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Biosynthesis leaves

At the present time about 3,000 alkaloids are known which are distributed among almost 4,000 plant species. In view of their profusion, it is not surprising that not all of the compounds that are usually considered as alkaloids meet fully the definition given above. Alkaloids are also not limited to plants a few have been demonstrated in animal organisms. Furthermore, not all compounds so classified are basic. Exceptions to this rule are, for example, nicotinic acid, colchicine and the betacyanins. Finally, the N is not always contained in a heterocycle, as can be seen from the structural formula of colchicine. However, these exceptions are usually included in the alkaloids because their biosynthesis leaves no doubt as to their close relationship to true alkaloids. [Pg.144]

Enzymes. The enzymes most important to the chemistry and manufacturing of tea are those responsible for the biosynthesis of tea flavonoids (Table 4) and those involved in the conversion of fresh leaf into manufactured commercial teas. [Pg.368]

Suzuki, T. and Takahashi, E., Biosynthesis of caffeine by tea-leaf extracts, Biochemistry, 146,87,1975. [Pg.21]

Jha, A.K., Prasad, K., Kumar, V. and Prasad, K. (2009) Biosynthesis of silver nanoparticles using Eclipta leaf. Biotechnology Progress, 25, 1476-1479. [Pg.238]

Fig. 3 Biosynthetic pathways to pyrethrins. The identified enzymes involved in biosynthesis are shown in orange. Note that green leaf volatiles and the plant hormone jasmonic acid share the oxylipin pathway. The phosphate moiety is indicated as P ... Fig. 3 Biosynthetic pathways to pyrethrins. The identified enzymes involved in biosynthesis are shown in orange. Note that green leaf volatiles and the plant hormone jasmonic acid share the oxylipin pathway. The phosphate moiety is indicated as P ...
There was proposed a detailed account of iridoid biosynthesis in rove beetles which resembles the biosynthesis in leaf beetle larvae but exhibits distinct stereochemical differences [134], see also the chapter by Laurent et al., this volume. [Pg.121]

Theoretically, many of the above discrepancies could be settled by experiments with carboxyl-labeled shikimic acid because this functional group would be lost in the formation of phenylalanine, but retained in the case of a direct conversion to gallic acid. Only ambiguous evidence was obtained, however, from such efforts (10), and it was concluded that at least two pathways for gallic acid biosynthesis must exist (14), with the preferential route depending on leaf age and plant species investigated (15,16). [Pg.110]

Wink, M. and Hartmann, T. 1980. Localization of enzymes of quinolizidine alkaloids biosynthesis in leaf chloroplast of Lupims polyphyllus Lindl. Plant Physiology, 70 lA-11. [Pg.251]

The toxic effects of ozone in plant systems have been studied for some time, yet the actual mechanisms of injury are not fully understood. In addition to visible necrosis which appears largely on upper leaf surfaces, many other physiological and biochemical effects have been recorded ( ). One of the first easily measurable effects is a stimulation of respiration. Frequently, however, respiration may not increase without concomitant visible injury. Furthermore, photosynthesis in green leaves as measured by CO2 assimilation, may decrease. It is well known that ozone exposure is accompanied by a dramatic increase in free pool amino acids ( ). Ordin and his co-workers ( ) have clearly shown the effect of ozone on cell wall biosynthesis. In addition, ozone is known to oxidize certain lipid components of the cell ( ), to affect ribosomal RNA (16) and to alter the fine structure of chloroplasts (7 ). [Pg.8]

Dzhavelidze, T. A. Phenolic compounds in various parts of tea shoots. Subtrop Kult 1978 1978 154-155. Hatanaka, A., T. Kajiwara and J. Sekiya. Biosynthesis of leaf alcohol the oxygenative cleavage of linolenic acid to cis-3-hexenal and 11-formyl-cis-9-undecenoic acid from linolenic acid in tea chloroplasts. Symp Chem Nat Prod-22nd- Fukuoka, Japan 1979 657-664. [Pg.26]

Using the PETIS, real-time [ CJmethionine translocation was studied for barley. For the mechanism of Fe uptake in an Fe-delicient barley, it was found that leaf methionine does not participate in the reaction of mugineic acid synthesis, but the methionine produced in barley roots is used in the biosynthesis of mugineic acid phytosiderophores [131,132]. [Pg.854]

Laing, W. A., Wright, M. A., Cooney, J., Bulley, S. M. (2007). The missing step of the L-galactose pathway of aseorbate biosynthesis in plants, an L-galactose guanyltransferase, increases leaf ascorbate content. Proceedings of the National Academy of Sciences of the United States of America, 104(22), 9534-9539. [Pg.420]

Other naturally derived aflatoxin inhibitors obtained from the "neem" tree have been investigated in our laboratory (84), Azadirachta indica Juss. commonly known as "margosa" or "neem" is an ornamental tree of Asia and Africa that produces natural products having reputed value for their medicinal, antiviral, antibacterial, insecticidal, antifungal and antinematode properties (86, 87). Several active principles from different parts of the neem tree have been reported (88). Our investigation (84) examined the effects of these neem leaf components in neem leaves on aflatoxin biosynthesis by either Aspergillus parasiticus or A. flavus. [Pg.285]

Inhibition of aflatoxin biosynthesis by neem extracts in fungal cells appear to occur in the very early stages of the biosynthetic pathway (i.e., prior to norsolorinic acid synthesis) because after the initiation of secondary metabolism, the inhibitory effect of the neem leaf constituents was lost (84). [Pg.286]


See other pages where Biosynthesis leaves is mentioned: [Pg.146]    [Pg.251]    [Pg.112]    [Pg.47]    [Pg.122]    [Pg.813]    [Pg.164]    [Pg.265]    [Pg.59]    [Pg.61]    [Pg.238]    [Pg.19]    [Pg.212]    [Pg.194]    [Pg.1359]    [Pg.132]    [Pg.78]    [Pg.256]    [Pg.106]    [Pg.195]    [Pg.199]    [Pg.160]    [Pg.168]    [Pg.548]    [Pg.563]    [Pg.134]    [Pg.314]    [Pg.151]    [Pg.399]    [Pg.399]    [Pg.401]    [Pg.408]    [Pg.410]    [Pg.578]    [Pg.1359]    [Pg.314]    [Pg.285]    [Pg.286]    [Pg.194]    [Pg.124]   
See also in sourсe #XX -- [ Pg.148 ]

See also in sourсe #XX -- [ Pg.41 , Pg.148 ]




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