (0.854) were similar to their intraspecific values (0.923, 0.865, respectively), with both species monomorphic for alleles at nine of the 12 loci examined. Solanum fernandezianum shows no heterozygosity and is more divergent to both S. brevidens (0.780) and S. etuberosum (0.698) than either is to each other. The divergence of S. fernandezianum to S. brevidens and S. etuberosum results from novel alleles at two of the 12 isozyme loci; in addition, it possesses only a subset of the variability found in S. brevidens and S. etuberosum at three other loci.     

Activation of fusion by the SER virus F protein: a low-pH-dependent paramyxovirus entry process

SER virus, a paramyxovirus closely related to simian virus 5, induces no syncytium formation. The SER virus F protein has a long cytoplasmic tail (CT), and truncation or mutations of the CT result in enhanced syncytium formation (S. Seth, A. Vincent, and R. W. Compans, J. Virol. 77:167-178, 2003; S. Tong, M. Li, A. Vincent, R. W. Compans, E. Fritsch, R. Beier, C. Klenk, M. Ohuchi, and H.-D. Klenk, Virology 301:322-333, 2002). We hypothesized that the presence of the long CT serves to stabilize the metastable conformation of the F protein. We observed that the hemifusion, cytoplasmic content mixing, and syncytium formation ability of the wild-type SER virus F coexpressed with the SER virus hemagglutinin-neuraminidase (HN) protein was enhanced, both qualitatively and quantitatively, at elevated temperatures. We also observed enhanced hemifusion, content mixing, and syncytium formation in SER virus F- and HN-expressing cells at reduced pH conditions ranging between 4.8 and 6.2. We have obtained evidence that in contrast to other paramyxoviruses, entry of SER virus into cells occurs by a low-pH-dependent process, indicating that the conversion to the fusion-active state for SER virus F is triggered by exposure to reduced pH.     

Glycosylation and Sialylation of Macrophage-derived Human Apolipoprotein E Analyzed by SDS-PAGE and Mass Spectrometry: EVIDENCE FOR A NOVEL SITE OF GLYCOSYLATION ON SER290*

Apolipoprotein E (apoE) is a 34-kDa glycoprotein secreted from various cells including hepatocytes and macrophages and plays an important role in remnant lipoprotein clearance, immune responses, Alzheimer disease, and atherosclerosis. Cellular apoE and plasma apoE exist as multiple glycosylated and sialylated glycoforms with plasma apoE being less glycosylated/sialylated than cell-derived apoE. Some of the glycan structures on plasma apoE are characterized; however, the more complicated structures on plasma and cellular/secreted apoE remain unidentified. We investigated glycosylation and sialylation of cellular and secreted apoE from primary human macrophages by one- and two-dimensional gel electrophoresis and mass spectrometry. Our results identify eight different glycoforms with (HexNAc)₂-Hex₂-(NeuAc)₂ being the most complex glycan detected on Thr¹⁹⁴ in both cellular and secreted apoE. Four additional glycans were identified on apoE(283–299), and using β-elimination/alkylation by methylamine in vitro, we identified Ser²⁹⁰ as a novel site of glycan attachment. Comparison of plasma and cellular/secreted apoE from the same donor confirmed that cell-derived apoE is more extensively sialylated than plasma apoE. Given the importance of the C terminus of apoE in regulating apoE solubility, stability, and lipid binding, these results may have important implications for our understanding of apoE biochemistry.Apolipoprotein E (apoE)¹ is a 34-kDa glycosylated apolipoprotein of 299 amino acids. ApoE is synthesized and secreted by most cells including hepatocytes, smooth muscle cells, neuronal cells, and macrophages (1–3) and demonstrates extraordinary functional diversity. It has important roles in remnant lipoprotein clearance, the immune response, Alzheimer disease, cell proliferation, and lymphocyte activation (4, 5). More recent studies suggest that elevated plasma apoE precedes elevation of C-reactive protein and confers increased risk of cardiovascular death in the elderly (6). Proteomics-based approaches have identified elevated high density lipoprotein (HDL)-apoE as being associated with coronary disease (7). In contrast, macrophage-specific expression of apoE protects against atherosclerosis in mice (8, 9). The mechanisms by which macrophage apoE is antiatherogenic may include stimulating the removal of excess cholesterol from macrophage foam cells as well as anti-inflammatory, antiproliferative, and immunomodulatory properties (4, 5, 10–12). An accurate understanding of the structure of apoE secreted from macrophages is important for our understanding of its properties and its role in the atherosclerotic process.Structural studies on apoE have provided important insights into its biological properties (13). Crystallography has demonstrated that the N-terminal domain is structured in a globular four-helix bundle with the helices orientated in an antiparallel alignment (14). The structure of the C terminus has not been resolved by crystallography, but circular dichroism spectroscopy indicates it to be highly α-helical (14). Recently, NMR studies of monomeric, full-length human apoE indicated that the C-terminal domain in the intact protein adopts a more defined structure than it does as an isolated fragment (15). Lipid binding occurs at the C terminus (residues 244–272), resulting in unfolding of the molecule into a helical hairpin with the binding region for the low density lipoprotein (LDL) receptor contained within the N terminus at its apex (16).Mucin-type O-glycosylation is a particularly common, complex, and important post-translational modification of secreted and cell surface glycoproteins (17, 18) that is difficult to accurately characterize; however, several recent reports have facilitated analysis (19, 20). Cellular apoE and plasma apoE exist as multiple glycoforms, which vary in charge because of variable sialylation. The initial analysis of the carbohydrate content of plasma very low density lipoprotein (VLDL)-apoE by colorimetric methods and gas chromatography demonstrated that the major unmodified hexose in apoE was galactose and that N-acetylglucosamine, N-acetylgalactosamine, and sialic acid were present (21, 22). Two-dimensional gel electrophoresis (2-DE) identified up to six sialylated apoE (Es) glycoforms in cells for any given genotype and fewer sialylated glycoforms in plasma (22). ApoE does not contain the consensus sequence (NX(T/S/C)) required for N-linked glycans, and carbohydrate residues are attached to apoE via an O-linkage to residue Thr¹⁹⁴ (23–25). More recent studies using 2-DE and MALDI-TOF/TOF (23) confirmed previous results and identified five glycosylated glycoforms of apoE in plasma VLDL with the most complex sugar structures containing two sialic acid residues (HexNAc-Hex-NeuAc-NeuAc). There were more negatively charged glycoforms present on 2-DE than were distinguished by MALDI-TOF/TOF, raising the possibility that complex structures containing more than two sialic acid residues may be inherently unstable during MS analysis. Importantly, this recent study did not analyze apoE glycoforms in, or secreted from, cells.The purpose of this study was to undertake the first detailed characterization of the glycan structures of apoE from primary human macrophages by 1-DE, 2-DE, and mass spectrometry. We found that cellular and secreted apoE in human macrophages has at least eight different glycoforms with (HexNAc)₂-Hex₂-(NeuAc)₂ being the most complex glycan identified. We extend previous studies by the identification of a novel site of glycan attachment on Ser²⁹⁰ near the functionally important apoE C terminus in addition to glycosylation of Thr¹⁹⁴ and show that a major glycoform is present in each of the spots separated by 2-DE.     

Synthesis of L-Sangivamycin and Toyocamycin Analogues and Their Inhibitory Activities of SER/THR Protein Kinases

Abstract

Novel _l-sangivamycin and toyocamycin analogues were synthesized and evaluated for Cdc2 protein kinase activity. Among the compounds tested, _l-xylose derivative and _l-arabinose derivative exhibited potent inhibitory activity against Cdc2 protein kinase with IC₅₀ values of 3.7 and 1.6 μM, respectively.     

Molecular docking analysis of bioactive compounds from Mollugo cerviana (L.) SER with DHFR for antifungal activity

Fungal infections have been increasing in recent years due to growing number of high-risk patients particularly immuno compromised hosts. Candida is the third- or fourth-most-common isolate in nosocomial bloodstream infections. The increase of fungal resistance to classical drugs, the treatment costs, and the fact that most available antifungal drugs have only fungistatic activity, justify the search for new strategies. Identification of therapeutic compounds from plants has been the centre of attraction ever since they were discovered. It is of interest to document the molecular docking analysis of bioactive compounds present in Mollugo cerviana (L.) SER with the DHFR protein target for antifungal activity. We show the optimal binding features of several compounds from the extract with in vivo and in vitro activities. Results of this showed that all compounds showed good antimicrobial activity and a very good antifungal activity against the target DHFR protein. So, these compounds may act as potential drug molecules after the experimental validation.     

Matrix metalloproteinase-7 activation of mouse paneth cell pro-alpha-defensins: SER43 down arrow ILE44 proteolysis enables membrane-disruptive activity

Small intestinal Paneth cells secrete alpha-defensin microbicidal peptides as mediators of innate enteric immunity. In mice, production of mature Paneth cell alpha-defensins, termed cryptdins (Crps), requires proteolytic activation of inactive precursors (pro-Crps) by the convertase matrix metalloproteinase-7. Proteolysis of mouse (pro-Crp4)(20-92) produces the specific cleavage intermediates pro-Crp4(44-92), pro-Crp4(54-92), and pro-Crp4(59-92). To identify which cleavage event enables bactericidal activity, recombinant pro-Crp4-processing intermediates were purified to homogeneity and assayed for bactericidal peptide activity. The in vitro bactericidal activities of pro-Crp4-processing intermediates were very similar to fully processed Crp4, contrasting the lack of bactericidal and membrane-disruptive activity shown by pro-Crp4(20-92). Thus, cleavage of pro-Crp4(20-92) at Ser(43) downward arrowIle(44) is sufficient to activate bactericidal activity, and amino acids in the pro-Crp4(20-43) of the proregion maintain the precursor in an inactive state. Because cationic Arg residues are determinants of Crp4 bactericidal peptide activity, we hypothesized that Asp and Glu residues in pro-Crp4(20-43) neutralize Crp4 Arg side chains in pro-Crp4(20-92). Therefore, a pro-Crp4(20-92) variant with Gly substitutions at all pro-Crp4(20-43) Asp and Glu positions ((DE/G)-pro-Crp4) was prepared, and it was bactericidal and lysed phospholipid vesicles under conditions where native pro-Crp4(20-92) lacks activity. These findings show that MMP-7 proteolysis of pro-Crp4(20-92) at Ser(43) downward arrowIle(44) converts inactive precursors to bactericidal forms by removal of covalently associated, inhibitory acidic amino acids from proximity with the Crp4 component of the molecule.     

中国蹄盖蕨属轴果蹄盖蕨系的研究

本文是中国蹄盖蕨属植物研究的系列论文的第三篇,对国产轴果蹄盖蕨系植物进行了分类学订正,详细记载了中国产该系植物11种,首次将20余个名称归入该系的一些种下做为异名处理。轴果蹄盖蕨系植物是蹄盖蕨属中自然的一群,以其铁角蕨类型的孢子囊群和囊群益与其它属下类群相区别。本系植物分布于亚洲热带和亚热带山地,常见于山地常绿阔叶林下,海拔500～1800m。在华中和华东地区其分布区北界不超过长江一线。中国西南地区和台湾及日本为该系的三个分化中心。