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Plant labeling

Design of human-machine interfaces (e.g., process information displays, alarm systems, plant labeling)... [Pg.361]

Have you noticed any changes in the conditions that may have caused you to make errors in the past (e.g., improved procedures, better plant labeling, more effective sharing of experience) ... [Pg.364]

Research must be conducted to determine how the toxin is taken up by the plant and what its effects are on the plant. Labeled toxin may be required initially to determine when and if the plant has taken up the toxin in the field in order to separate the alle-lopathic effect from that caused by plant pathogens. This knowledge would assist identification of the problem in the field as the presence of the inhibitory pseudomonads on roots is Innocuous, because little noticeable effect occurs on the root except the stunting and occasional root deformation. Plant color is not normally affected. [Pg.513]

Biosynthetic pathways are usually worked out by isotopic labelling of potential precursors and we shall mark the label with a coloured blob. If ornithine is labelled with l4C and fed to the plant, labelled hygrine is isolated. [Pg.1416]

Cultural problems produce a wide range of symptoms, so it may be difficult to determine the exact cause. Observe the plant closely, though, and the problem may become apparent. Look for wounds in the stems, stakes or plant labels that are too tight, or teeth marks caused by animals. [Pg.357]

Biosynthetic pathways are usually worked out by isotopic labelling of potential precursors and in the schemes below the isotopically labelled atom is shown with a coloured blob. Some plants—notably the coca plant—produce the simple pyrroUdlne alkaloid hygrine, which we wiil take as an illustration. If ornithine is made with a label at its a position and fed to the plant, labelled hygrine is isolated. If each amino group in ornithine is labelled in turn with N, the a amino group is lost but the y amino group is retained. [Pg.1157]

On the other hand, when [l- C]acetate was fed to this plant, labeled coniine was obtained. In addition, through degradation studies, it was found that the even-numbered carbons of coniine were labeled [4]. Thus, through the experiments described above, it was clarified that although the skeleton of coniine is very similar to that of peDetierine, coniine is biosynthesized through the polyketide pathway instead of fiom lysine, as in the case of pelletierine. These biosynthetic studies on coniine and related alkaloids were reviewed by Leete [5]. [Pg.258]

Preakuammicine (19) serves as an efficient precursor of akuammicine (20) (a class 1 Strychnos alkaloid) and vindoline (9) (an Aspidosperma alkaloid). When labeled stemmadenine (21) (a Strychnos alkaloid) (class 1) was fed to Catharanthus roseus plants, labeled tabersonine (24) (class 1), vindoline (9) (class 3), and catharanthine (10) (class 5) were produced. Thus, preakuammacine (19) and stemmadenine (21) serve as key intermediates of both class 3 and 5 alkaloids. It has been proposed that incorporation of stemmadenine (21) into vindoline (9) and catharanthine (10) proceeds via dehydrosecodine (25). A Diels-Alder reaction could lead to the formation of tabersonine (24) and catharanthine (10), respectively (Fig. 34.5). [Pg.632]

On in-plant labeling, pictograms must have a red border. [Pg.45]

Employers who use general, nonspecific in-plant labeling systems such as HMIS or NFPA must ensure through their hazard communication program that their employees can correlate the visual warning on the in-plant container with the applicable chemical and its appropriate hazard warnings. [Pg.166]

This also makes training easier because you only need to explain one system of labels. OSHA recommends that if you are using an in-plant labeling system for uniformity, allow the incoming container labels to remain on the original containers rather than removing them when in-plant labels are added. [Pg.167]

There is indirect evidence that reticuline can be formed in H. canadensis from two isomeric racemic 0-methyllaudanosolines. In this plant labeled racemic reticuline gave 0.9 % incorporation into berberine while 6-mono-0-methyllaudanosoline (CXLII Ri = CH3, R2 = H) gave 2.5% and the 4 -isomer (CXLII Ri = H, R2 = CH3) gave 1.0% incorporation. These figures were considered as indicative of the formation of reticuline from the mono ethers with subsequent incorporation into berberine (168). [Pg.451]

Example During the contract negotiations, the provision of the plant labelling has turned out to be a question at issue. [Pg.78]

The operator insisted on the provision of the labelling at a purchase price that has been repeatedly beaten down. The last contract negotiation did not yield a clear result. The operator submits the contract to the plant manufacturer on the assumption that he will give in. The plant manufacturer accepts the order in writing however, he expresses reservation with regard to the plant labelling. If the employer does not react to this, he is deemed to approve tacitly. This means that the plant manufacturer can claim extra costs in terms of an addition for the provision of the labelling. [Pg.78]

H, = Ph and R = H, R = p-OHCgH4, respectively) when fed to appropriate, intact plants. Labelling experiments indicate the C-1—C-2 bond of the precursor a-amino-acids to be the sole linkage severed during the transformations. Even when attempts to isolate intermediates, of necessity nitrogenous, proved virtually futile, an observed in vivo conversion of aldoximes (63)... [Pg.93]


See other pages where Plant labeling is mentioned: [Pg.342]    [Pg.357]    [Pg.1416]    [Pg.1416]    [Pg.163]    [Pg.28]    [Pg.43]    [Pg.351]    [Pg.7810]    [Pg.7812]    [Pg.1086]    [Pg.167]    [Pg.210]    [Pg.290]    [Pg.163]    [Pg.272]    [Pg.274]    [Pg.128]    [Pg.152]    [Pg.156]   
See also in sourсe #XX -- [ Pg.62 ]




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Labeling of plants

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