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Phytotoxic and Photosynthetic Activities of Maduramicin and Maduramicin Methyl Ester

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Phytotoxic and Photosynthetic Activities of Maduramicin and Maduramicin Methyl Ester

Maria Teresa Gutie´rrez-Lugo

a

, Blas Lotina-Hennsen

b

, Amelia Farre´s

c

, Sergio Sa´nchez

d

and Rachel Mata

a

a Departamento de Farmacia, Facultad de Quı´mica, Universidad Nacional Auto´noma de Me´xico, Coyoaca´n 04510, Me´xico, D. F., Me´xico

b Departamento de Bioquı´mica, Facultad de Quı´mica, Universidad Nacional Auto´noma de Me´xico, Coyoaca´n 04510, Me´xico, D. F., Me´xico

c Departamento de Biotecnologı´a, Facultad de Quı´mica, Universidad Nacional Auto´noma de Me´xico, Coyoaca´n 04510, Me´xico, D. F., Me´xico

d Departamento de Biotecnologı´a, Instituto de Investigaciones Biome´dicas, Universidad Nacional Auto´noma de Me´xico, Coyoaca´n 04510, Me´xico, D. F., Me´xico

Z. Naturforsch.54 c,325Ð332 (1999); received October 21/December 23, 1998 Maduramicin, Photophosphorylation, Uncoupler, Phytotoxicity, Polyether Antibiotic

The polyether antibiotic maduramicin and its methyl ester derivative inhibited photophos- phorylation and proton uptake in isolated spinach chloroplasts. Both compounds also en- hanced basal and phosphorylating electron transport and stimulated Mg2+-dependent AT- Pase activity, therefore, they behave as uncouplers of photophosphorylation being the methyl ester derivative more potent than the parent compound. On the other hand, maduramicin inhibited germination and radicle elongation of several cropand weed species. In addition, the antibiotic caused phytotoxic injury and fresh weight reduction to 4-to-6 week old seed- lings of two weed and two crop species when applied at 10Ð4 m by foliar application in the greenhouse.

Reprint requests to Dr. Lotina-Hennsen or Dr. Rachel Mata. Fax: (525) 6225329.

E-mail: blas@servidor.unam.mx, rachel@servidor.unam.mx

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