Sannazzaro Analía I, Alvarez Cora L, Menéndez Ana B, Pieckenstain Fernando L, Albertó Edgardo O, Ruiz Oscar A
Instituto de Investigaciones Biotecnológicas, Universidad Nacional de General San Martín, Consejo Nacional de Investigaciones Científicas y Técnicas, Chascomús, Buenos Aires, Argentina.
FEMS Microbiol Lett. 2004 Jan 15;230(1):115-21. doi: 10.1016/S0378-1097(03)00880-2.
The pathways for putrescine biosynthesis and the effects of polyamine biosynthesis inhibitors on the germination and hyphal development of Gigaspora rosea spores were investigated. Incubation of spores with different radioactive substrates demonstrated that both arginine and ornithine decarboxylase pathways participate in putrescine biosynthesis in G. rosea. Spermidine and spermine were the most abundant polyamines in this fungus. The putrescine biosynthesis inhibitors alpha-difluoromethylarginine and alpha-difluoromethylornithine, as well as the spermidine synthase inhibitor cyclohexylamine, slightly decreased polyamine levels. However, only the latter interfered with spore germination. The consequences of the use of putrescine biosynthesis inhibitors for the control of plant pathogenic fungi on the viability of G. rosea spores in soil are discussed.
研究了腐胺生物合成途径以及多胺生物合成抑制剂对玫瑰巨孢囊霉孢子萌发和菌丝发育的影响。用不同放射性底物培养孢子表明,精氨酸脱羧酶途径和鸟氨酸脱羧酶途径均参与玫瑰巨孢囊霉中腐胺的生物合成。亚精胺和精胺是该真菌中含量最丰富的多胺。腐胺生物合成抑制剂α-二氟甲基精氨酸和α-二氟甲基鸟氨酸以及亚精胺合酶抑制剂环己胺可使多胺水平略有降低。然而,只有后者会干扰孢子萌发。讨论了使用腐胺生物合成抑制剂控制植物病原真菌对土壤中玫瑰巨孢囊霉孢子活力的影响。