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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >QUANTITATIVE MEASUREMENT OF THE ABILITY OF DIFFERENT MUTAGENS TO INDUCE AN INHERITED CHANGE IN PHENOTYPE TO ALLOW MALTOSE UTILIZATION IN SUSPENSION CULTURES OF THE SOYBEAN, GLYCINE MAX (L.) MERR
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QUANTITATIVE MEASUREMENT OF THE ABILITY OF DIFFERENT MUTAGENS TO INDUCE AN INHERITED CHANGE IN PHENOTYPE TO ALLOW MALTOSE UTILIZATION IN SUSPENSION CULTURES OF THE SOYBEAN, GLYCINE MAX (L.) MERR

机译:定量测定不同诱变剂诱导表型的遗传变化以允许大豆悬浮培养物中麦芽糖利用的最大量

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Using a newly developed plating system, we have measured cell survival and the frequencies of variation in an inherited trait after treatment of soybean cell suspensions with different mutagens: ethyl methanesulfonate (EMS), methyl methanesulfonate (MMS), N-Methyl-N′-nitro-N-nitroso-guanidine (MNNG), hycanthone (1-{[2-(diethylamino) ethyl] amino}-4-(hydroxymethyl)-9H-thioxanthen-9-one and ultraviolet light (UV).—The heritable variation selected for displays a phenotype of rapid growth on maltose as carbon source. The marker is stable in the absence of maltose, and prolonged growth of variant cells on sucrose has not shown reversions to slow growth. Doubling time in suspension cultures is decreased from 100 hr to ca . 30 hr by the mutation. Both wild-type and variant cells grow on sucrose with a 24-hr doubling time. Thus, lethality after mutagen treatment can be estimated rapidly by growth on sucrose, whereas variants are scored on maltose medium. The spontaneous frequency of variants was 1.2 × 10-7; induced frequencies ranged from a low of 3.6 × 10-5 for EMS to a high of 10-3 for hycanthone. The high frequency of variants induced by hycanthone, a frame-shift mutagen, and the observation that UV induces variants in haploid cells with much higher frequency than in diploid cells suggests a recessive mutation.
机译:使用新开发的平板系统,我们测量了不同诱变剂处理的大豆细胞悬液后的细胞存活率和遗传性状的变异频率:不同的诱变剂:甲烷磺酸乙酯(EMS),甲烷磺酸甲酯(MMS),N-甲基-N'-硝基-N-亚硝基胍(MNNG),庚酮(1-{[2-(二乙氨基)乙基]氨基} -4-(羟甲基)-9H-噻吨酮-9-和紫外线(UV)。所选择的变异体在麦芽糖作为碳源时表现出快速生长的表型。在没有麦芽糖的情况下该标记物是稳定的,并且蔗糖上的变异细胞的长期生长没有显示出恢复到缓慢的生长。悬浮培养的倍增时间从100突变大约需要30到30个小时,野生型和变异型细胞都可以在蔗糖上生长,且倍增时间为24小时,因此,诱变剂处理后的致死性可以通过蔗糖上的生长来快速估算,而变异型则在麦芽糖培养基上评分。变体w的自发频率为1.2×10-7;感应频率范围从EMS的3.6×10-5的低点到Hycanthone的10-3的高点。由庚酮,移码诱变剂诱导的变异体的高频率,以及观察到紫外线在单倍体细胞中诱导变异体的频率远高于二倍体细胞,这表明是隐性突变。

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