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引用本文的文献

1
A Phytotoxic Glycopeptide from Cultures of Corynebacterium insidiosum.从栖内线菌培养物中分离得到的一种植物毒性糖肽。
Plant Physiol. 1972 May;49(5):676-84. doi: 10.1104/pp.49.5.676.

本文引用的文献

1
Biological Activity of a Phytotoxic Glycopeptide Produced by Corynebacterium sepedonicum.由洋葱伯克霍尔德氏菌产生的具有生物活性的植物毒性糖肽。
Plant Physiol. 1968 Oct;43(10):1673-88. doi: 10.1104/pp.43.10.1673.
2
Purification and Properties of a Phytotoxic Polysaccharide Produced by Corynebacterium sepedonicum.由洋葱伯克霍尔德氏菌产生的一种具有细胞毒性的多糖的纯化和性质。
Plant Physiol. 1967 Oct;42(10):1433-41. doi: 10.1104/pp.42.10.1433.
3
Amino acid metabolism in mammalian cell cultures.哺乳动物细胞培养中的氨基酸代谢
Science. 1959 Aug 21;130(3373):432-7. doi: 10.1126/science.130.3373.432.
4
Studies on the biosynthesis of mannan in Micrococcus lysodeikticus. I. Characterization of mannan-14C formed enzymatically from mannosyl-1-phosphoryl-undecaprenol.溶壁微球菌中甘露聚糖生物合成的研究。I. 由甘露糖基-1-磷酸-十一异戊烯醇酶促形成的14C-甘露聚糖的特性
J Biol Chem. 1969 May 25;244(10):2777-89.
5
A phytotoxic glycopeptide from potato plants infected with Corynebacterium sepedonicum.一种来自感染环腐棒杆菌的马铃薯植株的植物毒性糖肽。
J Biol Chem. 1970 Jan 10;245(1):32-8.
6
The biosynthesis of cell wall lipopolysaccharide in Escherichia coli. 3. The isolation and characterization of 3-deoxyoctulosonic acid.大肠杆菌细胞壁脂多糖的生物合成。3. 3-脱氧辛酮糖酸的分离与特性鉴定。
J Biol Chem. 1966 Jul 10;241(13):3207-15.
7
2-keto-3-deoxygalactonic acid as a constituent of an extra-cellular polysaccharide of Azotobacter vinelandii.2-酮-3-脱氧半乳糖酸作为棕色固氮菌胞外多糖的一种成分
Biochem Biophys Res Commun. 1965 Sep 22;20(6):745-51. doi: 10.1016/0006-291x(65)90080-x.

马铃薯环腐棒杆菌植物毒素的活性位点

The Active Site on the Phytotoxin of Corynebacterium sepedonicum.

作者信息

Johnson T B, Strobel G A

机构信息

Department of Botany and Microbiology, Montana State University, Bozeman, Montana 59715.

出版信息

Plant Physiol. 1970 Jun;45(6):761-4. doi: 10.1104/pp.45.6.761.

DOI:10.1104/pp.45.6.761
PMID:16657388
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC396508/
Abstract

Corynebacterium sepedonicum produces an extracellular phytotoxic glycopeptide that possesses a capacity to wilt plant cuttings. It has been previously demonstrated that the integrity of some of the membranes of the host cells is destroyed, suggesting the possibility that a biologically active site is present on the toxin molecule. The toxin was chemically altered in the following ways and then tested for biological activity: (a) the NH(2)-terminal group on the peptide portion of the toxin was blocked by the dansylation technique; (b) the OH groups on the sugar and amino acid residues as well as the NH groups on the amino acid residues were blocked by exhaustive methylation; (c) the COO(-) groups were converted to their respective methyl esters; (d) the peptide moiety was removed by pronase digestion. Experimental results indicate that the carboxyl groups of the nonpeptide portion of the molecule are responsible for the biological activity of the toxin. Other experiments showed that the toxin does not affect the membranes of animal cells.The biological activity of the glycopeptide, as well as its chemically altered derivatives, was determined by an instrument designated as a wilt-o-meter that quantitatively measures the strength of plant cuttings. A description of this instrument, how it is used, and how it can be manufactured is also included in this report.

摘要

马铃薯环腐棒杆菌产生一种细胞外植物毒性糖肽,它具有使植物插条枯萎的能力。先前已经证明宿主细胞的一些膜的完整性被破坏,这表明毒素分子上可能存在生物活性位点。毒素通过以下方式进行化学改变,然后测试其生物活性:(a)毒素肽部分的NH(2)-末端基团通过丹磺酰化技术被封闭;(b)糖和氨基酸残基上的OH基团以及氨基酸残基上的NH基团通过彻底甲基化被封闭;(c)COO(-)基团被转化为它们各自的甲酯;(d)肽部分通过链霉蛋白酶消化被去除。实验结果表明,分子非肽部分的羧基负责毒素的生物活性。其他实验表明,该毒素不影响动物细胞的膜。糖肽及其化学改变的衍生物的生物活性通过一种称为枯萎测量仪的仪器来测定,该仪器定量测量植物插条的强度。本报告还包括该仪器的描述、其使用方法以及如何制造。