NCBI Taxonomy: 193

Azospirillum lipoferum (ncbi_taxid: 193)

found 58 associated metabolites at species taxonomy rank level.

Ancestor: Azospirillum

Child Taxonomies: Azospirillum lipoferum 4B

Gibberellin A3

(1S,2S,4aR,4bR,7S,9aS,10S,10aR)-2,7-dihydroxy-1-methyl-8-methylidene-13-oxo-1,2,4b,5,6,7,8,9,10,10a-decahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid

C19H22O6 (346.1416312)


Gibberellic acid, also known as gibberellin A3, GA, or GA3, is a very potent hormone whose natural occurrence in plants controls their development. Since GA regulates growth, applications of very low concentrations can have a profound effect while too much will have the opposite effect. Gibberellic acid is a hormone found in plants. Gibberellic acid is a simple gibberellin promoting the growth and elongation of cells. It affects the decomposition of plants. It also helps plants grow if used in small amounts but eventually, plants grow a tolerance for it. Gibberellic acid stimulates the cells of germinating seeds to produce mRNA molecules that code for hydrolytic enzymes. Gibberellic acid is a white powder. (NTP, 1992) Gibberellin A3 is a C19-gibberellin that is a pentacyclic diterpenoid responsible for promoting growth and elongation of cells in plants. Initially identified in Gibberella fujikuroi,it differs from gibberellin A1 in the presence of a double bond between C-3 and C-4. It has a role as a plant metabolite and a mouse metabolite. It is a lactone, a gibberellin monocarboxylic acid, an organic heteropentacyclic compound and a C19-gibberellin. It is a conjugate acid of a gibberellin A3(1-). Gibberellic acid is a natural product found in Cocos nucifera, Prunus cerasus, and other organisms with data available. Gibberellins (GAs) are plant hormones that regulate growth and influence various developmental processes, including stem elongation, germination, dormancy, flowering, sex expression, enzyme induction, and leaf and fruit senescence. Gibberellins is found in many foods, some of which are common wheat, potato, sunflower, and common pea. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D005875 - Gibberellins CONFIDENCE standard compound; INTERNAL_ID 449; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3262; ORIGINAL_PRECURSOR_SCAN_NO 3260 CONFIDENCE standard compound; INTERNAL_ID 449; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3253; ORIGINAL_PRECURSOR_SCAN_NO 3251 CONFIDENCE standard compound; INTERNAL_ID 449; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3271; ORIGINAL_PRECURSOR_SCAN_NO 3269 CONFIDENCE standard compound; INTERNAL_ID 449; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3249; ORIGINAL_PRECURSOR_SCAN_NO 3246 CONFIDENCE standard compound; INTERNAL_ID 449; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3255; ORIGINAL_PRECURSOR_SCAN_NO 3254 KEIO_ID G074 Gibberellic Acid is named after a fungus Gibberella fujikuroi . Gibberellic Acid regulates processes of plant development and growth, including seed development and germination, stem and root growth, cell division, and flowering time[1]. Gibberellic Acid is named after a fungus Gibberella fujikuroi . Gibberellic Acid regulates processes of plant development and growth, including seed development and germination, stem and root growth, cell division, and flowering time[1].

   

3-Epigibberellin A1

(1R,2R,5S,8S,9S,10R,11S,12R)-5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

C19H24O6 (348.1572804)


3-Epigibberellin A1 (3-epi-GA1), belongs to the class of organic compounds known as C19-gibberellin 6-carboxylic acids. These are C19-gibberellins with a carboxyl group at the 6-position. 3-Epigibberellin A1 is found in green vegetables. 3-Epigibberellin A1 is a constituent of Lactuca sativa (lettuce). Constituent of Lactuca sativa (lettuce). 3-Epigibberellin A1 is found in green vegetables.

   

N-hexanoyl-L-Homoserine lactone

N-[(3S)-tetrahydro-2-oxo-3-furanyl]-hexanamide

C10H17NO3 (199.1208372)


N-Hexanoyl-L-homoserine lactone (HHSL) is a type of signaling molecule known as an autoinducer, which plays a significant role in bacterial communication and behavior, particularly in processes governed by quorum sensing (QS). Here are some of its key biological functions: Quorum Sensing Signaling: HHSL is involved in quorum sensing, a mechanism by which bacteria communicate with each other to coordinate their behavior based on population density. When the concentration of HHSL reaches a certain threshold, it triggers specific responses in the bacterial population. Regulation of Gene Expression: In many bacteria, HHSL binds to specific transcriptional regulators, leading to the activation or repression of target genes. This regulation can control a variety of biological processes, including bioluminescence, biofilm formation, virulence factor production, and sporulation. Biofilm Formation: HHSL can influence the formation and maintenance of biofilms, which are complex communities of bacteria encased in a self-produced matrix. Biofilms are often associated with increased resistance to antibiotics and host immune responses. Virulence and Pathogenicity: In pathogenic bacteria, HHSL can regulate the expression of virulence factors, contributing to the bacteria’s ability to cause disease. By modulating these factors, HHSL can affect the bacteria’s interaction with the host and its ability to evade the immune system. Symbiotic Interactions: HHSL is not only important in pathogenic bacteria but also in beneficial interactions, such as those found in nitrogen-fixing bacteria or in symbiotic relationships with plants and animals. Understanding the role of HHSL and other autoinducers in bacterial communication and behavior is crucial for developing new strategies to control bacterial infections and manage biofilm-related issues.

   

N-Octanoyl-DL-homoserine lactone

N-(2-Oxotetrahydrofuran-3-YL)octanamide

C12H21NO3 (227.1521356)


   

OOHL

3-Oxo-octanoic acid (2-oxo-tetrahydro-furan-3-YL)-amide

C12H19NO4 (241.1314014)


   

N-(3-Oxohexanoyl)homoserine lactone

3-oxo-N-[(3S)-tetrahydro-2-oxo-3-furanyl]-hexanamide

C10H15NO4 (213.100103)


   

Gibberellins

5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadec-13-ene-9-carboxylic acid

C19H22O6 (346.1416312)


Gibberellic acid is a very potent hormone whose natural occurrence in plants controls their development. Since GA regulates growth, applications of very low concentrations can have a profound effect while too much will have the opposite effect. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D005875 - Gibberellins

   

Gibberellin A1

4a?,4b?-Gibbane-1?,10?-dicarboxylic acid, 2?,4a,7-trihydroxy-1-methyl-8-methylene-, 1,4a-lactone (8CI); 4a,1-(Epoxymethano)-7,9a-methanobenz[a]azulene, gibbane-1,10-dicarboxylic acid deriv.; (+)-Gibberillin A1; GA1; Giberellin A1

C19H24O6 (348.1572804)


Gibberellin A1 is a C19-gibberellin, initially identified in Gibberella fujikuroi. It has a role as a plant metabolite. It is a lactone, a gibberellin monocarboxylic acid and a C19-gibberellin. It is a conjugate acid of a gibberellin A1(1-). Gibberellin A1 is a natural product found in Thlaspi arvense, Populus candicans, and other organisms with data available. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D005875 - Gibberellins A C19-gibberellin, initially identified in Gibberella fujikuroi. Gibberellin a1, also known as ga1, is a member of the class of compounds known as c19-gibberellin 6-carboxylic acids. C19-gibberellin 6-carboxylic acids are c19-gibberellins with a carboxyl group at the 6-position. Thus, gibberellin a1 is considered to be an isoprenoid lipid molecule. Gibberellin a1 is slightly soluble (in water) and a weakly acidic compound (based on its pKa). Gibberellin a1 can be found in a number of food items such as elderberry, enokitake, black salsify, and new zealand spinach, which makes gibberellin a1 a potential biomarker for the consumption of these food products.

   

Pseudogibberellin a1

5,12-dihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

C19H24O6 (348.1572804)


   

3-Oxo-N-[(3s)-2-Oxotetrahydrofuran-3-Yl]decanamide

3-Oxo-N-[(3s)-2-Oxotetrahydrofuran-3-Yl]decanamide

C14H23NO4 (269.1626998)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

N-[(3s)-2-Oxotetrahydrofuran-3-Yl]decanamide

N-[(3s)-2-Oxotetrahydrofuran-3-Yl]decanamide

C14H25NO3 (255.183434)


   

N-(2-Oxotetrahydrofuran-3-YL)octanamide

N-(2-Oxotetrahydrofuran-3-YL)octanamide

C12H21NO3 (227.1521356)


   

gibberellin A3

gibberellin A3

C19H22O6 (346.1416312)


A C19-gibberellin that is a pentacyclic diterpenoid responsible for promoting growth and elongation of cells in plants. Initially identified in Gibberella fujikuroi,it differs from gibberellin A1 in the presence of a double bond between C-3 and C-4.

   

3-hydroxy-n-(2-oxooxolan-3-yl)octanimidic acid

3-hydroxy-n-(2-oxooxolan-3-yl)octanimidic acid

C12H21NO4 (243.1470506)


   

3-oxo-n-(2-oxooxolan-3-yl)octanimidic acid

3-oxo-n-(2-oxooxolan-3-yl)octanimidic acid

C12H19NO4 (241.1314014)


   

n-[(3s)-2-oxooxolan-3-yl]hexanimidic acid

n-[(3s)-2-oxooxolan-3-yl]hexanimidic acid

C10H17NO3 (199.1208372)


   

3-oxo-n-[(3s)-2-oxooxolan-3-yl]hexanimidic acid

3-oxo-n-[(3s)-2-oxooxolan-3-yl]hexanimidic acid

C10H15NO4 (213.100103)


   

3-oxo-n-(2-oxooxolan-3-yl)hexanimidic acid

3-oxo-n-(2-oxooxolan-3-yl)hexanimidic acid

C10H15NO4 (213.100103)


   

(3s)-3-hydroxy-n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

(3s)-3-hydroxy-n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

C14H25NO4 (271.178349)


   

n-(2-oxooxolan-3-yl)hexanimidic acid

n-(2-oxooxolan-3-yl)hexanimidic acid

C10H17NO3 (199.1208372)


   

(3s)-3-hydroxy-n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

(3s)-3-hydroxy-n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

C12H21NO4 (243.1470506)


   

3-oxo-n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

3-oxo-n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

C14H23NO4 (269.1626998)


   

n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

n-[(3s)-2-oxooxolan-3-yl]decanimidic acid

C14H25NO3 (255.183434)


   

3-oxo-n-(2-oxooxolan-3-yl)decanimidic acid

3-oxo-n-(2-oxooxolan-3-yl)decanimidic acid

C14H23NO4 (269.1626998)


   

n-(2-oxooxolan-3-yl)decanimidic acid

n-(2-oxooxolan-3-yl)decanimidic acid

C14H25NO3 (255.183434)


   

3-hydroxy-n-(2-oxooxolan-3-yl)decanimidic acid

3-hydroxy-n-(2-oxooxolan-3-yl)decanimidic acid

C14H25NO4 (271.178349)


   

3-oxo-n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

3-oxo-n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

C12H19NO4 (241.1314014)


   

n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

n-[(3s)-2-oxooxolan-3-yl]octanimidic acid

C12H21NO3 (227.1521356)