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Plant Growth Promoting Rhizobacteria Having 1-Aminocyclopropane-1-Carboxylic Acid Deaminase to Induce Salt Tolerance in Sunflower (<i>Helianthus annus L.</i>)
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作者 Muhammad Zahid Kiani Arshad Ali +2 位作者 Tariq Sultan Rizwan Ahmad Syed Ishtiaq Hydar 《Natural Resources》 2015年第6期391-397,共7页
Soil salinity badly affects agriculture productivity through accumulation of salts in upper layers of soils. The harmful effects of salts in arable lands have influenced modern as well as ancient civilizations. A pot ... Soil salinity badly affects agriculture productivity through accumulation of salts in upper layers of soils. The harmful effects of salts in arable lands have influenced modern as well as ancient civilizations. A pot study was carried out to test the performance of two PGPR isolates (KS 8, KS 28) on sunflower (SMH-0917) under different salinity levels (8, 10 and 12 dS·m-1). These salinity levels were developed by adding calculated amount of salts (NaCl, Na2SO4, CaCl2 and MgSO4) with ratio of 3:4:2:1. The bacterial strains KS 8 and KS 28 were applied separately in two treatments while third treatment was co-inoculation (KS mix). Completely randomized experimental design (CRD) was used and data were collected at flowering stage about pre-decided plant growth parameters (plant height, shoot dry weight and root dry weight). The bacterial isolate KS 8 showed an increase of 26, 102% and 83% in plant height, shoot dry weight and root dry weight at EC 8 dS·m-1, while this improvement was 67%, 163% and 296% at EC 10 dS·m-1, however an increase of 100%, 74% and 382% was recorded over control respectively at EC 12 dS·m-1. Similarly isolate KS 28 exhibited an increase of 14%, 69% and 54% in plant height;shoot dry weight and root dry weight at EC 8 dS·m-1, whereas this improvement was 56%, 163% and 188% at EC 10 dS·m-1, while an increase of 60%, 41% and 282% was registered respectively over control at EC 12 dS·m-1. The increase due to mixture treatments was 4%, 41% and 16% in plant height, shoot dry weight and root dry weight at EC 8 dS·m-1, while an increase of 33%, 57% and 100% at EC 10 dS·m-1, whereas an improvement of 53%, 33% and 164% respectively was noted at EC 12 dS·m-1 over un-inoculated. The isolate KS 8 performed better than KS 28 and mixture treatment. These two PGPR strains could be used to mitigate the adverse impact caused by salinity stress on sunflower. 展开更多
关键词 Plant Growth Promoting RHIZOBACTERIA Strains 1-aminocyclopropane-1-carboxylic Acid (acc) DEAMINASE Salinity
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小苍兰ACC合成酶FhACS1基因的克隆与序列分析 被引量:1
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作者 袁媛 王月 +1 位作者 唐东芹 连芳青 《植物研究》 CAS CSCD 北大核心 2011年第4期422-428,共7页
以小苍兰品种"上农金皇后"为研究对象,利用PCR技术和染色体步移技术首次克隆到了ACC合成酶FhACS1基因的全长序列和编码序列。结果表明:FhACS1基因全长为2 576 bp,包含长为433 bp的5′端非编码区序列(5′-UTR)以及长为373 bp的... 以小苍兰品种"上农金皇后"为研究对象,利用PCR技术和染色体步移技术首次克隆到了ACC合成酶FhACS1基因的全长序列和编码序列。结果表明:FhACS1基因全长为2 576 bp,包含长为433 bp的5′端非编码区序列(5′-UTR)以及长为373 bp的3′端非编码区序列(3-′UTR);开放读码框(ORF)长度为1 371 bp,推定编码457个氨基酸。分析表明,该基因包含3个内含子和4个外显子。序列分析结果显示,FhACS1推导蛋白具备ACS蛋白的7个保守结构域;在氨基酸水平上,FhACS1与小果芭蕉的同源性最高(85%);系统进化分析表明,FhACS1与孟宗竹BaACS(BAC56949.1)、水稻OsACS1(AAA33888.1)、小果芭蕉MaACS1(AAQ13435)的亲缘关系最近。在其已知启动子区域,发现有多个对脱落酸、赤霉素、细胞分裂素等激素响应的顺式元件,以及对干旱和低温等逆境胁迫响应的顺式元件。 展开更多
关键词 小苍兰 acc合成酶 基因 序列分析 顺式元件
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Isolation of a Tomato Protease that May Be Involved in Proteolysis of 1-Aminocyclopropane-l-Carboxylate Synthase 被引量:3
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作者 Jian-Feng LI Liang-Hu QU Ning LI 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2005年第10期1220-1227,共8页
1-aminocyclopropane- 1-carboxylate (ACC) synthase is a principal enzyme that catalyses the committed step in phytohormone ethylene biosynthesis. Previous evidence indicates that the hypervariable C-terminus of ACC s... 1-aminocyclopropane- 1-carboxylate (ACC) synthase is a principal enzyme that catalyses the committed step in phytohormone ethylene biosynthesis. Previous evidence indicates that the hypervariable C-terminus of ACC synthase is most likely to be processed proteolytically in vivo. However, the protease responsible has not been identified thus far. In the present study, we detected proteolytic activity against ACC synthase (LeACS2) in tomato (Lycopersicon esculentum Mill.) fruit extract based on a newly established in vitro assay system. Purification of the protease through DEAE, gel filtration and MonoQ chromatography resulted in considerable enrichment of a 64-kDa protein species. Subsequent biochemical analysis of the purified tomato protease revealed that the optimal conditions for its proteolytic activity were at pH 8.0 and at 37 ~C. In addition, the protease activity was blocked completely by the metalloprotease inhibitor 1,10-phenanthroline. The present study represents the first report on the isolation of an ACC synthase- processing protease from plant tissues. 展开更多
关键词 1-aminocyclopropane-1-carboxylate (acc synthase biochemical analysis C-terminalproteolysis ISOLATION protease.
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Ethylene Production and 1-Aminocyclopropane-l-Carboxylate (ACC) Synthase Gene Expression in Tomato ( L ycopsicon esculentum Mill.) Leaves Under Enhanced UV-B Radiation 被引量:2
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作者 Lizhe An Xiaofeng Xu +7 位作者 Hongguan Tang Manxiao Zhang Zongdong HOU Yanhong Liu Zhiguang Zhao Huyuan Feng Shijian Xu Xunling Wang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2006年第10期1190-1196,共7页
Tomato (Lycopslcon esculentum Mill.) plants grown in a greenhouse were irradiated with two different levels of UV-B, namely 8.82 (T1) and 12.6 kJ/m^2 per day (T2). Ethylene production, 1-aminocyclopropane-1-carb... Tomato (Lycopslcon esculentum Mill.) plants grown in a greenhouse were irradiated with two different levels of UV-B, namely 8.82 (T1) and 12.6 kJ/m^2 per day (T2). Ethylene production, 1-aminocyclopropane-1-carboxylate (ACC) content, 1-(malonylamino) cyclopvopane-1-carboxylic acid (MACC) content, gene expression of ACC aynthase (EC 4.4.1.14), and ACC oxidase activity in tomato leaves were determined. The results Indicated that ACC content, the activity of ACC synthase and ACC oxidase, and ethylene production Increased continuously under low doses of UV-B radiation, whereas at high doses of radiation these parameters Increased during the first 12 d and then started to decrease. The MACC content increased continuously over 18 d under both doses of UV-B irradiation. The changes in ACC content, ACC synthaae activity, ACC oxidase activity, the transcriptional level of the ACC synthase gene, and ethylene production were consistent with each other, suggesting that ACC synthase was the key enzyme in ethylene biosynthesis and that ethylene production in tomato leaf tissues under UV-B radiation could be regulated by the expression of the ACC synthase gene. The results also indicate that the change in ethylene metabolism may be an adaptive mechanism to enhanced UV-B radiation. 展开更多
关键词 enhanced UV-B radiation ethylene production gene expression of 1-aminocyclopropane-l-carboxylate (acc synthase Lycopsicon esculentum
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丙烯和1-MCP处理对采后柿果实ACS和ACO基因表达的影响 被引量:12
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作者 刘乐 饶景萍 +1 位作者 常晓晓 弋顺超 《中国农业科学》 CAS CSCD 北大核心 2009年第6期2092-2097,共6页
【目的】研究丙烯、1-甲基环丙烯(1-MCP)处理对采后柿果实中与乙烯合成相关的ACS、ACO基因特异表达的影响。【方法】以中国涩柿的优良品种‘富平尖柿’为试材,于初熟期采收后将果实分别用丙烯、1-MCP处理,在常温下贮藏,定期检测乙烯释... 【目的】研究丙烯、1-甲基环丙烯(1-MCP)处理对采后柿果实中与乙烯合成相关的ACS、ACO基因特异表达的影响。【方法】以中国涩柿的优良品种‘富平尖柿’为试材,于初熟期采收后将果实分别用丙烯、1-MCP处理,在常温下贮藏,定期检测乙烯释放速率及分组织提取RNA进行Northern分析。【结果】丙烯处理促进ACS、ACO基因表达进而促进内源乙烯合成;1-MCP处理抑制ACS、ACO基因的表达从而抑制内源乙烯合成。不过,二者对ACS、ACO基因表达的作用效果在不同组织中差异较大:1-MCP处理对ACS、ACO基因表达的抑制作用在果皮中最明显,其次是果肉、果心部位,果蒂着生部位处最低;丙烯对ACS、ACO基因表达的促进作用表现为果肉、果心、果皮、果蒂着生部位递增。另外,ACS、ACO基因家族各成员在不同组织的表达也不同,DKACS3基因只在果蒂着生部位表达在其它组织中没有表达,DKACS2基因在丙烯处理果中的4个组织中均有表达。【结论】丙烯处理促进ACS、ACO基因表达,1-MCP处理抑制ACS、ACO基因的表达;ACS、ACO基因在不同组织中的表达差异较大;ACS、ACO基因家族各成员在不同组织中的表达也不同。 展开更多
关键词 丙烯 1-MCP acc合成酶 acc氧化酶
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Mutation in the gene encoding 1-aminocyclopropane-1-carboxylate synthase 4 (CitACS4) led to andromonoecy in watermelon 被引量:1
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作者 Gaojie Ji Jie Zhang +9 位作者 Haiying Zhang Honghe Sun Guoyi Gong Jianting Shi Shouwei Tian Shaogui Guo Yi Ren Huolin Shen Junping Gao Yong Xu 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2016年第9期762-765,共4页
Summary Although it has been reported previously that ethylene plays a critical role in sex determination in cucurbit species, how the andromonoecy that carries both the male and hermaphroditic flowers is determined i... Summary Although it has been reported previously that ethylene plays a critical role in sex determination in cucurbit species, how the andromonoecy that carries both the male and hermaphroditic flowers is determined in watermelon is still unknown. Here we showed that the watermelon gene 1-aminocyclopropane-1-carboxylate syn- thase 4 CCitACS4), expressed specifically in carpel primor- dia, determines the andromonoecy in watermelon. Among four single nucleotide polymorphism (SNPs) and one lnDel identified in the coding region of CitACS4, the C364W mutation located in the conserved box 6 was co- segregated with andromonoecy. Enzymatic analyses showed that the C364W mutation caused a reduced activity in CitACS4. We believe that the reduced CitACS4 activity may hamper the programmed cell death in stamen primordia, leading to the formation of hermaphroditic flowers. 展开更多
关键词 1-aminocyclopropane-1-carboxylic acid synthase Citrullus lanatus sex determination
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大豆1-氨基环丙烷-1-羧酸合酶顺式天然反义转录物的分析鉴定
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作者 刘明 杨君 安利佳 《生物工程学报》 CAS CSCD 北大核心 2008年第12期2131-2132,共2页
1-氨基环丙烷-1-羧酸合酶(1-aminocyclopropane-1-carboxylate synthase,ACS)是植物乙烯生物合成途径中的关键酶,催化了乙烯生物合成中由S-腺苷蛋氨酸(S-adenosyl-L-methionine,SAM)转化为1-氨基环丙烷-1-羧酸(1-aminocyclopropane-1-ca... 1-氨基环丙烷-1-羧酸合酶(1-aminocyclopropane-1-carboxylate synthase,ACS)是植物乙烯生物合成途径中的关键酶,催化了乙烯生物合成中由S-腺苷蛋氨酸(S-adenosyl-L-methionine,SAM)转化为1-氨基环丙烷-1-羧酸(1-aminocyclopropane-1-carboxylate,ACC)这一限速步骤。ACC合酶由多基因家族编码,在转录及转录后水平上受到多种生物和非生物因素的差异调节,其表达调节机制复杂,尚未完全清楚。最近的研究揭示,在植物中发现的一些天然反义转录物(Natural antisense transcripts,NATs)在基因表达调节机制中发挥了不可忽视的作用,因而天然反义转录物的研究受到了广泛的关注。本研究利用RT-PCR法在6种中国东北大豆中克隆出一种ACC合酶基因天然反义转录物,序列测定结果表明这是一种顺式天然反义转录物(cis-NAT),命名为ASACS2。实时定量RT-PCR(Real-time RT-PCR)测定结果表明,ASACS2与其高丰度表达的正义转录物SACS2伴随表达,并且在营养生长期得到了积累。令人感兴趣的是,6个大豆品种中ASACS2和SACS2的表达量保持一定比例,且表现出品种特异性。目前的研究工作揭示了一种新的NATs可能参与的乙烯生物合成的调控机制,为转基因育种和植物发育调控研究提供了新的思路。 展开更多
关键词 1-氨基环丙烷-1-羧酸(acc)合酶 天然反义转录物 大豆 实时定量RT-PCR
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番茄ACC合成酶cDNA克隆及其对果实成熟的反义抑制 被引量:31
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作者 刘传银 田颖川 +5 位作者 沈全光 蒋浩 鞠戎 阎田 刘存德 莽克强 《生物工程学报》 CAS CSCD 北大核心 1998年第2期139-146,共8页
利用RTPCR技术克隆了ACC合成酶多基因家族成员之一LEACC2编码区约17kb的cDNA,经酶切图谱和序列分析鉴定无误后,反向插入到植物表达载体pBin437中,构建了表达ACC合成酶反义RNA的二元载体。... 利用RTPCR技术克隆了ACC合成酶多基因家族成员之一LEACC2编码区约17kb的cDNA,经酶切图谱和序列分析鉴定无误后,反向插入到植物表达载体pBin437中,构建了表达ACC合成酶反义RNA的二元载体。经农杆菌途径转化番茄“丽春”品种后,通过PCR检测从抗卡那霉素再生植株中筛选到6株转基因植株,Southern杂交确证了外源基因是以单拷贝插入到番茄染色体中;对果实乙烯释放的测定结果表明转基因番茄果实的乙烯释放量仅为对照的30%左右,在室温下转基因番茄果实采后保存60d以上仍然没有变红、软化。以上结果表明其反义RNA在转基因番茄中的表达能有效地抑制乙烯的生物合成从而延缓果实成熟,表现出良好的耐储保鲜特性。对转基因植株子一代(T1)的分析结果进一步表明反义ACC合成酶基因以典型的单基因方式传到子代。通过对子二代的分析已初步筛选到一个耐储藏的转基因番茄纯合品系。 展开更多
关键词 acc 合成酶 反义RNA 转基因 番茄 果帝成熟
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番茄ACC合成酶基因的反义RNA-核酶嵌合基因植物表达载体的构建及对番茄的转化 被引量:11
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作者 张晓海 扈廷茂 +2 位作者 海燕 李丽莉 王永胜 《内蒙古大学学报(自然科学版)》 CAS CSCD 北大核心 2001年第1期74-78,共5页
将克隆的番茄 ACC合成酶基因的反义 RNA-核酶嵌合的 DNA序列用 Hind 和 Kpn I切割后重组于植物表达载体 p GA643中 ,用三亲融合法导入农杆菌 LBA4 40 4中 ,采用叶盘法转化番茄子叶 ,诱导出再生小植株 ,获得了卡那霉素的抗性植株 .提取... 将克隆的番茄 ACC合成酶基因的反义 RNA-核酶嵌合的 DNA序列用 Hind 和 Kpn I切割后重组于植物表达载体 p GA643中 ,用三亲融合法导入农杆菌 LBA4 40 4中 ,采用叶盘法转化番茄子叶 ,诱导出再生小植株 ,获得了卡那霉素的抗性植株 .提取植物总 DNA,用p GA643作探针 ,通过斑点杂交 ,已筛选出整合有外源基因的工程植株 .为进一步研究该嵌合基因对 ACC合成酶基因表达的影响及获得商品化的转基因番茄奠定了基础 . 展开更多
关键词 转基因番茄 acc合成酶 反义RNA 核酶 转化
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不同性别类型黄瓜ACC合酶基因的单核苷酸多态性标记和酶切扩增长度多态性标记 被引量:14
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作者 向太和 王利琳 +3 位作者 庞基良 胡江琴 申屠连峰 吴锴 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2006年第4期362-367,共6页
黄瓜的性别分化与乙烯密切相关,1-氨基环丙烷-1-羧酸(ACC)合酶是乙烯生物合成过程中的关键酶.根据ACC合酶基因家族的保守序列设计PCR引物,从8个不同性别类型(雌雄同株、强雌性和全雌性)黄瓜品种中克隆了长度为1188bp的ACC合酶基因(CS-AC... 黄瓜的性别分化与乙烯密切相关,1-氨基环丙烷-1-羧酸(ACC)合酶是乙烯生物合成过程中的关键酶.根据ACC合酶基因家族的保守序列设计PCR引物,从8个不同性别类型(雌雄同株、强雌性和全雌性)黄瓜品种中克隆了长度为1188bp的ACC合酶基因(CS-ACS2)片段(GenBank登记号为:DQ115884~DQ115886和DQ115875~DQ115879).经测序分析,3个雌雄同株性别类型品种的序列完全相同.与之相比,5个强雌性和全雌性品种中存在8个单核苷酸多态性(SNPs)标记,SNPs标记为4个A←→G和4个T←→C之间的转换.在8个SNPs中,有1个SNP位于内含子区域,其余7个SNPs都位于外显子区域.在7个位于外显子区域的SNPs中,有3个为非编码区的SNPs,4个为cSNPs.而在4个cSNPs中,有3个导致了编码的氨基酸序列改变.研究结果表明,与雌雄同株性别类型相比,雌性系中均存在单核苷酸的变异,这提示ACC合酶基因CS-ACS2的单核苷酸变异可能与黄瓜雌性系的发生形成有关.另一方面,根据SNP多态性还发展了一个酶切扩增长度多态性(CAPS)标记C-MT700.利用CAPS标记C-MT700能将强雌性优良品种MT-705与其他黄瓜品种相区别,该标记在黄瓜育种生产上具有一定的应用价值.此外,研究获得的SNPs标记和CAPS标记丰富了黄瓜的分子标记种类. 展开更多
关键词 黄瓜 性别类型 1-氨基环丙烷-1-羧酸(acc)合酶基因 单核苷酸多态性(SNP) 酶切扩增长度多态性(CAPS)
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植物ACC合成酶的分子生物学 被引量:4
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作者 万小荣 李玲 《安徽农业科学》 CAS 北大核心 2007年第3期654-655,共2页
论述了ACC合成酶的分子生物学研究进展,阐述了系统1乙烯和系统2乙烯形成过程中ACC合成酶基因的表达特点。
关键词 acc合成酶 系统1乙烯 系统2乙烯
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Quinclorac Resistance in Echinochloa crus-galli from China 被引量:4
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作者 PENG Qiong HAN Heping +3 位作者 YANG Xia BAI Lianyang YU Qin Stephen BPOWLES 《Rice science》 SCIE CSCD 2019年第5期300-308,共9页
Echinochloa crus-galli is a major weed in rice fields in China,and quinclorac has been long used for its control.Over-reliance of quinclorac has resulted in quinclorac resistance in E.crus-galli.Two resistant(R)E.crus... Echinochloa crus-galli is a major weed in rice fields in China,and quinclorac has been long used for its control.Over-reliance of quinclorac has resulted in quinclorac resistance in E.crus-galli.Two resistant(R)E.crus-galli populations from Hunan,China were confirmed to be at least 78-fold more resistant to quinclorac than the susceptible(S)population.No difference in foliar uptake of 14C-labelled quinclorac was detected between the R and S plants.However,a higher level of 14C translocation and a lower level of quinclorac metabolism were found in the R plants.Basal and induced expression levels ofβ-cyanoalanine synthase(β-CAS)gene andβ-CAS activity were not significantly different between the R and S plants.However,the induction expression of 1-aminocyclopropane-1-carboxylic acid oxidase(ACO1)gene by quinclorac treatment was evident in the S plants but not in the R plants.Quinclorac resistance in the two resistant E.crus-galli populations was not likely to be related to foliar uptake,translocation or metabolism of quinclorac,nor to cyanide detoxification viaβ-CAS.Thus,target-site based quinclorac signal reception and transduction and regulation of the ethylene synthesis pathway should be the focus for further research. 展开更多
关键词 ECHINOCHLOA crus-galli QUINCLORAC RESISTANCE QUINCLORAC metabolism β-cyanoalanine synthase 1-aminocyclopropane-1-carboxylic ACID synthase 1-aminocyclopropane-1-carboxylic ACID OXIDASE rice
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The Dependence of <i>N</i>-Malonyltryptophan Formation in Plants on Water Deficit (Review)
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作者 Kim Z. Gamburg 《Natural Science》 2021年第2期26-41,共16页
Drought stress in plants is accompanied by several metabolic changes. One of them is the appearance of <em>N</em>-malonyltryptophan (MT) during leaf wilting of many species, but there is a significant numb... Drought stress in plants is accompanied by several metabolic changes. One of them is the appearance of <em>N</em>-malonyltryptophan (MT) during leaf wilting of many species, but there is a significant number of plant species in which the appearance of MT did not occur. Plants of some species were able to synthesize also <em>N</em>-acetyltryptophan (AT). Excised tomato leaves incubated with D-amino acids (including D-Trp) transform them into malonyl- and acetyl-derivatives even without water deficit. However, MT which appeared during water deficit has been shown to contain L-Trp. Amino acid—1-amino-cyclopropane-1-carboxylic acid (ACC) is also malonylated during water deficit, but other L-amino acids were not malonylated. <em>N</em>-malonyl transferases specific for Trp and ACC have been found in several plants. The existence of <em>N</em>-malonyltransferase specific to L-Trp and appeared during water deficit in plants forming MT is supposed, but clear experimental proof has not been obtained yet. Plants can transform MT applied exogenously into Trp and further to indole-3-acetic acid (IAA). But no evidence has been appeared up to now that endogenous MT may be a source of IAA. It is unknown till now why it is necessary for plants of many species to malonylate only Trp during water deficit. How MT metabolized in animals and if it affects them is also unknown. The necessity to use molecular-genetic approaches for the elucidation of the physiological significance of MT formation during water deficit is underlined. 展开更多
关键词 Drought Stress N-Acetyltryptophan 1-aminocyclopropane-1-carboxylic Acid Indole-3-Acetic Acid Tryptophan Malonylation
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粉蕉MbACS7基因的克隆及表达分析
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作者 符思颖 李美英 +3 位作者 颜彦 田丽波 商桑 胡伟 《分子植物育种》 CAS 北大核心 2023年第16期5247-5254,共8页
乙烯合成及其效应是决定香蕉果实成熟的核心要素,其中1-氨基环丙烷-1-羧酸(ACC)合成酶(ACS)是乙烯合成途径的限速酶。粉蕉果实成熟速度较快,保鲜难度较大。研究粉蕉ACS家族基因的特征和表达模式可为控制香蕉果实成熟进程和延长货架期提... 乙烯合成及其效应是决定香蕉果实成熟的核心要素,其中1-氨基环丙烷-1-羧酸(ACC)合成酶(ACS)是乙烯合成途径的限速酶。粉蕉果实成熟速度较快,保鲜难度较大。研究粉蕉ACS家族基因的特征和表达模式可为控制香蕉果实成熟进程和延长货架期提供理论依据。本研究从粉蕉中克隆获得一个全长序列为1458 bp的目的片段,编码485个氨基酸,分子量为54.751 kD,具有PLN02450保守结构域(37~1377氨基酸),属于ACS基因家族蛋白,因此被命名为MbACS7。理化性质分析表明MbACS7蛋白亲水且不稳定。进化分析表明MbACS7蛋白预测的氨基酸序列与苦瓜(Momordica charantia)ACS蛋白的氨基酸序列(CAE53271.1)遗传关系较近。瞬时表达分析表明MbACS7蛋白在烟草表皮细胞的细胞核中强烈表达,表明该蛋白可能在细胞核中发挥着重要的生理功能。实时荧光定量表达分析表明MbACS7基因在粉蕉果实成熟期表达量最高,为果实发育初期的900多倍。本研究为进一步解析MbACS7基因在粉蕉果实乙烯生物合成中的功能奠定基础,也为改良香蕉果实贮藏性提供基因资源。 展开更多
关键词 粉蕉 1-氨基环丙烷-1-羧酸合成酶(ACS) 乙烯生物合成 表达分析
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余甘子鞣质对代谢相关脂肪性肝病小鼠脂质代谢及肠道菌群的调节作用 被引量:8
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作者 张艳鹤 郑亚云 +4 位作者 芦超 常文娟 靳菲菲 李锦秀 张超 《药物评价研究》 CAS 2022年第2期287-293,共7页
目的研究余甘子Phyllanthus emblica L.鞣质对代谢相关脂肪性肝病(MAFLD)小鼠脂质代谢及肠道菌群的调节作用。方法将C57BL/6小鼠随机分为对照组、模型组和余甘子鞣质低、高剂量(200、400 mg·kg^(−1))组及非诺贝特(阳性药,50 mg... 目的研究余甘子Phyllanthus emblica L.鞣质对代谢相关脂肪性肝病(MAFLD)小鼠脂质代谢及肠道菌群的调节作用。方法将C57BL/6小鼠随机分为对照组、模型组和余甘子鞣质低、高剂量(200、400 mg·kg^(−1))组及非诺贝特(阳性药,50 mg·kg^(−1))组,每组10只。对照组小鼠常规饲料喂养,其余各组小鼠均给予高脂饲料喂养,建立MAFLD小鼠模型;ig给予相应药物干预,对照组及模型组给予同体积生理盐水,每天1次,连续给药8周。处死小鼠,收集血液、肝脏、粪便。计算肝脏系数;HE染色法观察肝组织病理学变化;试剂盒法检测小鼠血清中丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、三酰甘油(TG)、总胆固醇(TC)含量;实时荧光定量PCR(qRT-PCR)及Western blotting法检测肝组织中固醇调节元件结合蛋白(SREBP-1)、脂肪酸合成酶(FASN)、乙酰辅酶A羧化酶(ACC)mRNA和蛋白表达量;PCR扩增法检测实验前后小鼠粪便双歧杆菌、乳酸杆菌的含量变化。结果与模型组比较,低、高剂量余甘子鞣质干预后小鼠肝脏系数显著降低(P<0.05、0.01),小鼠肝组织脂肪变程度减轻;小鼠血清中ALT、AST、TG、TC水平均显著降低(P<0.05、0.01);肝组织中SREBP-1、FASN、ACC mRNA和蛋白水平均显著降低(P<0.05、0.01);粪便中双歧杆菌、乳酸杆菌的含量显著升高(P<0.01)。结论余甘子鞣质能够通过SREBP-1/FASN/ACC通路调节脂质代谢、改善肠道菌群平衡,改善MAFLD。 展开更多
关键词 余甘子 鞣质 代谢相关脂肪性肝病 肠道菌群 固醇调节元件结合蛋白(SREBP-1) 脂肪酸合成酶(FASN) 乙酰辅酶A羧化酶(acc)
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Exogenous ethylene influences flower opening of cut roses (Rosa hybrida) by regulating the genes encoding ethylene biosynthesis enzymes 被引量:20
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作者 MA Nan1, CAI Lei1, LU Wangjin2, TAN Hui1 & GAO Junping1 1. Department of Ornamental Horticulture and Landscape Architecture, China Agricultural University, Beijing 100094, China 2. Department of Horticulture, South China Agricultural University, Guangzhou 510642,China 《Science China(Life Sciences)》 SCIE CAS 2005年第5期434-444,共11页
The purpose of this paper is to investigate the differential responses of flower opening to ethylene in two cut rose cultivars, ‘Samantha’, whose opening process is promoted, and ‘Kardinal’, whose opening process ... The purpose of this paper is to investigate the differential responses of flower opening to ethylene in two cut rose cultivars, ‘Samantha’, whose opening process is promoted, and ‘Kardinal’, whose opening process is inhibited by ethylene. Ethylene production and 1- aminocyclopropane-1-carboxylate (ACC) synthase and oxidase activities were determined first. After ethylene treatment, ethylene production, ACC synthase (ACS) and ACC oxidase (ACO) activities in petals increased and peaked at the earlier stage (stage 3) in ‘Samantha’, and they were much more dramatically enhanced and peaked at the later stage (stage 4) in ‘Kardinal’ than control during vasing. cDNA fragments of three Rh-ACSs and one Rh- ACO genes were cloned and designated as Rh-ACS1, Rh-ACS2, Rh-ACS3 and Rh-ACO1 respectively. Northern blotting analysis revealed that, among three genes of ACS, ethylene-in- duced expression patterns of Rh-ACS3 gene corresponded to ACS activity and ethylene production in both cultivars. A more dramatic accumulation of Rh-ACS3 mRNA was induced by ethylene in ‘Kardinal’ than that of ‘Samantha’. As an ethylene action inhibitor, STS at concentration of 0.2 mmol/L generally inhib-ited the expression of Rh-ACSs and Rh-ACO in both cultivars, although it induced the expression of Rh-ACS3 transiently in ‘Kardinal’. Our results suggests that ‘Kardinal’ is more sensitive to ethylene than ‘Samantha’; and the changes of Rh-ACS3 expression caused by ethylene might be related to the acceleration of flower opening in ‘Samantha’ and the inhibition in ‘Kardinal’. Additional results indicated that three Rh-ACSs genes were differentially associated with flower opening and senescence as well as wounding. 展开更多
关键词 cut rose (Rosa hybrida) FLOWER opening ethylene 1-aminocyclopropane-1-carboxylic acid (acc) acc synthase (ACS) acc OXIDASE (ACO) gene expression.
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