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一种基于聚合酶链式反应的技术,用于检测不同高羊茅种质中的内生真菌新麦角菌。

A PCR-Based Technique for Detection of Neotyphodium Endophytes in Diverse Accessions of Tall Fescue.

作者信息

Doss Robert P, Clement Stephen L, Kuy Srey-Reath, Welty Ronald E

机构信息

USDA-ARS, Horticultural Crops Research Unit, Corvallis, OR 97330, and Department of Horticulture, Oregon State University, Corvallis 97331.

USDA-ARS, Western Regional Plant Introduction Station, Pullman, WA 99164.

出版信息

Plant Dis. 1998 Jul;82(7):738-740. doi: 10.1094/PDIS.1998.82.7.738.

Abstract

A previously described polymerase chain reaction (PCR)-based method used for detection of Neotyphodium coenophialum in tall fescue detected Neotyphodium endophytes in some, but not all, infected plants from a geographically diverse sample. In the study reported here, a different set of primers, based on intervening sequences of the tubulin 2 gene, were prepared and used for PCR. PCR with these primers yielded the expected 444 base pair amplification product with DNA from 104 of the 106 infected accessions tested. In addition, one accession originally scored as endophyte-free on the basis of a tissue culture test was correctly rated as endophyte-infected using the PCR procedure. Results suggest that primers based on intervening sequences of the tubulin 2 gene can be used for PCR-based detection of Neotyphodium endophytes in tall fescue accessions of diverse origin.

摘要

一种先前描述的基于聚合酶链反应(PCR)的方法用于检测高羊茅中的内生真菌(Neotyphodium coenophialum),该方法在来自不同地理区域的样本中,能检测出部分而非全部受感染植物中的内生真菌。在本文报道的研究中,基于微管蛋白2基因的间隔序列制备了一组不同的引物,并用于PCR。用这些引物进行PCR时,在所检测的106个受感染材料中,有104个材料的DNA产生了预期的444碱基对扩增产物。此外,一个最初基于组织培养测试被判定为无内生真菌的材料,使用PCR程序被正确地评定为受内生真菌感染。结果表明,基于微管蛋白2基因间隔序列的引物可用于基于PCR的不同来源高羊茅材料中内生真菌的检测。

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