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PbPH5,an H^(+)P-ATPase on the tonoplast,is related to malic acid accumulation in pear fruit 被引量:2
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作者 SONG Jun-xing CHEN Ying-can +6 位作者 LU Zhao-hui ZHAO Guang-ping WANG Xiao-li ZHAI Rui WANG Zhi-gang YANG Cheng-quan XU Ling-fei 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2022年第6期1645-1657,共13页
Organic acid content is one of the most important factors influencing fruit flavors.The predominant organic acid in most pear cultivars is malic acid,but the mechanism controlling its accumulation remains unclear.In t... Organic acid content is one of the most important factors influencing fruit flavors.The predominant organic acid in most pear cultivars is malic acid,but the mechanism controlling its accumulation remains unclear.In this study,by comparing gene expression levels and organic acid contents,we found that the expression of PbPH5,which encodes a P_(3A)-ATPase,is highly correlated with malic acid accumulation in four different pear species,with correlation coefficients of 0.932**,0.656*,0.900**,and 0.518*(*,P<0.05;**,P<0.01)for Pyrus bretschneideri Rehd.,P.communis Linn.,P.pyrifolia Nakai.,and P.ussuriensis Maxim.,respectively.Moreover,the overexpression of PbPH5 in pear significantly increased the malic acid content.In contrast,silencing PbPH5 via RNA interference significantly decreased both its transcript level and the pear fruit malic acid content.A subcellular localization analysis indicated that PbPH5 is located in the tonoplast.Additionally,a phylogenetic analysis indicated that PbPH5 is a PH5 homolog gene that is clustered with the Petunia hybrida,Malus domestica,and Citrus reticulata genes.Considered together,these findings suggest that PbPH5 is a functionally conserved gene.Furthermore,the accumulation of malic acid in pear fruit is at least partly related to changes in the PbPH5 transcription levels. 展开更多
关键词 PEAR P3A-ATPase PH5 homolog malic acid accumulation proton pump
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Trace determination of cobalt ion by using malic acid-malonic acid double substrate oscillating chemical system 被引量:1
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作者 Jie Wang Wu Yang Jie Ren Miao Guo Xiao Dong Chen Wen Bin Wang Jin Zhang Gao 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第9期1103-1107,共5页
A novel kinetic method for determination of trace amounts of cobalt ion was proposed and validated. The method is based on adding malic acid into classical Belousov-Zhabotinskii (B-Z) oscillating chemical system to ... A novel kinetic method for determination of trace amounts of cobalt ion was proposed and validated. The method is based on adding malic acid into classical Belousov-Zhabotinskii (B-Z) oscillating chemical system to form a double substrate one. The results showed that when the concentration of cobalt ion was in the range of 5.27× 10^-8 to 5.37 × 10^-12 mol L^-1, the change of the oscillating period was directly proportional to the negative logarithm of cobalt ion concentration. The sensitivity and precision of the developed method were quite satisfactory. The limit of detection was down to 5.20 × 10^-13 mol L^-1 which was a highest sensitivity found for determination of metal ions using oscillating chemical reaction so far. Some factors influencing the determination were also examined. The method has been successfully used to determine cobalt ion in vitamin B12 injection. 展开更多
关键词 Two substrate oscillating chemical system malic acid COBALT Determination
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A convenient synthesis of methyl 2-hydroxy-4-oxo-4-(substituted phenyl) butanoates from malic acid
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作者 Yong Zhang M. NaseerA. Khan +1 位作者 Ping Gong Yong Sup Lee 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第8期898-900,共3页
A synthesis of methyl 2-hydroxy-4-oxo-4-(substituted phenyl)butanoates has been accomplished using Friedel-Crafts acylation of substituted benzenes with 2-acetoxybutanoyl chloride. The key feature of this strategy i... A synthesis of methyl 2-hydroxy-4-oxo-4-(substituted phenyl)butanoates has been accomplished using Friedel-Crafts acylation of substituted benzenes with 2-acetoxybutanoyl chloride. The key feature of this strategy is that various 4-arylbutanoates can be obtained conveniently, which are important intermediates for the synthesis of biologically active compounds including ACE inhibitors.?2009 Yong Sup Lee. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved. 展开更多
关键词 2-Hydroxy-4-oxo-4-phcnylbutanoatcs malic acid Fricdel-Crafts reaction
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Complexation of Molybdenum (Ⅵ) with R-and S-malic Acid, The Crystal Structure of (NH_4)_4[(MoO_2)_4O_3(R-mal)_2]·6H_2O
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作者 周朝晖 杨文斌 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 1995年第4期255-260,共6页
Ammonium tetramolybdate ( NH4 )4[(MoO2)4O3 (R-mal)2]·6H2O(mal= malic acid)and (NH4)4[(MoO2)4O3(S-mal)2)·6H2O have been prepared by the reaction of R and S-malic acid with ammonium heptamolybdate, respectivel... Ammonium tetramolybdate ( NH4 )4[(MoO2)4O3 (R-mal)2]·6H2O(mal= malic acid)and (NH4)4[(MoO2)4O3(S-mal)2)·6H2O have been prepared by the reaction of R and S-malic acid with ammonium heptamolybdate, respectively. The two complexes are enantiomeric and isomorphous. The complex of Risomer crystallizes in monoclinic space group C2 with unit cell parameters:a = 14. 591 (2 ), b = 10. 108(2), c=11. 464(2), β=121. 48(1)°, V=1441. 9(4),Z=2, Fω=1002. 13, Dc=2. 308, Dm=2. 3 g/cm3. F(000) = 988, MoKα radiation (λ=0. 71073 ), μ (MoKα) = 17. 7 cm-1. Final R=0. 027 for 1491 reflections with I>2. 5 σ(I). Analysis of molecular structure reveals that the complex anion contains a (Mo2O5)O(Mo2O5)core with the bridging oxo-group passing through two-fold axis. Each molybdenum is hexacoordinated , and the malate ligand is quadridentated to two molybdenum atoms by the deprotonated hydroxy-, α- and β-carboxylate groups. Principal dimensions are:[Mo=O(t)]av, 1. 705(6); [Mo-O(b)]av, 1. 920(6); Mo-O(hydroxy). 1. 925(6);Mo-O(α-carboxy), 2. 226 (6), and [Mo-O(β-carboxy)av, 2. 296 (5).Lattice water is distributed throughout the cell and together with various types of the anion oxygens, making H-bonding. 展开更多
关键词 malic acid molate-molybdate complex crystal structure
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Preliminary Study on Lipase-catalyzed Synthesis of Polyesters Containing L-Malic Acid Units
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作者 Da Hu YAO Guang Ji LI 《Chinese Chemical Letters》 SCIE CAS CSCD 2006年第12期1611-1614,共4页
Terpolymer of 1, 8-octanediol, adipic acid, and L-malic acid was synthesized via a lipase-catalyzed direct polycondensation. The products were characterized by GPC and 1H NMR. The results indicated that the molecular ... Terpolymer of 1, 8-octanediol, adipic acid, and L-malic acid was synthesized via a lipase-catalyzed direct polycondensation. The products were characterized by GPC and 1H NMR. The results indicated that the molecular weight of the prepared polymers decreased with increasing L-malic acid content in the monomer feed ratio, and that change in the L-malic acid content from 0 to 20 mol % did not remarkably influenced on the molecular weight distribution Mw /Ma of the prepared samples. The 1H NMR spectra of the obtained copolymer samples showed that hydroxyl groups of L-malic acid did not take part in the polymerization reaction. 展开更多
关键词 L-malic acid POLYCONDENSATION LIPASE polyester.
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PREPARATION AND CELL COMPATIBILITY OF FUNCTIONALIZED BIODEGRADABLE POLY(DL-LACTIDE-co-RS-β-MALIC ACID)
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作者 何斌 顾忠伟 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 2008年第2期177-186,共10页
In order to create a functionalized biodegradable polymer for vascular tissue engineering application,poly(DL- lactide-co-RS-β-malic acid)(PDLLMAc)was synthesized.PDLLMAc was obtained after hydrogenolysis of poly(DL-... In order to create a functionalized biodegradable polymer for vascular tissue engineering application,poly(DL- lactide-co-RS-β-malic acid)(PDLLMAc)was synthesized.PDLLMAc was obtained after hydrogenolysis of poly(DL- lactide-co-RS-β-benzyl malolactonate)(PDLLMA),which was from the ring-opening polymerization of DL-lactide(DLLA) and RS-β-benzyl malolactonate(MA)using stannous octoate as catalyst.The copolymers were characterized by ~1H-NMR, FTIR,GPC and DSC.The tensile strength and water uptake of the copoly... 展开更多
关键词 BIODEGRADABLE Functionalization Poly(DL-lactide-co-RS-β-malic acid Tissue engineering.
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Effect of Phenolic Compounds on the Growth and L-Malic Acid Metabolism of Oenococcus oeni
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作者 Silvia Jane Lombardi Patrizio Tremonte +6 位作者 Mariantonietta Succi Bruno Testa Gianfranco Pannella Luca Tipaldi Elena Sorrentino Raffaele Coppola Massimo Iorizzo 《Journal of Life Sciences》 2012年第11期1225-1231,共7页
The effect of some phenolic compounds recurrent in wines on technological features of Oenococcus oeni was studied in order to individuate those strains to be utilized as starter in the deacidification of aged red wine... The effect of some phenolic compounds recurrent in wines on technological features of Oenococcus oeni was studied in order to individuate those strains to be utilized as starter in the deacidification of aged red wines. For this purpose, the growth and the L-malic acid metabolism of 100O. oeni strains, previously isolated from different wines, was assayed in a synthetic medium added with ethanol, malic acid and phenol carboxylic (gallic, caffeic, p-coumaric and ferulic) acids or flavonoids (catechin and quercetin) at different concentrations. Results evidenced a different sensitivity of strains to each assayed compound. All the compounds restrained or stimulated the growth of 57 and 11 strains respectively, while no effect was detected on 6 strains. The remaining 26 strains showed a different behaviour: all were restrained by ferulic acid and stimulated by gallic acid and catechin. As for caffeic acid, 17 out of 26 strains were restrained, while 9 strains were stimulated. The main result obtained in this study was the establishment of a relationship between the effect of phenolic compounds on the O. oeni growth and the behaviour of the malolactic fermentation. This study may enrich the selection criteria of strains for the deacidification of aged red wines. 展开更多
关键词 Phenol carboxylic acids FLAVONOIDS lactic acid bacteria malic acid metabolism.
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Highly selective/enantioselective Pt-ReOx/C catalyst for hydrogenation of L-malic acid at mild conditions
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作者 Bair S.Bal'zhinimaev Eugene A.Paukshtis +1 位作者 Alexey P.Suknev Nikita V.Makolkin 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2018年第3期903-912,共10页
The catalyst preparation strategy was based on a strict introduction sequence of rhenium and platinum precursors and their strong interaction with carbon support resulted in the formation of 0.5 nm Pt-Re Ox species of... The catalyst preparation strategy was based on a strict introduction sequence of rhenium and platinum precursors and their strong interaction with carbon support resulted in the formation of 0.5 nm Pt-Re Ox species of atomic dispersion, where platinum is metallic, while monolayer rhenium is partially oxidized(Re2+). The reaction kinetics was studied taking into account the process of L-malic acid association leading to the formation of inactive cyclic oligomeric species. High TOFs(ca. 50 h-1), selectivities(ca. 99%)and stability of Pt-Re Ox/C catalysts in aqueous-phase hydrogenation of L-malic acid, which are close to those of the homogeneous pincer type complexes, were revealed at mild conditions(T = 90–130 ℃). Taking into account that(i) hydrogenation reaction occurred 2–3 orders of magnitude faster than its racemization and(ii) association of L-malic acid dominates at low temperatures and in a concentrated solution,special reaction conditions that allow obtaining chemically and optically(ee 〉 99%) pure(S)-3-hydroxy-γ-butyrolactone and(S)-1,2,4-butanetriol were found. Basing on HAADF-STEM, EDX, XPS, and kinetic studies, the structure of active species and basic reaction pathways are proposed. 展开更多
关键词 L-malic acid Hydrogenation Enantioselectivity Platinum Rhenium Atomic dispersion
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Malic enzyme 3 mediated the effects of malic acid on intestinal redox status and feed efficiency in broilers
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作者 Hongfeng Jiang Genghui Li +6 位作者 Xue Yang Xiaohua Feng Penglin Li Huisi Yang Demin Cai Qingyan Jiang Gang Shu 《Journal of Animal Science and Biotechnology》 2025年第2期913-930,共18页
Background Intestinal oxidative stress serves as an endogenous host defense against the gut microbiota by increas-ing energy expenditure and therefore decreasing feed efficiency(FE).Several systems coordinately regula... Background Intestinal oxidative stress serves as an endogenous host defense against the gut microbiota by increas-ing energy expenditure and therefore decreasing feed efficiency(FE).Several systems coordinately regulate redox bal-ance,including the mitochondrial respiratory chain,nicotinamide adenine dinucleotide phosphate(NADPH)oxidase,and different antioxidants.However,it remains unclear which redox balance compartments in the intestine are crucial for determining FE.Results In this study,we first screened the key targets of different metabolites and redox balance-related gene expression in broiler ceca.We then constructed a mouse colitis model to explore malic acid(MA)ability to allevi-ate intestinal inflammation.We further used controlled release technology to coat MA and investigated its effects on the intestinal redox status and FE in vivo.Finally,we examined the underlying mechanism by which MA modulated redox status using a porcine intestinal epithelial cell jejunum 2(IPEC-J2)cell model in vitro.Our results demonstrated that the MA/malic enzyme 3(ME3)pathway may play an important role in reducing oxidative stress in the broiler cecum.In addition,colon infusion of MA attenuated inflammatory phenotypes in the dextran sulfate sodium salt(DSS)induced mouse colitis model.Then,dietary supplementation with controlled-release MA pellet(MAP)reduced the feed to gain(F/G)ratio and promoted chicken growth,with reduced oxidative stress and increased bacterial diver-sity.Finally,the in vitro IPEC-J2 cell model revealed that ME3 mediated the effect of MA on cellular oxidative stress.Conclusion In summary,our study firstly revealed the important role of the MA/ME3 system in the hindgut of broiler chickens for improving intestinal health and FE,which may also be crucial for the implications of colon inflammation associated diseases. 展开更多
关键词 Colitis Feed efficiency malic acid malic enzyme 3 Redox
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Assembly of Y(Ⅲ)-containing antimonotungstates induced by malic acid with catalytic activity for the synthesis of imidazoles
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作者 Guoping Yang Zhoufu Lin +5 位作者 Xize Zhang Jiawei Cao Xuejiao Chen Yufeng Liu Xiaoling Lin Ke Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2024年第12期145-148,共4页
A dimeric Y(III)-containing antimonotungstate[Y_(4)(H_(2)O)_(8)(mal)_(2)(OAc)O(Sb_(2)W_(2)^(V)W_(19)^(VI)O_(72))_(2)]^(21-)(Y_(4)mal_(2),H_(3)mal=DL-malic acid),resembling a“handshake”configuration,was synthesized a... A dimeric Y(III)-containing antimonotungstate[Y_(4)(H_(2)O)_(8)(mal)_(2)(OAc)O(Sb_(2)W_(2)^(V)W_(19)^(VI)O_(72))_(2)]^(21-)(Y_(4)mal_(2),H_(3)mal=DL-malic acid),resembling a“handshake”configuration,was synthesized and characterized.The polyanion of Y_(4)mal_(2)consists of two Dawson-derived{Y_(2)Sb_(2)W_(21)}moieties that are further linked by two mal ligands and oneμ_(2)-bridging acetate to form an asymmetric polyanion.Notably,the chiral configuration induced by the D-or L-configuration of the mal ligand results in both{Y_(2)Sb_(2)W_(21)}moieties within one polyanion exhibiting identical chirality,leading to the racemate crystallization of Y_(4)mal_(2).Moreover,Y_(4)mal_(2)exhibits excellent Lewis acid catalytic activity for environmentally friendly synthesis of imidazoles. 展开更多
关键词 POLYOXOMETALATES YTTRIUM Antimonotungstate malic acid IMIDAZOLES
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Equilibrium of Extraction of Succinic, Malic, Maleic and Fumaric Acids with Trioctylamine 被引量:7
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作者 李振宇 秦炜 +2 位作者 汪敏 黄焱 戴猷元 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2002年第3期281-285,共5页
Extraction equilibrium features of succinic acid, malic acid,maleic acid and fumaric acid were investi- gated systematically withtrioctylamine (TOA) in chloroform, 4-methyl-2-pentanone (MIBK) and1-octanol. Fourier tra... Extraction equilibrium features of succinic acid, malic acid,maleic acid and fumaric acid were investi- gated systematically withtrioctylamine (TOA) in chloroform, 4-methyl-2-pentanone (MIBK) and1-octanol. Fourier transform-infrared (FTIR) spectroscopic analysisof organic samples loaded with the acid shows that amine forms 1:1complex of ion-pair association with succinic acid, malic acid andmaleic acid, and 1:1, 2:1 complex of ion-pair association withfumaric acid. It is proposed that the complex forms depend on thesecond dissociation constant of the dibasic acid, pK_a2. 展开更多
关键词 succinic acid malic acid maleic acid fumaric acid
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Separation and Structure of Chiral S-Malic Acid Hydrate
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作者 聂晶晶 徐端钧 +1 位作者 吴景云 蒋燕南 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2002年第4期395-398,共4页
Crystals of the chiral malic acid hydrate (C_4H_6O_5·H_2O) were unexpectedlyobtained from an ethanol/water solution containing racemic D, L-malic acid and L-asparagine. Thecrystal belongs to orthorhombic space gr... Crystals of the chiral malic acid hydrate (C_4H_6O_5·H_2O) were unexpectedlyobtained from an ethanol/water solution containing racemic D, L-malic acid and L-asparagine. Thecrystal belongs to orthorhombic space group P2_12_12_1 with cell dimensions of a = 0.5576(1), b =0.9818(2), c = 1.1793(2) nm, V = 0.6455(2) nm^3, Z = 4, μ(Mo K_a) =0.152 mm^(-1), F(000) = 320, D_c= 1.565 g·cm^(-3), R=0.051, wR = 0.136 for 657 observed reflections [ I > 2σ(I) ]. Thesignificant difference in bond distances for carboxyl groups suggests that the crystal consist ofmalate anion and protonized crystalline water. This is a report for direct separation of racemicmixture, i.e., without the formation of a molecular complex of raceme with a chiral separatingreagent. 展开更多
关键词 crystal structure R-malic acid chiral compound SEPARATION H-BONDING
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不同改性剂对硫氧镁平板性能的影响
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作者 徐开胜 刘文斌 +1 位作者 张晓青 郁邦永 《混凝土与水泥制品》 2025年第1期48-52,共5页
分别研究了丙二酸、柠檬酸和苹果酸的掺量(0、0.5%、1.0%、1.5%、2.0%、2.5%)对硫氧镁平板工作性和力学性能的影响,并进行了微观机理分析。结果表明:掺入丙二酸或苹果酸基本上降低了硫氧镁水泥的凝结时间,而掺入柠檬酸延长了硫氧镁水泥... 分别研究了丙二酸、柠檬酸和苹果酸的掺量(0、0.5%、1.0%、1.5%、2.0%、2.5%)对硫氧镁平板工作性和力学性能的影响,并进行了微观机理分析。结果表明:掺入丙二酸或苹果酸基本上降低了硫氧镁水泥的凝结时间,而掺入柠檬酸延长了硫氧镁水泥的凝结时间;掺入适量丙二酸、柠檬酸或苹果酸均能提高硫氧镁水泥的抗折和抗压强度;丙二酸、柠檬酸和苹果酸能在一定程度上抑制Mg(OH)2生成,促进5·1·7相形成,从而提高基体密实度,降低孔隙率。 展开更多
关键词 硫氧镁水泥 硫氧镁平板 丙二酸 柠檬酸 苹果酸 工作性 力学性能 微观结构
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苹果酸和柠檬酸对黄梁木叶青贮品质及微生物多样性的影响
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作者 陈金钰 田汉晨 +3 位作者 刘金洋 郭勇庆 邓铭 孙宝丽 《动物营养学报》 北大核心 2025年第2期1312-1324,共13页
本试验旨在探究添加苹果酸(MA)和柠檬酸(CA)对黄梁木叶青贮品质及微生物多样性的影响。采用单因素设计方法,设置5个组,分别为空白对照组(CK组)、MAL组(添加0.5%MA)、MAH组(添加1.0%MA)、CAL组(添加0.5%CA)和CAH组(添加1.0%CA),每组设置... 本试验旨在探究添加苹果酸(MA)和柠檬酸(CA)对黄梁木叶青贮品质及微生物多样性的影响。采用单因素设计方法,设置5个组,分别为空白对照组(CK组)、MAL组(添加0.5%MA)、MAH组(添加1.0%MA)、CAL组(添加0.5%CA)和CAH组(添加1.0%CA),每组设置3个重复;青贮60 d后开袋取样测定发酵参数、营养成分、蛋白质组分、蛋白酶活性、单宁含量以及微生物多样性。结果表明:1)与CK组相比,添加不同剂量MA和CA均可显著降低黄梁木叶青贮pH、干物质损失率(DML)以及乙酸(AA)、非蛋白氮(NPN)、氨态氮(AN)和游离氨基酸氮(FAN)含量(P<0.05),显著提高乳酸(LA)、粗蛋白质(CP)和真蛋白氮(TPN)含量(P<0.05);2)与CK组相比,MAH组酸性洗涤纤维(ADF)含量显著降低(P<0.05),MAL组和MAH组可溶性碳水化合物(WSC)含量显著提高(P<0.05);3)与CK组相比,CAL组和CAH组羧基肽酶活性显著降低(P<0.05);4)与CK组相比,添加有机酸对单宁含量无显著影响(P>0.05);5)与CK组相比,各有机酸添加组厚壁菌门相对丰度显著降低(P<0.05),乳杆菌属相对丰度有所降低(P>0.05);CAH组微小杆菌属相对丰度显著提高(P<0.05),变形菌门、不动杆菌属和气单胞菌属相对丰度有所提高(P>0.05)。综上所述,MA和CA均能不同程度改善黄梁木叶青贮品质,以添加1.0%MA效果较佳。 展开更多
关键词 黄梁木叶 苹果酸 柠檬酸 青贮品质 微生物多样性
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Structural Basis for the Interaction of 14-3-3<i>β</i>with Tricarboxylic Acid Cycle Intermediate Malate
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作者 Zhiqiang Hou Lijing Su Xiaoyan Liu 《Journal of Biosciences and Medicines》 2017年第8期36-47,共12页
The protein family of 14-3-3(s) has risen to a position of higher importance as an adaptor protein in cell biology. The seven highly conserved human 14-3-3 proteins coordinate diverse cellular processes including apop... The protein family of 14-3-3(s) has risen to a position of higher importance as an adaptor protein in cell biology. The seven highly conserved human 14-3-3 proteins coordinate diverse cellular processes including apoptosis, DNA damage response, protein trafficking, and others. In liver hepatocytes, 14-3-3β binds to Ser196-phosphorilated glucose-responsive carbohydrate response element-binding protein (ChREBP) to inhibit converting excess carbohydrate to fat by regulating the nuclear/cytosol trafficking of ChREBP. Here, we report X-ray crystal structures of homodimeric mammalian 14-3-3β in its apo, Malate-bound forms. The determined apo structure was captured with one monomer in the closed state, whereas the other one had an open conformation. Strikingly, 14-3-3β binds Malate dynamically with a double-closed state, which is distinct from all previously characterized 14-3-3(s) and target ligand-binding modes. Malate docks into a first-time observed cofactor pocket located at the concaved interface of 14-3-3β helices α2, α3, α4 through mainly electrostatic and hydrogen interactions. Such a Tricarboxylic Acid Cycle intermediate Malate bond model might offer a new approach to further analyze insulin-independent 14-3-3/ChREBP pathway of de novo fat synthesis in the liver. 展开更多
关键词 Crystal Structure 14-3-3 Protein CHREBP TRANSCRIPTION Activation MALATE malic acid
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低分子量有机酸(苹果酸)对方解石-氟的吸附/沉淀反应影响
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作者 李振炫 冯添禧 +6 位作者 吴超越 张大鹏 王逸 朱珠 桂尉竣 向育斌 David DECROOCQ 《地球科学与环境学报》 CAS 北大核心 2024年第4期499-512,共14页
低分子量有机酸常对矿物的表面反应(吸附/沉淀)产生影响,从而影响矿物的溶解、矿化等过程,进而影响环境地球化学进程中元素的迁移稳定性。苹果酸作为一种广泛存在于自然界中的有机酸,是植物通过代谢过程分泌的副产品。通过批量平衡法开... 低分子量有机酸常对矿物的表面反应(吸附/沉淀)产生影响,从而影响矿物的溶解、矿化等过程,进而影响环境地球化学进程中元素的迁移稳定性。苹果酸作为一种广泛存在于自然界中的有机酸,是植物通过代谢过程分泌的副产品。通过批量平衡法开展了苹果酸对方解石-氟的吸附/沉淀反应的影响研究,旨在深入理解有机酸在地球化学过程中的作用。结果表明:①初始pH值为7.7条件下,对于低浓度氟(≤5 mg·L^(-1)),随着苹果酸浓度的升高,其对氟去除的抑制作用呈增强趋势;对于中、高浓度氟(25或60 mg·L^(-1)),氟去除主导机制为CaF 2沉淀反应,苹果酸的抑制作用对其影响不大,但其表面吸附反应导致pH值升高和钙浓度下降。②初始pH值为8.3条件下,对于低浓度氟(≤20 mg·L^(-1)),苹果酸对氟去除仍有抑制作用;苹果酸与Ca 2+的络合反应促使pH值和钙浓度上升;对于中浓度氟(60 mg·L^(-1)),氟去除主导机制为CaF 2沉淀反应,20 mg·L^(-1)苹果酸已对其产生抑制作用,随着苹果酸浓度继续升高,pH值先降后升,钙浓度持续上升,彰显了苹果酸络合反应的效应;对于高浓度氟(100 mg·L^(-1)),100 mg·L^(-1)苹果酸能极大抑制CaF 2沉淀反应,对应的pH值未超过无苹果酸时,对应的钙浓度仍低于其空白背景值,暗示了CaF 2沉淀反应的主导性。③初始pH值为8.7条件下,对于低浓度氟(≤5 mg·L^(-1)),苹果酸对氟去除的抑制作用有所减弱,但其络合反应产生的效应十分显著,导致pH值和钙浓度上升;对于高浓度氟(240 mg·L^(-1)),氟去除主导机制为CaF 2沉淀反应,该反应随着苹果酸浓度的升高而受到抑制,对应的钙浓度不断上升彰显苹果酸络合反应的效应,而pH值的下降也表明了CaF 2沉淀反应的主导性。本研究深入探讨了氟元素在方解石矿物界面上的吸附、迁移和转化过程,为理解氟的迁移稳定性提供了新的视角和理论基础,同时对富含有机酸环境中方解石矿物的稳定性评估具有重要意义,也为氟在其他矿物上的迁移转化研究提供借鉴。 展开更多
关键词 方解石 苹果酸 溶液化学 吸附 溶解 络合 沉淀
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外源有机酸对复垦土壤中重金属Cr的活化效果研究
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作者 张治国 谭雨柠 +5 位作者 郑永红 李雅婷 卢江伟 朱海东 周新伟 欧祥鹏 《金属矿山》 CAS 北大核心 2024年第1期285-292,共8页
为了探究低分子有机酸(柠檬酸和苹果酸)对Cr污染土壤中Cr形态分布的影响,以淮南市潘一矿煤矸石山周边的复垦土壤为研究对象,通过模拟不同浓度Cr污染土壤,分析柠檬酸(CA)和苹果酸(MA)对土壤中Cr赋存形态的影响机制。结果表明:(1)随着外... 为了探究低分子有机酸(柠檬酸和苹果酸)对Cr污染土壤中Cr形态分布的影响,以淮南市潘一矿煤矸石山周边的复垦土壤为研究对象,通过模拟不同浓度Cr污染土壤,分析柠檬酸(CA)和苹果酸(MA)对土壤中Cr赋存形态的影响机制。结果表明:(1)随着外源Cr浓度的增加,土壤中Cr的活性有效提高。(2)柠檬酸和苹果酸的加入均可增加土壤中可交换态Cr的占比,即Cr的有效性得到提高,且随着柠檬酸和苹果酸浓度的升高,对土壤中Cr活化效果持续上升,柠檬酸的活化效果优于苹果酸。(3)随着老化时间的延长,有机酸对Cr的活化效果会减弱,弱结合态Cr将逐渐向强结合态Cr转化。因此,土壤重金属Cr污染修复中,可以考虑选用活化效果较好的柠檬酸作为修复辅助剂,来提升土壤Cr修复效率。研究结果可为矿区复垦土壤重金属Cr污染修复提供指导。 展开更多
关键词 铬污染 柠檬酸 苹果酸 赋存形态 污染修复
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一株产L-苹果酸黑曲霉菌株的诱变筛选及发酵培养基优化 被引量:2
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作者 刘书彤 石冰冰 +4 位作者 谭奕阳 厉成伟 魏彩霞 王德培 薛鲜丽 《食品工业科技》 CAS 北大核心 2024年第8期165-173,共9页
为筛选一株产L-苹果酸能力强的黑曲霉菌株,通过紫外诱变与高浓度放线菌酮迭代诱变的方法,将野生型菌株诱变为一株产L-苹果酸能力强的黑曲霉菌株,并对其种子或发酵培养基成分进行优化。结果表明,诱变所得一株产L-苹果酸能力强的黑曲霉CGM... 为筛选一株产L-苹果酸能力强的黑曲霉菌株,通过紫外诱变与高浓度放线菌酮迭代诱变的方法,将野生型菌株诱变为一株产L-苹果酸能力强的黑曲霉菌株,并对其种子或发酵培养基成分进行优化。结果表明,诱变所得一株产L-苹果酸能力强的黑曲霉CGMCC NO.40550菌株,其摇瓶发酵时种子培养基最适葡萄糖浓度为60 g/L、最适氮源为(NH_4)_2SO_4 4.95 g/L,黑曲霉菌球形成最优转速220 r/min;发酵培养基最适葡萄糖和最适(NH_4)_2SO_4浓度分别为180 g/L和4.95 g/L,Cu SO_4·5H_2O为其生产苹果酸最佳微量元素,最适添加量为0.065 g/L。通过单因素实验的优化,优化后的培养基更有利于L-苹果酸的合成,发酵96 h时L-苹果酸产酸量达到18.15 g/L,显著提高了245%,L-苹果酸占总酸的百分比达到71.69%。本研究为L-苹果酸的工业化生产奠定基础。 展开更多
关键词 黑曲霉 紫外诱变 L-苹果酸 摇瓶发酵 培养条件
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苹果酸大米淀粉酯的制备及其对面条品质特性的改善
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作者 徐悦 马春敏 +7 位作者 付瑶 杨杨 边鑫 王冰 王艳 刘晓飞 张光 张娜 《食品工业科技》 CAS 北大核心 2024年第11期110-117,共8页
为探究不同取代度(Degree of Substitution,DS)对苹果酸大米淀粉酯理化特性及对面条品质的影响,制备不同取代度(DS=0~0.603)苹果酸大米淀粉酯,考察了苹果酸大米淀粉酯溶解度、溶胀度、糊化特性和流变特性,以及对面条蒸煮特性、质构特性... 为探究不同取代度(Degree of Substitution,DS)对苹果酸大米淀粉酯理化特性及对面条品质的影响,制备不同取代度(DS=0~0.603)苹果酸大米淀粉酯,考察了苹果酸大米淀粉酯溶解度、溶胀度、糊化特性和流变特性,以及对面条蒸煮特性、质构特性和感官特性的改善作用。结果表明,苹果酸淀粉酯的红外光谱分析显示在光谱波数约1720 cm-1处出现一个新的吸收峰。淀粉发生酯化反应后溶解度显著升高(P<0.05),但溶胀度有所下降。糊化和流变实验结果表明,低酯化淀粉(DS=0.141~0.442)的加入显著降低(P<0.05)了淀粉的峰值黏度,降低了苹果酸淀粉酯的储能模量G′和损耗模量G″,高酯化淀粉(DS=0.603)的添加不利于改善苹果酸淀粉酯的糊化和流变特性。利用相关性分析对苹果酸淀粉酯部分理化指标(溶解度、溶胀度和糊化特性)和面条的品质(蒸煮特性、质构特性和感官特性)进行了综合分析。苹果酸大米淀粉酯可以显著提升面条的整体品质,在本实验中,取代度为0.442时,小麦粉制备的面条品质较佳。 展开更多
关键词 苹果酸 酯化 大米淀粉 理化性质 面条品质
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大豆铝激活苹果酸转运家族基因GmALMT8的鉴定与功能验证
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作者 刘慧 许文静 +5 位作者 张红梅 刘晓庆 张威 王琼 朱月林 陈华涛 《植物遗传资源学报》 CAS CSCD 北大核心 2024年第6期1027-1034,共8页
鲜食风味是影响菜用大豆食味品质的关键因素,其形成与有机酸有着密切的关联,研究有机酸合成机制对于菜用大豆的品质改良具有重要的实际意义。本研究利用大豆毛状根系统,探究与苹果酸含量显著相关的候选基因GmALMT8、GmIF7GT5和GmAP在调... 鲜食风味是影响菜用大豆食味品质的关键因素,其形成与有机酸有着密切的关联,研究有机酸合成机制对于菜用大豆的品质改良具有重要的实际意义。本研究利用大豆毛状根系统,探究与苹果酸含量显著相关的候选基因GmALMT8、GmIF7GT5和GmAP在调控苹果酸含量方面的功能,结果表明:在GmALMT8-OE毛状根中,GmALMT8基因表达量与苹果酸的含量均显著高于空载对照毛状根,而GmIF7GT5和GmAP毛状根中苹果酸的含量无显著变化。鉴于已经报道的ALMT家族基因的苹果酸转运功能,推测大豆中GmALMT8基因可能具有相似的功能,在调控苹果酸含量方面发挥重要作用。为验证GmALMT8-OE毛状根中苹果酸含量的变化是否由GmALMT8基因表达的改变所引起,本研究采用蘸花法在拟南芥中过表达GmALMT8基因。与阳性毛状根中苹果酸测定的结果相类似,过表达GmALMT8显著提高了T2代转基因拟南芥株系种子中的苹果酸含量,进一步证明GmALMT8的稳定表达能够提高苹果酸含量,明确GmALMT8基因在大豆中具有调控苹果酸含量的生物学功能,丰富了大豆有机酸的理论研究,对菜用大豆优质育种具有参考价值。 展开更多
关键词 菜用大豆 苹果酸 候选基因 功能分析
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