natural-products-in-plant-pest-management
natural-products-in-plant-pest-management
natural-products-in-plant-pest-management
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272 S. Hettiarachi1980), cont<strong>in</strong>uous efforts have been made experiment<strong>in</strong>g with various cellsuspension culture techniques with modifications of culture conditions <strong>in</strong>order to maximize the production of desired compounds. The research focus<strong>in</strong>gon improvements on both cell culture and bioreactor aspects is the subjectof the review by Zhao and Verpoorte (2007). Nevertheless, further research isnecessary to br<strong>in</strong>g <strong>products</strong> of C. roseus to the commercial scale. Berber<strong>in</strong>e, anisoqu<strong>in</strong>olene alkaloid, has been produced <strong>in</strong> cell suspension culture of T<strong>in</strong>osporacordifolia at a concentration of 5.5 mg g −1 dry wt <strong>in</strong> 24 days (Rao et al.,2008). By screen<strong>in</strong>g eight cell l<strong>in</strong>es, the authors were able to f<strong>in</strong>d one l<strong>in</strong>e thataccumulated 13.9 mg g −1 dry weight of berber<strong>in</strong>e. This is a 5–14-fold <strong>in</strong>crease<strong>in</strong> product formation compared to that of the <strong>in</strong>tact <strong>plant</strong>. This is an exampledemonstrat<strong>in</strong>g the potential of <strong>plant</strong> cell cultures and somaclonal variationfor the <strong>natural</strong> product <strong>in</strong>dustry. A tenfold <strong>in</strong>crease br<strong>in</strong>gs down the cost ofthe product <strong>in</strong> the market by at least the same magnitude.Cyclotides are small cyclic peptides stabilized by disulfide bonds betweensix conserved cyst<strong>in</strong>e residues. Their biological activities <strong>in</strong>clude anti-HIV,antimicrobial and <strong>in</strong>secticidal actions, and hence they are important botanicals<strong>in</strong> biocontrol. In addition, due to their high stability, cyclo tides are verygood candidates for the development of drug delivery systems. Dörnenburget al. (2008) developed techniques to produce cyclotides us<strong>in</strong>g callus, suspensionculture and hydroponic cultures of Oldenlandia aff<strong>in</strong>is and evaluated themfor Kalata B1 accumulation. In vitro culture produced only up to 15% of KalataB1 <strong>in</strong> comparison with <strong>plant</strong>s grown <strong>in</strong> hydroponics. Further improvement isprobable by manipulat<strong>in</strong>g culture conditions and the same group reported ahigher rate of cell multiplication <strong>in</strong> a 25-l photobioreactor (Seydel et al., 2009).They claim that this approach for harvest<strong>in</strong>g Kalata B1 is more profitable thanother methods, such as field cultivation and chemical synthesis.Cell suspension culture is also useful <strong>in</strong> the synthesis of volatile oils. Bymanipulat<strong>in</strong>g culture conditions, Ishikura et al. (1984) obta<strong>in</strong>ed a yield of0.005% to 0.01% of volatile oils of the fresh weight of the cells of Cryptomeriajaponica cell suspension.The progress of research <strong>in</strong> the development of hairy root technology formetabolite production has been reviewed by Guillon et al. <strong>in</strong> 2006. The delicatenature of the hairy roots is one of the major problems <strong>in</strong> ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>ghairy root cultures. Srivastava and Srivastava (2007) reviewed the problemsand different technologies available to overcome them. The basic types ofreactors are either liquid phase or gas phase or even a comb<strong>in</strong>ation of the two.The nature, applications, perspectives and scale up are discussed there<strong>in</strong>.The hairy root growth, production of the desired substance(s) and secretionmay require different culture conditions. The production can be enhancedby provid<strong>in</strong>g the precursors at the right time and the right concentration. Theaddition of cadaver<strong>in</strong>e to hairy root cultures of Nicotiana rustica shifted thealkaloid production <strong>in</strong> considerable favour of anabas<strong>in</strong>e with a concomitantdim<strong>in</strong>ution of nicot<strong>in</strong>e (Walton et al., 1988), whereas the addition of mentholor geraniol at 25 mg l −1 to hairy root cultures of Anethum graveolens did nothave an impact on the growth and resulted <strong>in</strong> the transformation of thecompounds to volatile <strong>products</strong> (Faria et al., 2009). In a recent experiment,