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JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC · 2013 · IF 2.823

Resolution of (R, S)-ethyl-2-(4-hydroxyphenoxy) propanoate using lyophilized mycelium of Aspergillus oryzae WZ007

Jian-Yong Zheng,Jia-Yu Wu,Yin-Jun Zhang,Zhao Wang

The mycelium of Aspergillus oryzae WZ007 was successfully developed to kinetic resolution of ( R , S )-ethyl-2-(4-hydroxyphenoxy) propanoate (( R , S )-EHPP) for production of ( R )-ethyl-2-(4-hydroxyphenoxy) propanoate (( R )-EHPP). The key biocatalytic process parameters (pH, temperature, rotation speed and substrate concentration) were optimized. Under the optimum conditions, the optical purity of ( R )-EHPP was improved up to >99% when the conversion was above 49%. A. oryzae WZ007 whole-cell lipase exhibited high reaction capacity, enantioselectivity and good reusability. The tolerable substrate concentration was 0.5   mol/L, and dry mycelium of A. oryzae WZ007 maintains over 80% of its initial activity after eight repeating cycles. Therefore the enzymatic preparation of ( R )-EHPP route was suitable for industrial application.

CAS / MDL: 123-31-9
研究领域: 生物化学 · 微生物学 · 制药工程
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RUSSIAN JOURNAL OF ORGANIC CHEMISTRY · 2025 ·Vol. 61 ·期 2 ·338-345 · IF 0.9

Helical Poly(phenyl isocyanide)-Supported (R,R)-(–)-1,2-Diaminocyclohexane Catalyst for Direct Asymmetric Aldol Reaction

Li Chonglong,Lai Caiyun,Zhan Murong,Zhao Xiaona,Dong Wenyuan,Liu Jiaqi,Wang Peibiao

A novel helical poly(phenyl isocyanide) bearing an ( R,R )-(‒)-1,2-diaminocyclohexane pendant (poly- 2 200 ) was designed and synthesized. Helical poly- 2 200 showed an excellent catalytic performance in the asymmetric aldol reaction between cyclohexanone and 2-(trifluoromethyl)benzaldehyde in ethanol: the reaction product had an enantiomeric excess ( ee ) of 87.8%.

研究领域: 有机化学 · 催化化学
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CHINESE JOURNAL OF POLYMER SCIENCE · 2015 ·Vol. 33 ·期 12 ·1713-1720 · IF 1.835

The stereocomplex formation and phase separation of PLLA/PDLA blends with different optical purities and molecular weights

Shao Jun,Liu Yan-long,Xiang Sheng,Bian Xin-chao,Sun Jing-ru,Li Gao,Chen Xue-si,Hou Hao-qing

In this study, the poly(L-lactide)/poly(D-lactide) (PLLA/PDLA) blends with different optical purities of PLLA and various molecular weights of PDLA are prepared by solution mixing, and the stereocomplex formation and phase separation behaviors of these blends are investigated. Results reveal that optical purity and molecular weight do not vary the crystal structure of PLA stereocomplex (sc) and homochiral crystallites (hc). As the optical purity increasing in the blends, the melting temperature of sc ( T sc ) and the content of sc (Δ H sc ) increased, while the melting temperature of hc ( T hm ) hardly changes, although the content of hc (Δ H hm ) decreased gradually. The T sc and Δ H sc are also enhanced as the molecular weight of PDLA reduces, and the Δ H hm reduces rapidly even though the T hm does not vary apparently. With lower optical purities of PLLA and higher molecular weights of PDLA, three types of crystals form in the blends, i.e. , PLA sc, PLLA hc and PDLA hc. As molecular weight decreases and optical purity enhances, the crystal phase decreases to two (sc and PDLA hc), and one (sc) finally. This investigation indicates that the phase separation behavior between PLLA and PDLA in the PLLA/PDLA blends not only depends on molecular weights, but also relies on the optical purities of polymers.

CAS / MDL: 67-63-0
研究领域: 材料科学 · 高分子化学
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JOURNAL OF CHEMICAL RESEARCH · 2014 · IF 0.697

Efficient Chiral Resolution of (±)-Cyclohexane-1,2-Diamine

Chuan-Zhu Gao,Tian-Shuai Wang,Jia Chen,Fan Fei,Ji Chen,Yan Zhang,Bo Yang

A novel and efficient method has been developed for the chiral resolution and separation from cis-cyclohexane-1,2-diamine of (±)-cyclohexane-1,2-diamine, which reacts with xylaric acid, a substitute for tartaric acid. This method provides (1R,2R)-cyclohexane-1,2-diamine, and (1S,2S)-cyclohexane-1,2-diamine and cis-cyclohexane-1,2-diamine in good yield with high optical purity.

研究领域: 有机化学 · 药物化学
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International Journal of Polymeric Materials and Polymeric Biomaterials · 2018 · IF 2.127

Surface molecularly imprinted material for enantiomeric resolution of ibuprofen: Preparation and study on chiral recognition and resolution property

Baojiao Gao,Yanbin Li,Lulu Chen

The surface imprinted material of one single enantiomer of ibuprofen ((S)-ibuprofen) was successfully prepared using the novel surface imprinting technique of synchronously graft/crosslinking-polymerizing and molecule imprinting. Micron sized-silica gel particles as matrix were first modified with coupling agent γ-mercaptopropyl trimethoxysilane (MPMS), obtaining MPMS-SiO2 particles, on which there was a great deal of mercapto group (‒SH). Hydroxyethyl methylacrylate (HEMA) as functional monomer and dibenzoyl peroxide (BPO) as initiator were dissolved into 1,2-dichloroethane (DCE), and HEMA molecules are automatically combined around (S)-ibuprofen molecules by right of multi-site hydrogen bonds, forming self-assembly complex. A surface-initiating system of ‒SH/BPO was constituted at the interface between MPMS-SiO2 particles and DCE solution. The free radicals produced on the surfaces of MPMS-SiO2 particles initiated HEMA molecules around (S)-ibuprofen molecules to produce graft/crosslinking-polymerization on the surfaces of SiO2 particles. At the same time, (S)-ibuprofen molecules were wrapped in the cross-linked networks so that the surface-imprinting of (S)-ibuprofen was realized, forming (S)-ibuprofen surface imprinted particles ((S)-IBU-SIP). The enantiomeric recognition and resolution properties of (S)-IBU-SIP particles were investigated. The experimental results show that (S)-IBU-SIP particles have excellent enantiodiscrimination property and enantioseparation ability. The binding capacity of (S)-IBU-SIP particles for (S)-ibuprofen gets up to 177 mg g−1, and the selectivity coefficient of (S)-IBU-SIP particles for (S)-ibuprofen relative to (R)-ibuprofen is 5.03. For the ibuprofen raceme solution, after solid phase extraction by (S)-IBU-SIP particles, the optical purity (ee value of (S)-ibuprofen) of the eluent reaches up to 82.5%, whereas the optical purity (ee value of (R)-ibuprofen) of the supernatant is 44.2%.

CAS / MDL: 97-90-5
研究领域: 药物化学 · 分析化学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 17 · IF 1.86

The toughening behavior of PLLA and its asymmetric PLLA/PDLA blends with lower optical purity

Yanmei Guo,Jun Shao,Haoqing Hou

Linear poly( d -lactide) (PDLA) with various molecular weights is synthesized and incorporated into commercial poly( l -lactide) (PLLA) with different optical purities. And then, the crystallization, mechanical and thermal properties of the PLLA and PLLA/PDLA cast films are investigated. In the PLLA and PDLA/PLLA specimens with lower optical purity, few homochiral crystallites (HC) form in all the specimens and only a small amount of PLA stereocomplex crystallites (SC) are observed in the blends. The elongation at break of all the specimens is extraordinary high, >300%. Dynamic mechanical analyses indicate that the destruction temperature increases at first, and then depresses as enlarging the molecular weight of PDLA in these blends. For the PLLA and PLLA/PDLA with higher optical purity, more content of HC develops in neat PLLA, and both SC and HC produce in the PLLA/PDLA specimens. However, the strains of neat specimens and binary blends are much lower than that of specimens with lower optical purity. The specimens with higher optical purity exhibit higher destruction temperatures and lower loss factors. The high content of crystals (SC and HC) would act as the physical cross-linking points and provide a key factor to impede the deformation of neat PLLA and binary blends during stretching, which should result in the fragile behavior of the PLLA and PLLA/PDLA blends with higher optical purity. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44730.

CAS / MDL: 111-77-3
研究领域: 材料科学 · 高分子化学
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JOURNAL OF BIOTECHNOLOGY · 2019 · IF 3.163

Highly enantioselective resolution of racemic 1-phenyl-1,2-ethanediol to (S)-1-phenyl-1,2-ethanediol by Kurthia gibsonii SC0312 in a biphasic system

Fei Peng,Ying Zhao,Fang-Zhou Li,Xiao-Yang Ou,Ying-Jie Zeng,Min-Hua Zong,Wen-Yong Lou

The asymmetric resolution of racemic 1-phenyl-1,2-ethanediol (PED) to ( S )-PED by Kurthia gibsonii SC0312 ( K. gibsonii SC0312) was conducted in a biphasic system comprised of an organic solvent and aqueous phosphate buffer. The impacts of organic solvents on the whole cell catalytic activity, metabolic activity, membrane integrity, and material distribution were first evaluated. The results showed that all organic solvents, except for dibutyl phthalate, showed a detrimental effect on the metabolic activity of the cells, especially for those with low log P values. All organic solvents were capable of changing the membrane permeability and membrane integrity of the cells. Moreover, some organic solvents showed a good extraction of the oxidation product. Finally, a high yield of 47.7 % of ( S )-PED was obtained by the asymmetric resolution of racemic PED using K. gibsonii SC0312 in a biphasic system under the optimal conditions: racemic PED 120 mM, temperature 35 °C, reaction time 6 h, 180 rpm, and a volume ratio of dibutyl phthalate to aqueous phosphate buffer of 1:1. The optical purity of ( S )-PED increased from 51.3 % to >99 %. This work described an efficient approach to improve reaction efficiency, and constructed a highly effective biphasic reaction system for the fabrication of ( S )-PED via K. gibsonii SC0312.

研究领域: 生物化学 · 微生物学 · 有机合成
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APPLIED MICROBIOLOGY AND BIOTECHNOLOGY · 2013 ·Vol. 97 ·期 24 ·10329-10337 · IF 3.689

Highly enantioselective oxidation of phenyl methyl sulfide and its derivatives into optically pure (S)-sulfoxides with Rhodococcus sp. CCZU10-1 in an n-octane–water biphasic system

He Yu-Cai,Ma Cui-Luan,Yang Zhen-Xing,Zhou Min,Xing Zhen,Ma Jiang-Tao,Yu Hui-Lei

Enantiopure sulfoxides can be prepared via the asymmetric oxidation of sulfides using sulfide monooxygenases. The n -octane–water biphasic system was chosen for the bio-oxidation of a water-insoluble phenyl methyl sulfide (PMS) by Rhodococcus sp. CCZU10-1. In this n -octane–water system, the optimum reaction conditions were obtained. ( S )-phenyl methyl sulfoxide (( S )-PMSO) with >99.9 % enantiomeric excess formed at 55.3 mM in the n -octane–water biphasic system. Using fed-batch method, a total of 118 mM ( S )-PMSO accumulated in 1-L reaction mixture after the 7th feed, and no ( R )-PMSO and sulfone were detected. Moreover, Rhodococcus sp. CCZU10-1 displayed fairly good activity and enantioselectivity toward other sulfides. In conclusion, Rhodococcus sp. CCZU10-1 is a promising biocatalyst for synthesizing highly optically active sulfoxides.

CAS / MDL: 299-11-6
研究领域: 生物化学 · 微生物学 · 有机合成
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ORGANIC & BIOMOLECULAR CHEMISTRY · 2023 ·Vol. 21 ·期 16 ·3417-3422 · IF 3.2

Kinetic resolution of sulfoxides with high enantioselectivity using a new homologue of methionine sulfoxide reductase B

Yuyan Zhao,Xu Jiang,Shihuan Zhou,Jin Tian,Piao Yang,Yanli Chen,Quan Zhang,Xianlin Xu,Yongzheng Chen,Jiawei Yang

Optically pure sulfoxides are noteworthy compounds that find wide applications in various industrial fields. Here, we report a methionine sulfoxide reductase B (MsrB) homologue that exhibits high enantioselectivity and broad substrate scope for the kinetic resolution of racemic (rac) sulfoxides. This MsrB homologue, named liMsrB, was identified from Limnohabitans sp. 103DPR2 and showed good activity together with enantioselectivity towards a series of aromatic, heteroaromatic, alkyl and thioalkyl sulfoxides. Chiral sulfoxides in the S configuration were prepared in approximately 50% yield and 92–99% enantiomeric excess through kinetic resolution at an initial substrate concentration of up to 90 mM (11.2 g L−1). This study presents an efficient route for the enzymatic preparation of (S)-sulfoxides through kinetic resolution.

研究领域: 生物化学 · 酶工程 · 工业生物技术
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ADVANCED SYNTHESIS & CATALYSIS · 2016 ·Vol. 358 ·期 18 ·2923-2928 · IF 6.453

Efficient Biosynthesis of (R)- or (S)-2-Hydroxybutyrate from l-Threonine through a Synthetic Biology Approach

Peiyuan Yao,Yunfeng Cui,Shanshan Yu,Yuncheng Du,Jinhui Feng,Qiaqing Wu,Dunming Zhu

An efficient multi-enzyme cascade reaction for the synthesis of ( R )- or ( S )-2-hydroxybutyric acid [( R )- or ( S )-2-HB] from l -threonine was developed by using recombinant Escherichia coli cells expressing separately or co-expressing l -threonine deaminase from Escherichia coli K-12 ( ilvA ), formate dehydrogenase (FDH) from Candida boidinii and l -lactate dehydrogenase ( l -LDH) from Oryctolagus cuniculus or d -lactate dehydrogenase ( d -LDH) from Staphylococcus epidermidis ATCC 12228. Up to 750 mM of l -threonine were completely transformed to ( R )- or ( S )-2-HB in optically pure form (>99% ee ) with high isolated yields. This one-pot multi-enzyme transformation provides a new practical method for the synthesis of these important optically pure compounds.

CAS / MDL: 72-19-5
研究领域: 生物化学 · 合成生物学 · 代谢工程
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CHEMICAL RESEARCH IN CHINESE UNIVERSITIES · 2019 ·Vol. 35 ·期 5 ·792-798 · IF 1.071

Enantioselective Resolution of (±)-1-Phenylethyl Acetate by Using the Whole Cells of Deep-sea Bacterium Bacillus sp. DL-2

Dong Lu,Xu Yongkai,Zhang Yun,Sun Aijun,Hu Yunfeng

Bacillus sp. DL-2 was isolated from the deep sea of the Western Pacific and further utilized as novel biocatalysts to efficiently asymmetrically hydrolyze (±)-1-phenylethyl acetate. After the optimization of hydrolytic reactions, chiral chemicals ( R )-1-phenylethanol and ( S )-1-phenylethyl acetate were obtained with high optical purities (96% and 99.8%, respectively). Our research is about the asymmeric hydrolysis of (±)-1-phenylethyl acetate using whole-cell biocatalysts. In addition, the optical purity of ( S )-1-phenylethyl acetate generated through the kinetic resolution of (±)-1-phenylethyl acetate using the whole-cells of Bacillus sp. DL-2 was the highest report so far. Using the whole cells of deep sea bacterium Bacillus sp. DL-2 as the biocatalysts is an environmentally friendly method and will play critical roles in industrial asymmetric synthesis.

CAS / MDL: 112-40-3
研究领域: 生物化学 · 工业微生物学
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CHIRALITY · 2018 ·Vol. 30 ·期 6 ·769-776 · IF 1.833

Functional characterization of salt-tolerant microbial esterase WDEst17 and its use in the generation of optically pure ethyl (R)-3-hydroxybutyrate

Yilong Wang,Yongkai Xu,Yun Zhang,Aijun Sun,Yunfeng Hu

The two enantiomers of ethyl 3-hydroxybutyrate are important intermediates for the synthesis of a great variety of valuable chiral drugs. The preparation of chiral drug intermediates through kinetic resolution reactions catalyzed by esterases/lipases has been demonstrated to be an efficient and environmentally friendly method. We previously functionally characterized microbial esterase PHE21 and used PHE21 as a biocatalyst to generate optically pure ethyl ( S )-3-hydroxybutyrate. Herein, we also functionally characterized one novel salt-tolerant microbial esterase WDEst17 from the genome of Dactylosporangium aurantiacum subsp. Hamdenensis NRRL 18085. Esterase WDEst17 was further developed as an efficient biocatalyst to generate ( R )-3-hydroxybutyrate, an important chiral drug intermediate, with the enantiomeric excess being 99% and the conversion rate being 65.05%, respectively, after process optimization. Notably, the enantio-selectivity of esterase WDEst17 was opposite than that of esterase PHE21. The identification of esterases WDEst17 and PHE21 through genome mining of microorganisms provides useful biocatalysts for the preparation of valuable chiral drug intermediates.

CAS / MDL: 5405-41-4
研究领域: 生物化学 · 微生物学 · 药物合成
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