Del Giudice L, Massardo D R, Manna F, Wolf K
Istituto Internazionale di Genetica e Biofisica, Consiglio Nazionale delle Ricerche, Napoli, Italia.
Curr Genet. 1986;11(3):247-9. doi: 10.1007/BF00420614.
Mutants resistant to 200 micrograms/ml of the alkaloid lycorine (LYCR) in non-fermentable substrate were isolated after nitrosoguanidine mutagenesis. Tetrad analysis and growth of heterozygous (LYCR/lycS) diploids from two different mutants revealed that a single nuclear and dominant mutation is responsible for the resistant phenotype. In the wild type total protein synthesis is only slightly inhibited, whereas DNA and RNA synthesis is lowered to about 30% of the control. In the lycorine resistant mutants all macromolecular syntheses are unaffected by the drug.
在用亚硝基胍诱变后,从不可发酵底物中分离出对200微克/毫升生物碱石蒜碱(LYCR)具有抗性的突变体。对来自两个不同突变体的杂合子(LYCR/lycS)二倍体进行四分体分析和生长研究表明,单个核显性突变导致了抗性表型。在野生型中,总蛋白质合成仅受到轻微抑制,而DNA和RNA合成降至对照的约30%。在石蒜碱抗性突变体中,所有大分子合成均不受该药物影响。