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植物硒代谢积累及相关酶的研究进展 被引量:25
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作者 杜玉潇 李亚男 陈大清 《热带亚热带植物学报》 CAS CSCD 北大核心 2007年第3期269-276,共8页
阐述了植物硒代谢的基本途径及其积累的分子机制,详细介绍了几种参与硒代谢的关键性酶的分子生物学特性。并展望了有关植物硒代谢的发展趋势。
关键词 植物 代谢 ATP硫酸化酶 谷光甘肽过氧化物酶 硒代半胱氨酸甲基转移酶 综述
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Selenocysteine methyltransferase SMT catalyzed the synthesis of Se-methylselenocysteine to regulate the accumulation of glucosinolates and sulforaphane in broccoli
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作者 Qi Wu Junwei Wang +4 位作者 Yuxiao Tian Chunyan Zhou Shuxiang Mao Qiuyun Wu Ke Huang 《Horticultural Plant Journal》 SCIE CAS CSCD 2024年第5期1151-1164,共14页
Selenocysteine methyltransferase(SMT)is a key enzyme involved in the Se metabolism pathway,and it is responsible for the catalysis of Se-methylselenocysteine(SeMSC)compound formation.Previous studies showed that selen... Selenocysteine methyltransferase(SMT)is a key enzyme involved in the Se metabolism pathway,and it is responsible for the catalysis of Se-methylselenocysteine(SeMSC)compound formation.Previous studies showed that selenium treatment activated SMT expression and promoted the accumulation of glucosinolates(GSLs)and sulforaphane,but the roles and functional mechanisms of SMT in mediating GSLs and sulforaphane synthesis remain unclear.In this study,we identified the BoSMT gene in broccoli and uncovered its roles in mediating GSLs biosynthesis.Transgenic assays revealed that BoSMT is involved in SeMSC biosynthesis in broccoli.More importantly,the contents of GSLs and sulforaphane were significantly increased in the BoSMT-overexpressing broccoli lines but decreased in the knockdown lines,suggesting that BoSMT played a positive role in regulating GSLs and sulforaphane synthesis.Further evidence indicated that BoSMT-mediated overaccumulation of GSLs and sulforaphane might be due to the increase in the endogenous SeMSC content.Compared with the mock(water)treatment,selenite-induced significantly increases of the SeMSC content in the BoSMT-knockdown plants partially compensated the phenotype of GSLs and sulforaphane loss.Compared with the mock treatment,exogenous SeMSC treatment significantly increased the contents of GSL and sulforaphane and activated GSL synthesis-related gene expression,suggesting that SeMSC acted as a positive regulator for GSL and sulforaphane production.Our findings provided novel insights into selenium-mediated GSLs and sulforaphane accumulation.The genetic manipulation of BoSMT might be a useful strategy for improving the dietary nutritional values of broccoli. 展开更多
关键词 selenocysteine methyltransferase Transgenic broccoli Se-methylselenocysteine Glucosinolate sulforaphane Selenium
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Quantitative Analysis of ATP Sulfurylase and Selenocysteine Methyltransferase Gene Expression in Different Organs of Tea Plant (<i>Camellia sinensis</i>) 被引量:3
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作者 Shaoqiang Tao Juan Li +4 位作者 Xungang Gu Yanan Wang Qiang Xia Bing Qin Lin Zhu 《American Journal of Plant Sciences》 2012年第1期51-59,共9页
Tea plant (Camellia sinensis) has unique biological features for the study of cellular and molecular mechanisms, an evergreen broad-leaved woody plant which can accumulate selenium in soil abundant of Selenium. Expres... Tea plant (Camellia sinensis) has unique biological features for the study of cellular and molecular mechanisms, an evergreen broad-leaved woody plant which can accumulate selenium in soil abundant of Selenium. Expression of the genes related to Selenium (Se) metabolism is an adaptation to the soil environment for a long period. The purpose of the present study was to explore if there exist differences of expression about these genes in tea plant between growing in Selenium-abundant and normal soil. A quantitative real-time reverse transcription polymerase chain reaction (Q-RT-PCR) assay was done for quantification of ATP sulfurylase (APS) and selenocysteine methyltransferase (SMT) mRNA normalized to Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene in tea plant. Young leaves, mature leaves and tender roots from tea plants growing in soil abundant of Selenium were respectively obtained from Shitai County, Anhui Province, and also the relevant materials of the selenium un-enriched tea plant planted at agricultural garden of Ahui Agriculture University were taken as control for real-time PCR analysis. The results showed that APS1, APS2 and SMT expression levels for either young or mature leaves in selenium-enriched tea plant were lower than that in ordinary (selenium un-enriched) tea plant. In contrast, the APS1, APS2 and SMT expression level of roots in selenium-enriched tea plant were all higher than that in ordinary tea plant. APS1 gene expression level of roots in selenium-enriched tea plant was about 1.6 times higher than that in the ordinary tea plant, APS2 gene expression level was about 4.8-fold higher than that in the ordinary tea plant, SMT gene expression level was about 3.3 times higher than that in the ordinary tea plant. Among various tissues of selenium-enriched tea plant, APS1 gene relative expression level of young leaves was similar to or slightly higher than mature leaves, and the one of roots was the lowest among them;APS2 gene relative expression level of young leaves was similar to or slig 展开更多
关键词 Quantitative Real-Time Polymerase Chain Reaction ATP Sulfurylase selenocysteine methyltransferase Tea Plant (Camellia sinensis)
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过表达硒代半胱氨酸甲基转移酶烟草的硒耐受特性分析 被引量:2
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作者 白日巧 陈大清 +3 位作者 龙永豪 姚新 杜玉萧 李亚男 《仲恺农业工程学院学报》 CAS 2018年第1期15-19,共5页
以经鉴定的硒代半胱氨酸甲基转移酶(Selenocysteine methyltransferase,SMT)转基因烟草(Nicotiana tabacum L)和野生型烟草(NC89)为材料,置于添加不同质量浓度(0、20、40和60 mg/L)硒酸钠的MS培养基上进行培养,35 d后分别测定两种处理... 以经鉴定的硒代半胱氨酸甲基转移酶(Selenocysteine methyltransferase,SMT)转基因烟草(Nicotiana tabacum L)和野生型烟草(NC89)为材料,置于添加不同质量浓度(0、20、40和60 mg/L)硒酸钠的MS培养基上进行培养,35 d后分别测定两种处理材料的过氧化物酶活性、叶绿素、鲜质量和株高等生理生化指标.结果表明:在不同质量浓度硒酸钠处理后,SMT转基因烟草和野生型烟草的叶绿素质量分数、鲜质量及株高均较各自对照明显下降,比较而言,野生型烟草的下降幅度明显大于转基因烟草;另一方面,野生型烟草过氧化物酶(Peroxidase,POD)活性表现强烈的应激反应,其活性明显高于转基因烟草.生长生理与表型特性表明SMT转基因烟草具有一定的硒耐受性. 展开更多
关键词 硒代半胱氨酸甲基转移酶 烟草(Nicotiana tabacum L) 转基因 野生型 叶绿素 过氧化物酶
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茶树ATP硫化酶和硒半胱氨酸甲基转移酶基因植物表达载体的构建 被引量:1
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作者 朱林 江昌俊 +4 位作者 叶爱华 李叶云 余梅 邓威威 房婉萍 《南京农业大学学报》 CAS CSCD 北大核心 2008年第2期121-125,共5页
采用能有效转化双子叶植物的表达载体pBI121构建植物硒营养代谢关键酶基因的表达载体,将原载体中GUS基因用茶树ATP硫化酶基因(APS1和APS2)替换,将硒半胱氨酸甲基转移酶基因(CsSMT)连接到pBI121载体上直接与GUS基因相连,分别构建了目的... 采用能有效转化双子叶植物的表达载体pBI121构建植物硒营养代谢关键酶基因的表达载体,将原载体中GUS基因用茶树ATP硫化酶基因(APS1和APS2)替换,将硒半胱氨酸甲基转移酶基因(CsSMT)连接到pBI121载体上直接与GUS基因相连,分别构建了目的基因植物表达载体pBI-APS1、pBI-APS2和pBI-CsSMT。通过三亲杂交法将重组质粒导入根癌农杆菌LBA4404中,获得转化工程菌,为通过植物基因工程获得富硒农产品打下基础。 展开更多
关键词 茶树 ATP硫化酶 硒半胱氨酸甲基转移酶 基因 植物表达载体
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茶树硒营养代谢关键酶硒半胱氨酸甲基转移酶基因克隆及启动子结构分析 被引量:1
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作者 王雅楠 陈晶晶 朱林 《中国农学通报》 CSCD 2013年第28期138-143,共6页
为探明茶树硒营养代谢关键酶基因硒半胱氨酸甲基转移酶(SMT,GenBank登录号:DQ480337)的表达调控规律,通过PCR和基因步移技术获得SMT的DNA全长和部分启动子序列,用PLACE、PlantCARE分析SMT内含子和启动子的序列,预测其顺式作用元件及功... 为探明茶树硒营养代谢关键酶基因硒半胱氨酸甲基转移酶(SMT,GenBank登录号:DQ480337)的表达调控规律,通过PCR和基因步移技术获得SMT的DNA全长和部分启动子序列,用PLACE、PlantCARE分析SMT内含子和启动子的序列,预测其顺式作用元件及功能。结果表明,SMT基因全长5473 bp,有7个外显子和6个内含子,内含子富含光响应元件、激素响应元件和抗逆性相关元件。通过基因步移法克隆得到的SMT启动子长375 bp,除了含核心启动子保守元件TATA-box和CAAT-box外,还有其他重要顺式作用元件,如光响应元件、低温响应元件和胚乳表达特异性元件等。植物硒营养代谢关键酶SMT启动子的克隆及结构分析为进一步揭示SMT基因的生物学功能和表达调控机制奠定了理论基础。 展开更多
关键词 富硒茶(嫩叶) 硒半胱氨酸甲基转移酶 启动子 基因组步移
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毛薯硒代半胱氨酸甲基转移酶SMT基因的克隆与表达分析 被引量:1
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作者 杨亚飞 黎丹 +3 位作者 黄东益 符晓 夏薇 吴文嫱 《植物遗传资源学报》 CAS CSCD 北大核心 2019年第4期1087-1092,共6页
硒代半胱氨酸甲基转移酶(SMT,Selenocysteine methyltransferase)是植物硒代谢的关键酶,在植物硒积累的过程中发挥着重要作用。为了探究毛薯中SMT基因的功能,本研究以优质富硒毛薯Ds148为研究对象,利用RT-PCR技术从中克隆到了毛薯SMT基... 硒代半胱氨酸甲基转移酶(SMT,Selenocysteine methyltransferase)是植物硒代谢的关键酶,在植物硒积累的过程中发挥着重要作用。为了探究毛薯中SMT基因的功能,本研究以优质富硒毛薯Ds148为研究对象,利用RT-PCR技术从中克隆到了毛薯SMT基因,命名为DsSMT。DsSMT(登录号:MH046782)包含1038 bp完整开放阅读框(ORF),预测编码345个氨基酸,理论分子量(Mw)为37.24 kD,等电点(pI)为5.01,编码的蛋白与其他植物的SMT蛋白同源性较高,具有较高的保守性。系统进化树分析显示,毛薯与海枣和菠萝的SMT蛋白的亲缘关系较近,聚为同一类。利用PSORTⅡ在线软件对DsSMT蛋白进行预测,结果表明其可能定位于细胞质中。实时荧光定量PCR分析显示,DsSMT基因在毛薯生长发育的各个时期的根、茎、叶、块茎以及块茎的皮组织中均有所表达,其中在毛薯的根和成熟期表达量最高。本研究从毛薯中克隆出了硒代谢相关酶DsSMT基因的cDNA序列,并对其进行了生物信息学分析;同时又对DsSMT基因在毛薯块茎形成的不同时期、不同组织中的表达情况进行相对定量的研究和分析,为深入研究DsSMT基因的调控机理提供分子依据,同时也为毛薯硒吸收、同化的分子机理研究奠定基础。 展开更多
关键词 毛薯 硒代半胱氨酸甲基转移酶 基因克隆 生物信息学 表达分析
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鄂马铃薯3号遗传转化体系的构建与表达 被引量:3
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作者 高志鹏 杜玉萧 +3 位作者 冯霞 余土元 李亚男 陈大清 《湖北农业科学》 2022年第9期162-167,191,共7页
以鄂马铃薯(Solanum tuberosum L.)3号为试验材料,将含有来源于黄芪的硒代半胱氨酸甲基转移酶基因(AbSMT)的质粒pBinAr进行PCR扩增以及酶切连接构建重组转化子pBI121-AbSMT,运用农杆菌转化法,设置农杆菌菌液浓度梯度、侵染时间以及共培... 以鄂马铃薯(Solanum tuberosum L.)3号为试验材料,将含有来源于黄芪的硒代半胱氨酸甲基转移酶基因(AbSMT)的质粒pBinAr进行PCR扩增以及酶切连接构建重组转化子pBI121-AbSMT,运用农杆菌转化法,设置农杆菌菌液浓度梯度、侵染时间以及共培养时间组合进行遗传转化,并且通过PCR鉴定以及GUS组织化学染色进行基因表达验证。结果表明,筛选抗生素是50.00 mg/L的Kan,农杆菌菌液浓度为0.50(OD600 nm),侵染时间为8 min,共培养时间为3 d,能够实现鄂马铃薯3号高效遗传转化,同时成功构建了AbSMT基因转化的鄂马铃薯3号。 展开更多
关键词 硒代半胱氨酸甲基转移酶(AbSMT) 马铃薯(Solanum tuberosum L.) 遗传转化 表达分析
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