Journal of Plant Biochemistry and Biotechnology
  • Year: 1995
  • Volume: 4
  • Issue: 2

In Vitro Flowering and High Xanthotoxin in Ammi majus L.

  • Author:
  • Madhumati Purohit, Deepshikha Pande, Aniruddha Datta, Prem S Srivastava
  • Total Page Count: 4
  • Page Number: 73 to 76

Tissue Culture Laboratory, Department of Botany, Faculty of Science, Hamdard University, Hamdard Nagar, New Delhi 110 062, India

* Corresponding author.

AbbreviationsMS

Murashige and Skoog's medium

IAA

Indole acetic acid

Kn

Kinetin

CH

Casein hydrolysate

IBA

lndolebutyric acid

BAP

6-Benzylaminopurine

LAP

Leucineaminopeptidase

TLC

Thin layer chromatography

HPLC

High performance liquid chromatography

Abstract

Ammi majus L. (Apiaceae), an important medicinal herb, constitutes the principal commercial source of xanthotoxin that is commonly used in leucoderma. Since the seed set and germination is poor, the present investigation was undertaken to propagate A. majus through tissue culture and monitor the yield of xanthotoxin (f uranocoumarin) in the resultant callus and plantlets. The callus obtained from the cotyledonary leaves on MS medium supplemented with indoleacetic acid (IAA) + kinetin (Kn) + casein hydrolysate (CH), differentiated shoot buds on a medium additionally enriched with adenine. Plantlets 3.5 cm tall, resulted upon transfer of shoots to MS medium with indolebutyric acid (IBA) and glutamine. These plantlets flowered in vitro The yield of xanthotoxin detected in regenerating cultures is more than hitherto reported from any other tissue including the seeds. Isozymes profile for leucineaminopeptidase (LAP), esterase and peroxidase could be used as reliable markers for the characterization of various stages of growth of callus and regenerants. The present report would prove advantageous in multiplication of Ammi majus and also in inducing enhanced levels of xanthotoxin.

Keywords

Ammi majus, Bishop's weed, tissue culture, regeneration, xanthotoxin