Considerable progress has been made during the past two decades on the development of media for growing plant cells, tissues and organs aseptically in culture. A significant contribution to formulation of a defined growth medium suitable for a wide range of applications was made by Murashige and Skoog (1962), In their work to adapt tobacco callus cultures for use as a hormone bioassay system, they evaluated many medium constituents to achieve optimal growth of calluses. In so doing, they improved upon existing types of plant tissue culture media to such an extent that their medium (the MS medium) has since proved to be one of the most widely used in plant tissue culture work gives the composition of different media.
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