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Journal articles on the topic '6-hydroxyhexanoic acid'

Author: Grafiati
Published: 4 June 2021
Last updated: 9 February 2022

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1

Srinivasamurthy, Vishnu S. T., Dominique Böttcher, and Uwe T. Bornscheuer. "A multi-enzyme cascade reaction for the production of 6-hydroxyhexanoic acid." Zeitschrift für Naturforschung C 74, no. 3-4 (2019): 71–76. http://dx.doi.org/10.1515/znc-2018-0216.

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Abstract Multi-enzyme cascade reactions capture the essence of nature’s efficiency by increasing the productivity of a process. Here we describe one such three-enzyme cascade for the synthesis of 6-hydroxyhexanoic acid. Whole cells of Escherichia coli co-expressing an alcohol dehydrogenase and a Baeyer-Villiger monooxygenase (CHMO) for internal cofactor regeneration were used without the supply of external NADPH or NADP+. The product inhibition caused by the ε-caprolactone formed by the CHMO was overcome by the use of lipase CAL-B for in situ conversion into 6-hydroxyhexanoic acid. A stirred t
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2

Pyo, Sang-Hyun, Ji Hoon Park, Vanessa Srebny та Rajni Hatti-Kaul. "A sustainable synthetic route for biobased 6-hydroxyhexanoic acid, adipic acid and ε-caprolactone by integrating bio- and chemical catalysis". Green Chemistry 22, № 14 (2020): 4450–55. http://dx.doi.org/10.1039/d0gc01454k.

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A green synthetic route and possible utilization of biobased 6-carbon polymer building blocks 6-hydroxyhexanoic acid, adipic acid and ε-caprolactone from biomass via 1,6-hexanediol, a hydrogenation product of biobased 5-hydroxymethylfurfural.
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3

Knopik, Pawel, Karol S. Bruzik, and Wojciech J. Stec. "AN IMPROVED SYNTHESIS OF 6-(O-PHOSPHORYLCHOLINE)HYDROXYHEXANOIC ACID." Organic Preparations and Procedures International 23, no. 2 (1991): 214–16. http://dx.doi.org/10.1080/00304949109458318.

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4

Liang, Yiru, Yu Zhang, Yujing Hu, Bo Xia, Xianfu Lin, and Qi Wu. "Lipase-catalyzed synthesis of chiral poly(ester amide)s with an alternating sequence of hydroxy acid and l/d-aspartate units." Polymer Chemistry 9, no. 12 (2018): 1412–20. http://dx.doi.org/10.1039/c7py01936j.

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Alternating poly(hydroxyhexanoic acid-alt-l/d-β-aspartate)s with α-benzyl or α-methyl ester side groups were prepared via the enzymatic polycondensation of N-(6-hydroxyhexanoyl) l/d-aspartate diesters.
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5

KNOPIK, P., K. S. BRUZIK, and W. J. STEC. "ChemInform Abstract: An Improved Synthesis of 6-(O-Phosphorylcholine)hydroxyhexanoic Acid." ChemInform 22, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199145226.

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6

Tang, Xiaofang, Jing You, Di Liu, Ming Xia, Liyu He, and Hong Liu. "5-Hydroxyhexanoic Acid Predicts Early Renal Functional Decline in Type 2 Diabetes Patients with Microalbuminuria." Kidney and Blood Pressure Research 44, no. 2 (2019): 245–63. http://dx.doi.org/10.1159/000498962.

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Background/Aims: Diabetic nephropathy (DN) is a leading cause of end-stage renal disease. Microalbuminuria (MA) is widely used to predict early progressive renal function decline (ERFD) of DN in type 2 diabetes mellitus (T2D) patients, but the sensitivity and specificity of MA have been questioned. Here, we determined the urine metabolites differences between T2D patients with MA who maintained stable renal function and those who progressed to ERFD in order to identify specific biomarkers of the progression of renal dysfunction. Methods: A total of 102 T2D patients with MA and normal renal fun
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7

Abe, Hideki, Hiromichi Aoki, and Yoshiharu Doi. "Morphologies and enzymatic degradability of melt-crystallized poly(3-hydroxybutyric acid-Co -6-hydroxyhexanoic acid)." Macromolecular Symposia 130, no. 1 (1998): 81–89. http://dx.doi.org/10.1002/masy.19981300108.

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8

Wolinsky, Jesse B., William C. Ray, Yolonda L. Colson, and Mark W. Grinstaff. "Poly(carbonate ester)s Based on Units of 6-Hydroxyhexanoic Acid and Glycerol." Macromolecules 40, no. 20 (2007): 7065–68. http://dx.doi.org/10.1021/ma071276v.

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9

Seo, Young-Man, Aran Kim, Han-Seop Bea, Sang-Hyeup Lee, and Hyungdon Yun. "Asymmetric synthesis ofl-6-hydroxynorleucine from 2-keto-6-hydroxyhexanoic acid using a branched-chain aminotransferase." Biocatalysis and Biotransformation 30, no. 2 (2011): 171–76. http://dx.doi.org/10.3109/10242422.2011.638373.

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10

Abe, Hideki, Yoshihiro Kikkawa, Hiromichi Aoki, Takashi Akehata, Tadahisa Iwata, and Yoshiharu Doi. "Crystallization behavior and thermal properties of melt-crystallized poly[(R)-3-hydroxybutyric acid-co-6-hydroxyhexanoic acid] films." International Journal of Biological Macromolecules 25, no. 1-3 (1999): 177–83. http://dx.doi.org/10.1016/s0141-8130(99)00032-x.

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11

Martínez-Palau, Meritxell, Lourdes Franco, and Jordi Puiggalí. "Isothermal crystallization of poly(glycolic acid-alt-6-hydroxyhexanoic acid) studied by DSC and real time synchrotron SAXS/WAXD." Polymer 48, no. 20 (2007): 6018–28. http://dx.doi.org/10.1016/j.polymer.2007.08.001.

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12

Morales, Laura, Lourdes Franco, MarÍA Teresa Casas, and Jordi PuiggalÍ. "Crystallization behavior of clay nanocomposites prepared from a degradable alternating copolyester constituted by glycolic acid and 6-hydroxyhexanoic acid." Journal of Polymer Science Part B: Polymer Physics 48, no. 1 (2009): 33–46. http://dx.doi.org/10.1002/polb.21841.

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13

Borzenkov, Mykola, Natalia Mitina, Volodymyr Lobaz, and Orest Hevus. "Synthesis and Properties of Novel Surface Active Monomers Based on Derivatives of 4-Hydroxybutyric Acid and 6-Hydroxyhexanoic Acid." Journal of Surfactants and Detergents 18, no. 1 (2014): 133–44. http://dx.doi.org/10.1007/s11743-014-1640-z.

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14

Schirmer, Andreas, Claudia Matz, and Dieter Jendrossek. "Substrate specificities of poly(hydroxyalkanoate)-degrading bacteria and active site studies on the extracellular poly(3-hydroxyoctanoic acid) depolymerase of Pseudomonas fluorescens GK13." Canadian Journal of Microbiology 41, no. 13 (1995): 170–79. http://dx.doi.org/10.1139/m95-184.

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The isolation of poly(3-hydroxyoctanoic acid)- and poly(6-hydroxyhexanoic acid)-degrading bacteria yielded 28 strains with abilities to degrade various polymers. The most versatile strains hydrolyzed five different polyesters comprising short chain length and medium chain length poly(hydroxyalkanoates). The new isolates together with previously isolated poly(hydroxyalkanoate)-degrading bacteria were classified into 11 groups with respect to their polymer-degrading specificities. All PHA depolymerases studied so far have been characterized by the lipase consensus sequence Gly-X-Ser-X-Gly in the
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15

Kikkawa, Y., Y. Inoue, H. Abe, T. Iwata, and Y. Doi. "In situ observation of lamellar growth in thin films for poly[( R )-3-hydroxybutyric acid- co -6-hydroxyhexanoic acid] at a high crystallization temperature of 110°C by atomic force microscopy." Polymer 42, no. 6 (2001): 2707–10. http://dx.doi.org/10.1016/s0032-3861(00)00599-1.

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16

Nesterova, Oksana V., Maximilian N. Kopylovich, and Dmytro S. Nesterov. "A Comparative Study of the Catalytic Behaviour of Alkoxy-1,3,5-Triazapentadiene Copper(II) Complexes in Cyclohexane Oxidation." Inorganics 7, no. 7 (2019): 82. http://dx.doi.org/10.3390/inorganics7070082.

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The mononuclear copper complexes [Cu{NH=C(OR)NC(OR)=NH}2] with alkoxy-1,3,5-triazapentadiene ligands that have different substituents (R = Me (1), Et (2), nPr (3), iPr (4), CH2CH2OCH3 (5)) were prepared, characterized (including the single crystal X-ray analysis of 3) and studied as catalysts in the mild oxidation of alkanes with H2O2 as an oxidant, pyridine as a promoting agent and cyclohexane as a main model substrate. The complex 4 showed the highest activity with a yield of products up to 18.5% and turnover frequency (TOF) up to 41 h−1. Cyclohexyl hydroperoxide was the main reaction produc
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17

Gregorowicz, Jacek. "Solubilities of lactic acid and 2-hydroxyhexanoic acid in supercritical CO2." Fluid Phase Equilibria 166, no. 1 (1999): 39–46. http://dx.doi.org/10.1016/s0378-3812(99)00283-6.

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18

Abe, Hideki, Yoshiharu Doi, Hiromichi Aoki, Takashi Akehata, Yoji Hori, and Akio Yamaguchi. "Physical Properties and Enzymic Degradability of Copolymers of (R)-3-Hydroxybutyric and 6-Hydroxyhexanoic Acids." Macromolecules 28, no. 23 (1995): 7630–37. http://dx.doi.org/10.1021/ma00127a007.

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19

Cheng, Xuanying, Diankun Chen, and Chuanxin Xie. "Effect of Metal Ion Modified TS-1 on Cyclization Properties of 6-Hydroxyhexanoic Acid." Catalysis Letters, March 13, 2021. http://dx.doi.org/10.1007/s10562-021-03546-3.

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20

Bretschneider, Lisa, Ingeborg Heuschkel, Martin Wegner, et al. "Conversion of Cyclohexane to 6-Hydroxyhexanoic Acid Using Recombinant Pseudomonas taiwanensis in a Stirred-Tank Bioreactor." Frontiers in Catalysis 1 (May 21, 2021). http://dx.doi.org/10.3389/fctls.2021.683248.

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6-hydroxyhexanoic acid (6HA) represents a polymer building block for the biodegradable polymer polycaprolactone. Alternatively to energy- and emission-intensive multistep chemical synthesis, it can be synthesized directly from cyclohexane in one step by recombinant Pseudomonas taiwanensis harboring a 4-step enzymatic cascade without the accumulation of any intermediate. In the present work, we performed a physiological characterization of this strain in different growth media and evaluated the resulting whole-cell activities. RB and M9* media led to reduced gluconate accumulation from glucose
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