诱导诱变改良保加利亚菜豆(Phaseolus vulgaris L.)产量。

S. Sofkova-Bobcheva, I. Pantchev, I. Kiryakov, P. Chavdarov, Y. Muhovski, F. Sarsu, N. Tomlekova
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引用次数: 1

摘要

虽然历史上是一个过剩的粮食生产国,保加利亚农业在近几十年来面临着低迷。由于与进口品种相比,当地豆类品种的生产率较低,因此已经失去了农民和罐头工业的青睐。疾病和非生物压力是限制食用豆类生产的最重要因素,每年给农民造成数百欧元的收入损失。我们正在进行的大豆突变育种计划的总体目标是丰富菜豆(Phaseolus vulgaris L.)的基因库,并开发抗轴索黄单胞菌(Xanthomonas axonopodis pv)的基因型。phaseoli (Smith) (Xap)和假单胞菌savastanoi pv。用EMS检测phaseolicola (Burkh.) (Psp)。选择保加利亚的一个优良品系和一个普通品种(一个传家宝和一个豆荚型)为亲本,用化学诱变剂EMS进行诱变。总共处理了1000粒种子,产生的两个M1群体在田间种植。所有M2突变株(来自初始品系IP564的1650株和来自初始栽培品种‘Mastilen 11b’的2420株)在大田条件下生长,观察到这些突变株的许多表型变化。并在温室条件下通过叶片人工接种进行了Xap抗病性筛选。对假定具有抗性的M2植株进行了单株选择。M3代采用田间人工接种Xap和Psp病原菌(叶片和荚果)进行筛选。选择抗病的M3-M4系进行鲜荚品质试验。从M4和M5代开始进行产量试验,根据其生产力表现,将突变体提前到M6/M7代进行验证。采用qRT-PCR方法对两种品种的特异基因和内参基因进行了分析。总之,选择了50株具有明显形态变化和/或对两种目标细菌病害的耐受性增强的植物。目前,共有20个高级突变豆系正在多个地点进行竞争力评估。
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Induced mutagenesis for improvement of bean (Phaseolus vulgaris L.) production in Bulgaria.
Abstract Although historically a surplus food producer, Bulgarian agriculture has faced a downturn in recent decades. Local legume cultivars have lost favour with farmers and the canning industry, due to their low productivity in comparison with imported ones. Diseases and abiotic stresses are the most important factors limiting the production of edible legumes, costing farmers hundreds of euros in lost revenue each year. The overall objective of our ongoing bean mutation breeding programme was to enrich the gene pool of Phaseolus vulgaris L. and to develop genotypes resistant to Xanthomonas axonopodis pv. phaseoli (Smith) (Xap) and Pseudomonas savastanoi pv. phaseolicola (Burkh.) (Psp) using EMS. An elite line and common cultivar (an heirloom and a snap bean type) in Bulgaria, were selected as parents and the chemical mutagen EMS was used for generating mutations. In total, 1000 seeds were treated and the two generated M1 populations were grown in the field. All M2 mutant plants (1650 from initial line IP564 and 2420 from initial cultivar 'Mastilen 11b') were grown in field conditions and a number of phenotypic changes were observed on these mutated plants. They were also screened for Xap disease resistance via leaf artificial inoculation under greenhouse conditions. Individual plant selection was performed for the putatively resistant M2 plants. In the M3 generation these lines were screened using artificial inoculation with Xap and Psp pathogens (leaves and pods) under field conditions. Selected M3-M4 lines with confirmed disease resistance were tested for fresh pod quality. Yield tests were started in M4 and M5 generations and, according to their productivity performance, mutants were advanced to the M6/M7 generation for validation. The expression patterns of genes putatively involved in the resistance reactions towards two races of Psp were determined using qRT-PCR for the specific and reference genes. In conclusion, 50 plants with visible morphological changes and/or increased tolerance to the two targeted bacterial diseases were selected. A total of 20 advanced mutant bean lines are currently being evaluated for their competitiveness in multiple sites.
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