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Enhancing Biomass Yields- Virtually all high value biochemicals from cultured plant cells are secondary metabolites, which are usually produced in differentiated cells or organised tissues. Therefore, most such biochemicals are not produced by rapidly growing cell cultures, and the culture conditions favouring growth suppress biochemical production (and vice-versa).
Therefore, the production strategy should consist of two distinct phases:
(i) growth phase for cell biomass accumulation and,
(ii) production phase for biosynthesis and accumulation of the biochemicals. But in at least some cases, culture growth and biochemical production occur together, e.g., berberine production in Thalictrum minus.

Biomass accumulation can be improved by using optimum culture conditions of which nutrient medium and inoculum size are particularly important. Experience with L. erythrorhizon cell cultures, which yield shikonin (the first commercial example), suggests the following.

The different standard medium formulations may differ considerably in terms of culture growth; for example, L. erythrorhizon suspension cultures yielded only 6,8 g cell dry weight/l on White's medium, while the yield on LS (Linsmaier and Skoog) medium was 16.8 g/I.

Further improvements in culture growth may be obtained by appropriate modifications of the most suitable standard recipe. A modification of the LS medium (called M-S medium) resulted in a 15% improvement in cell dry weight yields from L. erythrorhizon cultures.
Biomass production can be markedly increased by the use of a larger inoculum size, to give higher initial cell density, in combination with proportionately enriched nutrient medium, e.g., twice the concentration of normal medium for a two-fold increased inoculum size, etc. Often suitable alterations in the medium composition have to be made, and fresh medium may have to be added at regular intervals for optimum biochemical/biomass yields.
In case of C. japonica cell cultures, four-times the normal inoculum (combined with x4 concentration modified medium) yielded 55 g cell dry weight/I as against 14 g/l from normal inoculum combined with normal concentration of the modified medium. However, the berberine yield remained almost constant at 3.5 g/l since the cells from higher inoculum size showed markedly lower berberine content.