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Secondary metabolite number

A considerable number of mycotoxins that show high toxicity to vertebrates and/ or invertebrates are produced by organisms associated with crop plants (Flannigan 1991). There are many known cases of human poisoning caused by such compounds. There are three broad categories of mycotoxins represented here, based on the structures of the intermediates from which these secondary metabolites are derived. They are (1) compounds derived from polyketides, (2) terpenes derived from mevalonic acid, and (3) cyclic peptides and derivatives thereof. [Pg.13]

The effect of a particular cultivation environment on a system can be evaluated in terms of biomass (fresh/dry weight, cell number), secondary metabolite production [51,75,89,102,103,106,107] or substrate consumption (e.g. carbon source [57] or oxygen [53,108]). Using the Evan s Blue method to identify non-viable cells. Ho et al. [108] used viable cell density measurements to determine variations in specific growth rate attributable to hydrodynamic stress. [Pg.150]

The occurrence in some plants of secondary metabolites characterized by an 0-heterocyclic structure and exhibiting antimicrobial properties is a well-known phenomenon [2,8-10]. Among them, catechins and proanthocyanidins are two classes of compounds exhibiting antimicrobial properties towards both prokaryotic and eukaryotic microorganisms. Yet, despite the large number of studies published so far, the real potentialities and limitations given by the use of this class of molecules as antiviral or antimicrobial (antibacterial, antimycotic, antiprotozoal) agents have not been critically evaluated. The present chapter represents an overview of the re-... [Pg.240]

I. PRODUCTION OF ANTIBIOTICS. The production of secondary metabolites with antimicrobial properties has long been recognized as an important factor in disease suppression (see Chap. 7). Metabolites with biocontrol properties have been isolated from a large number of rhizosphere microorganisms, including the fluorescent pseudomonads (Table 2). Further discussion is not given here since this is the subject of recent reviews (122,123). [Pg.108]

A number of polypeptide biomarkers have also been identified in the mass range below 4000,28-31 which are cyclic secondary metabolites bonded to lipids or sugars. These peptide sequences are not directly translated from DNA,32... [Pg.258]

Polyphenols are the most abundant antioxidants in human diets. They are secondary metabolites of plants. These compounds are designed with an aromatic ring carrying one or more hydroxyl moieties. Several classes can be considered according to the number of phenol rings and to the structural elements that bind these rings. [Pg.53]

Horseradish peroxidase (HRP) is an extracellular plant enzyme that acts in regulation of cell growth and differentiation, polymerization of cell wall components, and the oxidation of secondary metabolites essential for important pathogenic defense reactions. Because of these essential functions, and also because of its stability and ready availability, HRP has attracted considerable attention.13 It has been involved in a number of applications, such as diagnostic assays,14 biosensors,15 bioremediation,16 polymer synthesis,17 and other biotechnological processes.18 More applications in which HRP catalysis is translated into an electrochemical signal are likely to be developed in the near future. [Pg.311]

Aryl side chain containing L-a-amino acids, such as phenylalanine (Phe), tyrosine (Tyr), and tryptophan (Trp), are derived through the shikimate pathway. The enzymatic transformation of phosphoenolpyr-uvate (PEP) and erythro-4-phosphate, through a series of reactions, yields shikimate (Scheme 2). Although shikimate is an important biosynthetic intermediate for a number of secondary metabolites, this chapter only describes the conversion of shikimate to amino acids containing aryl side chains. In the second part of the biosynthesis, shikimate is converted into chorismate by the addition of PEP to the hydroxyl group at the C5 position. Chorismate is then transformed into prephenate by the enzyme chorismate mutase (Scheme 3). [Pg.7]

Fortunately, of the vast number of mushroom species that exists, only a few produce secondary metabolites that cause fatal poisonings. If toxins causing benign symptoms, such as abdominal pain and diarrhea, hallucinations, or alcohol incompatibility, are disregarded, the most significant mushroom toxins are the extremely hazardous compounds of amatoxins, orellanine, and, to a lesser extent, methylhydrazine and its derivatives. Consequently, there is only a... [Pg.87]


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See also in sourсe #XX -- [ Pg.1015 ]

See also in sourсe #XX -- [ Pg.251 ]




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Secondary metabolites

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