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在对厌氧真菌新美鞭菌进行生物弹道转化后β-葡萄糖醛酸酶基因的瞬时表达

Transient expression of the beta-glucuronidase gene after biolistic transformation of the anaerobic fungus Neocallimastix frontalis.

作者信息

Durand R, Rascle C, Fischer M, Fèvre M

机构信息

Laboratoire de Biologie Cellulaire Fongique, Centre de Génétique Moléculaire et Cellulaire, CNRS UMR 5534, Bât 405, Université Claude Bernard Lyon I, F-69622 Villeurbanne Cedex, France.

出版信息

Curr Genet. 1997 Feb;31(2):158-61. doi: 10.1007/s002940050190.

Abstract

The rumen anaerobic fungus Neocallimastix frontalis was biolistically transformed using plasmids containing the bacterial beta-glucuronidase gene (GUS) fused to the promoter sequences of the enolase gene from N. frontalis. Multiple copies of the plasmids were precipitated onto tungsten particles and delivered into zoosporangia and a mycelial mat by a helium-driven biolistic device. Transformants were detected by histochemical assay for beta-glucuronidase. It was found that the enolase promoter sequences tested were responsible for the transient expression of the beta-glucuronidase gene. This is the first study presenting results on the transformation of an anaerobic fungus.

摘要

利用含有与来自额叶新丽鞭毛虫(Neocallimastix frontalis)的烯醇酶基因启动子序列融合的细菌β-葡萄糖醛酸酶基因(GUS)的质粒,对瘤胃厌氧真菌额叶新丽鞭毛虫进行了生物弹射击转化。将多个质粒拷贝沉淀到钨颗粒上,并通过氦驱动的生物弹射击装置将其导入游动孢子囊和菌丝体垫中。通过β-葡萄糖醛酸酶的组织化学测定来检测转化体。结果发现,所测试的烯醇酶启动子序列负责β-葡萄糖醛酸酶基因的瞬时表达。这是第一项展示厌氧真菌转化结果的研究。

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