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Cain can gain

Dr Vibha Dhawan emphasises that the tissue culture of new varieties and multiplication of the existing disease free varieties might help in improving per unit productivity of cane.

Dr Vibha Dhawan

In this era of globalisation, farmers in the developing countries with smallholdings and meagre resources have a challenging task of competing in the international markets. While globalisation has offered tremendous opportunities – whereby a farmer is free to sell his produce not just in the domestic markets but world over – it has also posed threats, which cannot be ignored.

The customer today wants quality produce at a competitive price. Thus, the marginal farmers in a developing country have the daunting task of producing quality product as well as compete with large farmers in industrialised countries, who apart from utilising technologically advanced seeds, equipment, irrigation facilities and fertilisers also enjoy farm subsidies.

Being an agri-based economy, where agriculture contributes over 35 per cent to the GDP and provides a livelihood to over 65 per cent of the population, the task before us is to supplement ongoing efforts with newer biotechnological tools to increase productivity.

INTRICACIES OF MICROPROPAGATION

Micropropagation is a technique of producing millions of identical plants from a millimetre or centimetre long explants collected from an elite plant or seed. The general techniques of micropropagation involves the following stages:

  • Selection and preparation of mother plant m Initiation of aseptic culture
  • Shoot multiplication
  • Shoot elongation m Rooting of in-vitro formed shoots
  • Transplantation to potting mix.

Each stage has its own special requirements specific to individual species. Also, all species may not require to be treated for all the stages.

It is of utmost importance to identify the mother plants carefully as micropropagation techniques do not bring any improvement in the genetic make-up of the plant and only produce mirror images of the selected mother plant.

Further, as the plants grow in the field, they are exposed to a large number of microbial contaminants and thus harbour a large number of micro-organisms on their surface and sometimes also have a high level of endogenous bacteria, yeast-like microorganisms, fungi, and virus.

In these instances, the mother plants are prepared for raising aseptic cultures and various techniques for rejuvenating the material such as pollarding and coppicing are attempted.

Growing cuttings in the green house or covering them with poly-bags or spraying them with fungicides are some other parameters used for preparing mother plants for raising aseptic cultures. Explants are then sterilised to ensure removal of microbial contamination by treating with chemicals and then put on the sterilised growth medium.

The growth medium typically contains the energy source, major and minor salts, vitamins and growth regulators required to stimulate growth in the explant.

The most common method of shoot multiplication for cloning is through the enhanced axillary method. The axillary bud found in the axil of each leaf has the potential to develop into a shoot. In normal conditions these buds remain dormant but if the terminal bud is injured, the next axillary sprout takes over the role of the terminal bud. This phenomenon is controlled by the interplay of growth regulators.

The excised nodal explants, thus, when provided with appropriate conditions for the growth of the shoot, show sprouting of axillary buds. Depending on the species, it can be either a single shoot or a cluster of shoots, which can be separated every three weeks for further multiplication. Once enough shoots are formed, they are put for rooting.

Although plants propagated through tissue culture appear to be green in colour, they are neither capable of efficient photosynthesis nor are they equipped with a proper mechanism to control

 

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