The Synthesis and Biochemical Use of N‐Hydroxyl‐N‐(5‐aminopentyl)succinamic acid (HSC) by the Enzyme FslA

Applications of N-dimethyl amino succinamic acid to the foliage on six-year-old Gravenstein apples restricted the extension growth. The reduced growth was characterized by shorter internode length giving the trees a more compact appearance. The number of leaves was also reduced although not to the same extent as extension growth. The leaf size was not affected. Two successive applications of 1,000 p.p.m. or a single spray of 2,000 p.p.m. applied early in the growing season resulted in highly significant increase of bloom in the following year. Yields were doubled by both treatments.

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ChemInform Abstract: ELECTRON SPIN RESONANCE STUDIES OF IRRADIATED SUCCINAMIC ACID PART 1 AND 2, TRICLINIC SINGLE CRYSTALS, MONOCLINIC SINGLE CRYSTALS

Chemischer Informationsdienst ◽

10.1002/chin.197424067 ◽

1974 ◽

Vol 5 (24) ◽

Author(s):

D. C. STRAW ◽

GRACE C. MOULTON

Keyword(s):

Electron Spin Resonance ◽

Single Crystals ◽

Electron Spin ◽

Succinamic Acid ◽

Spin Resonance

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N-(3-Chloro-2-methylphenyl)succinamic acid

Acta Crystallographica Section E Structure Reports Online ◽

10.1107/s1600536812022763 ◽

2012 ◽

Vol 68 (6) ◽

pp. o1869-o1869

Author(s):

B. Thimme Gowda ◽

Sabine Foro ◽

U. Chaithanya

Keyword(s):

Hydrogen Bonds ◽

Benzene Ring ◽

Dihedral Angle ◽

Title Compound ◽

Amide Group ◽

Compound C ◽

Succinamic Acid

In the title compound, C11H12ClNO3, the dihedral angle between the benzene ring and the amide group is 44.9 (2)°. In the crystal, molecules form inversion dimers via pairs of O—H...O hydrogen bonds. These dimers are further linked into sheets parallel to (013) via N—H...O hydrogen bonds.

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N-2-Fluorenyl Succinamic Acid 59935-47-6

Sax's Dangerous Properties of Industrial Materials ◽

10.1002/0471701343.sdp12459 ◽

2004 ◽

Keyword(s):

Succinamic Acid

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N,N-Dipropyl Succinamic Acid Ethyl Ester 10143-31-4

Sax's Dangerous Properties of Industrial Materials ◽

10.1002/0471701343.sdp36279 ◽

2012 ◽

Keyword(s):

Ethyl Ester ◽

Acid Ethyl Ester ◽

Succinamic Acid

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New Substrates for the Dicarboxylate Transport System of Sinorhizobium meliloti

Journal of Bacteriology ◽

10.1128/jb.182.15.4216-4221.2000 ◽

2000 ◽

Vol 182 (15) ◽

pp. 4216-4221 ◽

Cited By ~ 21

Author(s):

Svetlana Yurgel ◽

Michael W. Mortimer ◽

Kimberly N. Rogers ◽

Michael L. Kahn

Keyword(s):

Dicarboxylic Acid ◽

Transport System ◽

Sinorhizobium Meliloti ◽

Monocarboxylic Acid ◽

Dicarboxylic Acids ◽

Carbonyl Groups ◽

Nitrogen Fixing ◽

Extended Conformation ◽

Dicarboxylate Transport ◽

Succinamic Acid

ABSTRACT The dicarboxylate transport (Dct) system of Sinorhizobium meliloti, which is essential for a functional nitrogen-fixing symbiosis, has been thought to transport only dicarboxylic acids. We show here that the permease component of the Dct system, DctA, can transport orotate, a monocarboxylic acid, with an apparentKm of 1.7 mM and a V maxof 163 nmol min−1 per mg of protein in induced cells. DctA was not induced by the presence of orotate. The transport of orotate was inhibited by several compounds, including succinamic acid and succinamide, which are not dicarboxylic acids. The dicarboxylic acid maleate (cis-butenedioic acid) was not an inhibitor of orotate transport, which suggests that it was not recognized by DctA. However, maleate was an excellent inducer of DctA expression. Our evaluation of 17 compounds as inducers and inhibitors of transport suggests that substrates recognized by S. meliloti DctA must have appropriately spaced carbonyl groups and an extended conformation, while good inducers are more likely to have a curved conformation.

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