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Direct transformation of Neisseria gonorrhoeae by gel-isolated DNA.

作者信息

Pritchard K H, Seifert H S

机构信息

Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, IL 60611, USA.

出版信息

Mol Biotechnol. 1995 Dec;4(3):315-7. doi: 10.1007/BF02779023.

DOI:10.1007/BF02779023
PMID:8680936
Abstract

The naturally competent organism, Neisseria gonorrhoeae, can efficiently transform a marker carried on DNA purified in low-melting-temperature agarose without prior purification or dilution. Neither the agarose or buffer components inhibit transformation frequencies, but exposure to UV irradiation completely abrogates transformation.

摘要

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本文引用的文献

1
NEISSERIA GONORRHOEAE. I. VIRULENCE GENETICALLY LINKED TO CLONAL VARIATION.淋病奈瑟菌。一、与克隆变异基因连锁的毒力。
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Gene. 1993 Jul 15;129(1):51-7. doi: 10.1016/0378-1119(93)90695-y.
3
Identification and arrangement of the DNA sequence recognized in specific transformation of Neisseria gonorrhoeae.
淋病奈瑟菌特异性转化中识别的DNA序列的鉴定与排列
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6982-6. doi: 10.1073/pnas.85.18.6982.
4
Pilin expression in Neisseria gonorrhoeae is under both positive and negative transcriptional control.淋病奈瑟菌中菌毛蛋白的表达受转录正调控和负调控。
EMBO J. 1988 Dec 20;7(13):4367-78. doi: 10.1002/j.1460-2075.1988.tb03335.x.
5
Shuttle mutagenesis of Neisseria gonorrhoeae: pilin null mutations lower DNA transformation competence.淋病奈瑟菌的穿梭诱变:菌毛蛋白缺失突变降低DNA转化能力。
J Bacteriol. 1990 Jan;172(1):40-6. doi: 10.1128/jb.172.1.40-46.1990.
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Cloning, restriction digestion and DNA labeling of large DNA fragments (greater than or equal to 1 kb) in the presence of remelted SeaPlaque GTG agarose gels.在重熔的SeaPlaque GTG琼脂糖凝胶存在下对大DNA片段(大于或等于1 kb)进行克隆、限制性酶切消化和DNA标记。
Biotechniques. 1991 Dec;11(6):784-6, 788, 790-1.