Photodynamic herbicides. Recent developments and molecular basis of selectivity
- 1 January 1988
- journal article
- research article
- Published by Taylor & Francis in Critical Reviews in Plant Sciences
- Vol. 6 (4) , 385-436
- https://doi.org/10.1080/07352688809382256
Abstract
In 1984, we described the development of a new concept in the design of photodynamic herbicides and demonstrated the phenomenology of the process by using a harmless amino acid, δ‐aminoevulinic acid (see Reference 1 of this article). δ‐Aminolevulinic acid (ALA) is the precursor of all tetrapyrroles in plant and animal cells. By spraying plants with ALA, the latter is converted to tetrapyrroles which accumulate in the plant tissues. In light, the accumulated tetrapyrroles kill some plant species while other plant species are left unharmed. It has recently become apparent that susceptible plant species are divinyl or monovinyl dicotyledonous plants, while monovinyl mono‐cotyledonous plants are less susceptible. At night, monovinyl plant species accumulate mainly monovinyl tetrapyrroles, while divinyl plants accumulate mainly divinyl tetrapyrroles (see Reference 43 of this article). When divinyl plant species are induced to accumulate large amounts of divinyl tetrapyrroles or lesser amounts of monovinyl tetrapyrroles, they are killed by the photodynamic action of the tetrapyrroles in light. Monovinyl plant species appear to evade destruction by conversion of the divinyl tetrapyrroles to monovinyl tetrapyrroles. The latter are then readily converted to chlorophyll in light. Three groups of chemicals which can act in concert with ALA have now been identified, namely: (I) enhancers of ALA conversion to tetrapyrroles, (2) inducers of ALA formation by plant tissues, and (3) inhibitors of divinyl tetrapyrrole conversion to monovinyl tetrapyrroles. By combining ALA with a member(s) of one or more of the foregoing groups of chemicals, it has become possible to design herbicidal formulations which are effective against a wide range of field conditions.Keywords
This publication has 39 references indexed in Scilit:
- Chloroplast Biogenesis 51Plant Physiology, 1985
- Bioengineering of photosynthetic membranes. Requirement of magnesium for the conversion of chlorophyllide a to chlorophyll a during the greening of etiochloroplasts in vitroBiotechnology & Bioengineering, 1984
- Chloroplast biogenesis.42. Conversion of divinyl chlorophyllide a to monovinyl chlorophyllide a in vivo and in vitroPlant Science Letters, 1982
- Chloroplast culture IX chlorophyll(ide) a biosynthesis invitro at rates higher than inMvivoBiochemical and Biophysical Research Communications, 1982
- Magnesium protoporphyrin monoester destruction by extracts of etiolated red kidney bean leavesPlant Science Letters, 1982
- Chloroplast biogenesis. 37. induction of chlorophyllide a (E459 F675) accumulation in higher plantsPlant Science Letters, 1982
- Chloroplast culture VIII a new effect of kinetin in enhancing the synthesis and accumulation of protochlorophyllide invitroBiochemical and Biophysical Research Communications, 1982
- Chloroplast biogenesis: detection of a magnesium protoporphyrin diester pool in plantsBiochemistry, 1981
- Chloroplast biogenesis 30. Chlorophyll(ide) (E459F675) and chlorophyll(ide) (E449F675) the first detectable products of divinyl and monovinyl protochlorophyll photoreductionPlant Science Letters, 1980
- CHLOROPLAST BIOGENESIS. XXIII. THE CONVERSION OF EXOGENOUS PROTOCHLOROPHYLLIDE INTO PHOTOTRANSFORMABLE PROTOCHLOROPHYLLIDE IN VITRO*Photochemistry and Photobiology, 1978