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L-(−)-Malic acid

L - ( - ) - 苹果酸

Company: Sigma-Aldrich
Catalog#: M1000
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Electro-fusion of Gametes and Subsequent Culture of Zygotes in Rice
Author:
Date:
2016-12-20
[Abstract]  Electro-fusion system with isolated gametes has been utilized to dissect fertilization-induced events in angiosperms, such as egg activation, zygote development and early embryogenesis, since the female gametophytes of plants are deeply embedded within ovaries. In this protocol, procedures for isolation of rice gametes, electro-fusion of gametes, and culture of the produced zygotes are described. [摘要]  已经利用具有孤立配子的电融合系统来解剖被子植物中受精诱导的事件,例如卵活化,合子发育和早期胚胎发生,因为植物的雌配子体深深嵌入卵巢内。在该方案中,描述了分离水稻配子,配子电融合和产生的受精卵培养的程序。

背景 被子植物的受精和后续事件,如胚胎发生和胚乳发育,发生在深入嵌入卵母细胞的胚囊中(Nawaschin,1898; Guignard,1899; Russell,1992; Raghavan,2003)。因此,分离的配子已被用于体外受精(IVF)系统,以观察和分析受精和后处理过程(Wang等人,2006年)。用于被子植物的IVF系统包括三种基本微技术的组合:(i)男性和女性配子的分离和选择; (ii)配对对和(iii)单细胞培养物的融合(Kranz,1999)。已经在广泛的植物物种中建立了分离活的配子的程序,包括单子叶植物和双子叶植物(综述于Kranz,1999和Okamoto,2011)。分离的配子可以电融合(Kranz等人,1991; Uchiumi等人,2006和2007)或化学地使用钙(Faure等人,1994; Kranz和Lörz,1994; Khalequzzaman和Haq,2005),聚乙二醇(Sun等,1995; ...

Extraction and Measurement the Activities of Cytosolic Phosphoenolpyruvate Carboxykinase (PEPCK) and Plastidic NADP-dependent Malic Enzyme (ME) on Tomato (Solanum lycopersicum)
Author:
Date:
2014-05-05
[Abstract]  A recent study demonstrated that cytosolic phosphoenolpyruvate carboxykinase (PEPCK) and NADP-malic enzyme (NADP-ME) have an important role in malate metabolism during fruit ripening (Osorio et al., 2013). PEPCK catalyze the ATP-dependent decarboxylation of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) and NADP-ME, the reversible conversion of malate and pyruvate. Here, we present the detailed protocols to measure PEPCK activity in carboxylation direction by following oxidation of NADH and to measure NADP-ME activity based upon the reduction of NADP+. [摘要]  最近的研究表明胞质磷酸烯醇丙酮酸羧激酶(PEPCK)和NADP-苹果酸酶(NADP-ME)在果实成熟期间在苹果酸代谢中具有重要作用(Osorio等人,2013)。 PEPCK催化草酰乙酸(OAA)向磷酸烯醇丙酮酸(PEP)和NADP-ME的ATP依赖性脱羧,苹果酸和丙酮酸的可逆转化。 在这里,我们提出详细的协议,以测量PEPCK活性的羧化方向通过以下氧化NADH和基于NADP + 的还原测量NADP-ME活性。

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