首页> 外文期刊>Molecular and Cellular Biology >Molecular cloning of a Neurospora crassa carotenoid biosynthetic gene (albino-3) regulated by blue light and the products of the white collar genes.
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Molecular cloning of a Neurospora crassa carotenoid biosynthetic gene (albino-3) regulated by blue light and the products of the white collar genes.

机译:蓝光和白领基因产物调控的神经孢霉类胡萝卜素生物合成基因(albino-3)的分子克隆。

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The albino-3 (al-3) gene of Neurospora crassa, which probably encodes the carotenoid biosynthetic enzyme geranylgeranyl pyrophosphate synthetase, was cloned. The N. crassa triple mutant al-3 qa-2 aro-9 was transformed to qa-2+ with mixtures of plasmids bearing N. crassa DNA inserts, and the transformants were screened for the al-3+ phenotype. One al-3+ qa-2+ transformant (AL3-1) was examined in detail and shown to contain intact vector sequences integrated into the N. crassa genome. The vector and some flanking sequences were recovered from AL3-1 after restriction, ligation, and selection of chloramphenicol-resistant transformants of Escherichia coli. The flanking sequences were subsequently used to detect the al-3-containing plasmid in the mixture of about 1,800 plasmids. Restriction fragment length polymorphism mapping was carried out to confirm the identity of the cloned fragment. The level of the al-3 mRNA was shown to be increased 15-fold in light-induced (compared with that in dark-grown) wild-type mycelia. The light-dependent increase in al-3 mRNA levels was not observed in presumed regulatory mutant (white collar) strains.
机译:克隆了可能存在的类胡萝卜素生物合成酶Geranylgeranyl焦磷酸合成酶的Neurospora crassa的albino-3(al-3)基因。用带有N.crassa DNA插入片段的质粒混合物将N. crassa三重突变体al-3 qa-2 aro-9转化为qa-2 +,并筛选转化子的al-3 +表型。详细检查了一种al-3 + qa-2 +转化子(AL3-1),显示其包含整合到crassa烟草基因组中的完整载体序列。在限制,连接和选择大肠杆菌的抗氯霉素的转化子后,从AL3-1中回收了载体和一些侧翼序列。随后将侧翼序列用于检测约1,800个质粒的混合物中的含al-3的质粒。进行限制性片段长度多态性作图以确认克隆片段的身份。在光诱导的野生型菌丝体中,与光暗诱导的相比,al-3 mRNA的水平提高了15倍。在推测的调节突变体(白领)菌株中未观察到al-3 mRNA水平的光依赖性增加。

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