Summary
Cell suspension cultures of alfalfa (Medicago sativa L.) accumulated phenolic secondary metabolites in a pattern similar to that seen in alfalfa roots. Upon treatment with a crude elicitor preparation from the bean pathogen Colletotrichum lindemuthianum, the pterocarpan phytoalexin medicarpin accumulated in cells and culture medium. The extractable activities of six enzymes involved in medicarpin biosynthesis (including three cytochrome P450 activities) were induced by treatment with elicitor, and their induction kinetics correlated with the rate of medicarpin accumulation. However, protoplasts prepared from these cultures accumulated neither medicarpin nor other secondary products after treatment with elicitor. The cytochrome P450 activities were induced during the preparation of the protoplasts, but could be further induced by treatment with fungal elicitor. The results are discussed in relation to the use of alfalfa protoplasts as a system for functional analysis of cloned defense genes.
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Abbreviations
- AUFS:
-
absorption unit full scale
- CHI:
-
chalcone isomerase (EC 5.5.1.6)
- CHS:
-
chalcone synthase (EC 2.3.1.74)
- C40H:
-
cinnamic acid 4-hydroxylase (EC 1.14.13.11)
- CLE:
-
elicitor from Colletotrichum lindemuthianum
- IFOH:
-
isoflavone 2′-hydroxylase
- IFS:
-
isoflavone synthase
- PAL:
-
L-phenylalanine ammonia-lyase (EC 4.3.1.5)
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Communicated by A.R. Gould
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Kessmann, H., Choudhary, A.D. & Dixon, R.A. Stress responses in alfalfa (Medicago sativa L.) III. Induction of medicarpin and cytochrome P450 enzyme activities in elicitor-treated cell suspension cultures and protoplasts. Plant Cell Reports 9, 38–41 (1990). https://doi.org/10.1007/BF00232132
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DOI: https://doi.org/10.1007/BF00232132