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  2. Phenylglycine - Wikipedia

    en.wikipedia.org/wiki/Phenylglycine

    Phenylglycine is the organic compound with the formula C 6 H 5 CH(NH 2)CO 2 H. It is a non-proteinogenic alpha amino acid related to alanine, but with a phenyl group in place of the methyl group. It is a white solid. The compound exhibits some biological activity. [1]

  3. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    [citation needed] Decomposition of dead plant material causes complex organic compounds to be slowly oxidized lignin-like humus or to break down into simpler forms (sugars and amino sugars, aliphatic and phenolic organic acids), which are further transformed into microbial biomass (microbial humus) or are reorganized, and further oxidized, into ...

  4. N-Phenylglycine - Wikipedia

    en.wikipedia.org/wiki/N-Phenylglycine

    N-Phenylglycine is an organic compound with the formula C 6 H 5 NHCH 2 CO 2 H. This white solid achieved fame as the industrial precursor to indigo dye . [ 1 ] It is a non-proteinogenic alpha amino acid related to sarcosine , but with an N - phenyl group in place of N - methyl .

  5. Burkholderia gladioli - Wikipedia

    en.wikipedia.org/wiki/Burkholderia_gladioli

    Burkholderia gladioli is a species of aerobic gram-negative rod-shaped bacteria [1] that causes disease in both humans and plants. It can also live in symbiosis with plants and fungi [2] and is found in soil, water, the rhizosphere, and in the microbiome of many animals. It was formerly known as Pseudomonas marginata.

  6. Plant pathology - Wikipedia

    en.wikipedia.org/wiki/Plant_pathology

    Toxins: These can be non-host-specific, which damage all plants, or host-specific, which cause damage only on a host plant. Effector proteins: These can be secreted by pathogens such as bacteria, fungi, and oomycetes [6] [7] into the extracellular environment or directly into the host cell, often via the Type three secretion system. Some ...

  7. Plant secondary metabolism - Wikipedia

    en.wikipedia.org/wiki/Plant_secondary_metabolism

    The compounds of these secondary metabolites (As seen in Figure 1) are found in over 2000 plant species. Its structure allows the release of cyanide, a poison produced by certain bacteria, fungi, and algae that is found in numerous plants. Animals and humans possess the ability to detoxify cyanide from their systems naturally.

  8. Xylella fastidiosa - Wikipedia

    en.wikipedia.org/wiki/Xylella_fastidiosa

    Significant variation in symptoms is seen between diseases, though some symptoms are expressed across species. On a macroscopic scale, plants infected with a X. fastidiosa-related disease exhibit symptoms of water, zinc, and iron deficiencies, [27] manifesting as leaf scorching and stunting in leaves turning them yellowish-brown, gummy substance around leaves, [27] fruit reduction in size and ...

  9. Pseudomonas syringae - Wikipedia

    en.wikipedia.org/wiki/Pseudomonas_syringae

    The bacteria tend to be seed-borne, and are dispersed between plants by rain splash. [18] Although it is a plant pathogen, it can also live as a saprotroph in the phyllosphere when conditions are not favourable for disease. [19] Some saprotrophic strains of P. syringae have been used as biocontrol agents against postharvest rots. [20]