By Michael Wink
This fresh Annual Plant experiences quantity is the second one variation of the hugely winning and well-received Annual Plant experiences, quantity 2.
This fascinating new quantity presents an updated survey of the biochemistry and body structure of plant secondary metabolism. the quantity commences with an summary of the biochemistry, body structure and serve as of secondary metabolism, via certain stories of the key teams of secondary metabolites: alkaloids and betalains, cyanogenic glucosides, glucosinolates and nonprotein amino acids, phenyl propanoids and similar phenolics, terpenoids, cardiac glycosides and saponins. a last bankruptcy discusses the evolution of secondary metabolism.
This conscientiously compiled new version brings jointly chapters from a few of the world's top specialists in plant secondary metabolism. thoroughly revised and taken correct brand new with a lot new info, this quantity is an important buy for complicated scholars, researchers and pros in biochemistry, body structure, molecular biology, genetics, plant sciences, agriculture, medication, pharmacology and pharmacy, operating within the educational and commercial sectors, together with these operating within the pesticide and pharmaceutical industries. Libraries in all universities and examine institutions the place those topics are studied and taught will desire copies of this wonderful quantity on their cabinets.
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Additional info for Annual Plant Reviews, Biochemistry of Plant Secondary Metabolism (Volume 40, 2) (2nd Edition)
F. (1981) Enzymic synthesis of coniceine in Conium maculatum chloroplasts and mitochondria. , 1, 10–13. Saito, K. and Murakoshi, I. F. Roberts and M. Wink). Plenum, New York, pp. 147–57. Sch¨afer, H. and Wink, M. (2009) Medicinally important secondary metabolites in recombinant microorganisms or plants: Progress in alkaloid biosynthesis. Biotechnological Journal 4, 1684–1703. S. (1998) Plant Secondary Metabolism. Kluwer, Norwell. , Ueda, K. and Yazaki, Y. (2003) Application of vanadate-induced nucleotide trapping to plant cells for detection of ABC proteins.
3 summarizes the evidence for xylem and phloem transport of some SM. , 1987). In a number of plants, specific idioblasts have been detected that contain tannins, alkaloids or glucosinolates. ) (Wiermann, 1981; Wink, 1993, 1997; Wink and Roberts, 1998). Flowers, fruits and seeds are usually rich in SM, especially in annual plants. In perennial species, high amounts of SM are found in bulbs, roots, rhizomes and the bark of roots and stems. Several SM are not end products of metabolism, but are turned over at ¨ a regular rate (Barz and Koster, 1981).
1994). These authors also suggested that spermidine may act, at least in part, as a co-substrate with putrescine in homospermidine formation. The apparent rapid interconversion of putrescine and spermidine in these cultures makes this a difficult problem to solve. However, it has been shown that more than half the aminobutyl moiety of homospermidine comes directly from spermine, and the aminobutyl moiety of spermine is also incorporated directly into the necine base of pyrrolizidine alkaloids (Graser and Hartmann, 1997).
Annual Plant Reviews, Biochemistry of Plant Secondary Metabolism (Volume 40, 2) (2nd Edition) by Michael Wink