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2
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本文引用的文献

1
Trifolitoxin Production and Nodulation Are Necessary for the Expression of Superior Nodulation Competitiveness by Rhizobium leguminosarum bv. trifolii Strain T24 on Clover.三叶草诺卡氏菌 T24 菌株在三叶草上表现出优异结瘤竞争能力需要三叶草诺卡氏菌素的产生和结瘤。
Plant Physiol. 1987 Oct;85(2):335-42. doi: 10.1104/pp.85.2.335.
2
Growth Factor Requirements of the Root Nodule Bacteria.根瘤菌的生长因子需求
J Bacteriol. 1939 Feb;37(2):161-85. doi: 10.1128/jb.37.2.161-185.1939.
3
Greenhouse and Field Evaluations of an Autoselective System Based on an Essential Thymidylate Synthase Gene for Improved Maintenance of Plasmid Vectors in Modified Rhizobium meliloti.温室和田间评价基于必需胸苷酸合酶基因的自动选择系统,以改进改良苜蓿根瘤菌中质粒载体的维持。
Appl Environ Microbiol. 1995 Nov;61(11):4051-6. doi: 10.1128/aem.61.11.4051-4056.1995.
4
Improvement of Rhizobium inoculants.根瘤菌接种剂的改良。
Appl Environ Microbiol. 1989 Apr;55(4):862-5. doi: 10.1128/aem.55.4.862-865.1989.
5
Biotin and other water-soluble vitamins are key growth factors for alfalfa root colonization by Rhizobium meliloti 1021.生物素和其他水溶性维生素是苜蓿中华根瘤菌1021在苜蓿根部定殖的关键生长因子。
Mol Plant Microbe Interact. 1996 Jul;9(5):330-8. doi: 10.1094/mpmi-9-0330.
6
Evaluation of a strategy for identifying nodulation competitiveness genes in Rhizobium leguminosarum biovar phaseoli.评估一种鉴定菜豆根瘤菌生物变种中结瘤竞争基因的策略。
J Gen Microbiol. 1993 Mar;139(3):529-38. doi: 10.1099/00221287-139-3-529.
7
Molecular breeding of a biotin-hyperproducing Serratia marcescens strain.一株生物素高产粘质沙雷氏菌菌株的分子育种
Appl Environ Microbiol. 1993 Oct;59(10):3225-32. doi: 10.1128/aem.59.10.3225-3232.1993.
8
Alfalfa yield response to inoculation with recombinant strains of Rhizobium meliloti with an extra copy of dctABD and/or modified nifA expression.紫花苜蓿对接种带有额外一份dctABD拷贝和/或修饰的nifA表达的重组苜蓿根瘤菌菌株的产量响应。
Appl Environ Microbiol. 1994 Oct;60(10):3815-32. doi: 10.1128/aem.60.10.3815-3832.1994.
9
Molecular analysis of growth inhibition caused by overexpression of the biotin operon in Escherichia coli.大肠杆菌中生物素操纵子过表达导致生长抑制的分子分析。
Biosci Biotechnol Biochem. 1995 Feb;59(2):184-9. doi: 10.1271/bbb.59.184.
10
Determination of biotin concentration by a competitive enzyme-linked immunosorbent assay (ELISA) method.采用竞争性酶联免疫吸附测定(ELISA)法测定生物素浓度。
J Biochem Biophys Methods. 1994 Dec;29(3-4):321-9. doi: 10.1016/0165-022x(94)90042-6.

具有额外生物素合成能力的重组苜蓿根瘤菌菌株。

Recombinant Rhizobium meliloti strains with extra biotin synthesis capability.

作者信息

Streit W R, Phillips D A

机构信息

Department of Agronomy and Range Science, University of California, Davis 95616, USA.

出版信息

Appl Environ Microbiol. 1996 Sep;62(9):3333-8. doi: 10.1128/aem.62.9.3333-3338.1996.

DOI:10.1128/aem.62.9.3333-3338.1996
PMID:8795223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC168129/
Abstract

The growth of Rhizobium meliloti 1021 in an experimental alfalfa (Medicago sativa L.) rhizosphere was stimulated by adding nanomolar amounts of biotin. To overcome this biotin limitation, R. meliloti strains were constructed by conjugating the Escherichia coli biotin synthesis operon into biotin auxotroph R. meliloti 1021-B3. Transconjugant strains Rm1021-WS10 and Rm1021-WS11 grew faster in vitro and achieved a higher cell density than did R. meliloti 1021 and overproduced biotin on a defined medium. The increase in cell yield was associated with as much as a 99% loss in viability for Rm1021-WS11, but data suggested that a separate stabilizing factor in the E. coli DNA reduced cell death in Rm1021-WS10. In rhizosphere tests, the recombinant strains showed delayed growth and competed poorly against Rm1021.

摘要

添加纳摩尔量的生物素可刺激苜蓿中华根瘤菌1021在实验性苜蓿(紫花苜蓿)根际的生长。为克服这种生物素限制,通过将大肠杆菌生物素合成操纵子与生物素营养缺陷型苜蓿中华根瘤菌1021 - B3进行接合,构建了苜蓿中华根瘤菌菌株。转接合子菌株Rm1021 - WS10和Rm1021 - WS11在体外生长更快,细胞密度高于苜蓿中华根瘤菌1021,并且在限定培养基上生物素过量产生。细胞产量的增加与Rm1021 - WS11高达99%的活力丧失有关,但数据表明大肠杆菌DNA中的一个单独稳定因子减少了Rm1021 - WS10中的细胞死亡。在根际试验中,重组菌株生长延迟,与Rm1021竞争能力差。