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粘质沙雷氏菌菌株产生的一种诱导型激活剂及其在温室条件下对大豆的促生长活性。

An inducible activator produced by a Serratia proteamaculans strain and its soybean growth-promoting activity under greenhouse conditions.

作者信息

Bai Yuming, Souleimanov Alfred, Smith Donald L

机构信息

Department of Plant Science, Macdonald Campus of McGill University, 21,111 Lakeshore Road, Ste Anne de Bellevue, Quebec, Canada H9X 3V9.

出版信息

J Exp Bot. 2002 Jun;53(373):1495-502.

PMID:12021297
Abstract

Serratia proteamaculans 1-102 (1-102) promotes soybean-bradyrhizobia nodulation and growth, but the mechanism is unknown. After adding isoflavonoid inducers to 1-102 culture, an active peak with a retention time of about 105 min in the HPLC fractionation was isolated using a bioassay based on the stimulation of soybean seed germination. The plant growth-promoting activity of this material was compared with 1-102 culture (cells) and supernatant under greenhouse conditions. The activator was applied to roots in 83, 830 and 8300 HPLC microvolts (microV) per seedling when plants were inoculated with bradyrhizobia or sprayed onto the leaves in same concentrations at 20 d after inoculation. The root-applied activator, especially at 1 ml of 830 microV per seedling, enhanced soybean nodulation and growth at the same level as 1-102 culture under both optimal and sub-optimal root zone temperatures. Thus, this activator stimulating soybean seed germination is also responsible for the plant growth-promoting activity of 1-102 culture. However, when sprayed onto the leaves, the activator did not increase growth and in higher concentrations decreased average single leaf area. The results suggest that this inducible activator might be a lipo-chitooligosaccharide (LCO) analogue. LCOs act as rhizobia-to-legume signals stimulating root nodule formation. The activator could provide additional 'signal', increasing in the signal quality (the signal-to-noise ratio, SNR) of the plant-rhizobia signal exchange process.

摘要

粘质沙雷氏菌1-102(1-102)可促进大豆与慢生根瘤菌的结瘤和生长,但其机制尚不清楚。在向1-102培养物中添加异黄酮诱导剂后,利用基于刺激大豆种子萌发的生物测定法,在高效液相色谱(HPLC)分级分离中分离出一个保留时间约为105分钟的活性峰。在温室条件下,将该物质的促植物生长活性与1-102培养物(细胞)和上清液进行了比较。当用慢生根瘤菌接种植物时,将激活剂以每株幼苗83、830和8300高效液相色谱微伏(μV)的量施用于根部,或在接种后20天以相同浓度喷洒在叶片上。根部施用的激活剂,尤其是每株幼苗1毫升830μV的剂量,在最佳和次最佳根区温度下,与1-102培养物一样增强了大豆的结瘤和生长。因此,这种刺激大豆种子萌发的激活剂也负责1-102培养物的促植物生长活性。然而,当喷洒在叶片上时,激活剂并没有促进生长,且在较高浓度下会降低平均单叶面积。结果表明,这种可诱导的激活剂可能是一种脂壳寡糖(LCO)类似物。LCO作为根瘤菌与豆科植物之间的信号,刺激根瘤形成。该激活剂可以提供额外的“信号”,提高植物-根瘤菌信号交换过程中的信号质量(信噪比,SNR)。

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