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2-脱氧-D-核糖
CHEMBIOCHEM · 2026 ·Vol. 27 ·期 14 ·e70476 · IF 2.8

Characterization of a Purine Nucleoside Phosphorylase From Colwellia sp. WH041 for Multienzyme Synthesis of Nucleoside Analogs

Shirong Wang,Yu Zhang,Fan Yang,Fuxue Chen,Xingcheng Shao,Gaofei Liu,Bin Wu

Multienzyme cascades provide an efficient biocatalytic strategy for synthesizing nucleoside analogs from simple sugar donors and nucleobases. In pentose‐to‐nucleoside cascades, purine nucleoside phosphorylase (PNP) catalyzes the terminal N‐glycosylation step and strongly influences product formation and substrate scope. Here, seven putative PNP homologs from microorganisms isolated from low‐temperature environments were evaluated under Ec RK‐ Ec PPM‐PNP cascade conditions. A PNP from Colwellia sp. WH041, designated Col PNP, showed the highest arabinofuranosylation activity and was selected for further characterization. Col PNP displayed optimal activity at 45 °C and exhibited a 12.7‐fold higher catalytic efficiency than Escherichia coli PNP at the same temperature. Molecular dynamics simulations supported the favorable catalytic performance of Col PNP under moderate‐temperature conditions. After optimization of the Ec RK‐ Ec PPM‐ Col PNP cascade, vidarabine conversion reached 58.2% within 12 h. The optimized system was further applied to synthesize diverse nucleoside analogs with conversions of 45.8%–89.8%, and guanosine analogs were obtained through sequential Ec ADA‐mediated deamination. This study expands the PNP toolbox and demonstrates Col PNP as an efficient module for enzymatic nucleoside analog synthesis. A purine nucleoside phosphorylase from Colwellia sp. WH041, Col PNP, is identified as an efficient module for pentose‐to‐purine nucleoside synthesis. Integrated with Ec RK and Ec PPM, Col PNP enables direct conversion of unprotected D‐pentoses and purine bases into diverse nucleoside analogs with up to 89.9% conversion.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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ChemSusChem · 2023 ·Vol. 16 ·期 12 ·e202300208 · IF 8.4

Synthesis and Computational Investigation of Antioxidants Prepared by Oxidative Depolymerization of Lignin and Aldol Condensation of Aromatic Aldehydes

Daihong Gao,Denghao Ouyang,Yuchen Bai,Xuebing Zhao

Graphical New antioxidants were prepared by oxidative depolymerization of lignin followed by aldol condensation to form conjugated structure with benzene ring. Kinetics of aldol condensation between lignin-derived aromatic aldehydes and methyl ethyl ketone was investigated. The increase in the antioxidation ability was confirmed by experimentation and interpreted by density functional theoretical calculation. Novel antioxidants are synthesized by CuSO 4 -catalyzed oxidative depolymerization of lignin to form aromatic aldehydes followed by aldol condensation with methyl ethyl ketone (MEK). Aldol condensation greatly improves the antioxidation ability of lignin depolymerized products. Three lignin monomeric aromatic aldehydes, – p -hydroxybenzaldehyde, vanillin, and syringaldehyde – are further employed for aldol condensation with MEK, resulting in successful synthesis of new antioxidants 1-(4-hydroxyphenyl)pent-1-en-3-one (HPPEO), 1-(4-hydroxy-3-methoxyphenyl)pent-1-en-3-one (HMPPEO), and 1-(4-hydroxy-3,5-dimethoxyphenyl)pent-1-en-3-one (HDMPPEO), respectively. Kinetic modeling illustrates that p -hydroxybenzaldehyde has the highest rate of reaction with MEK, followed by vanillin and then syringaldehyde, which is probably affected by the presence of methoxy groups. The syringaldehyde-derived product (HDMPPEO) displays the best antioxidation ability. As revealed by density functional theory calculations, electron-donating groups, such as methoxy, and conjugated side chains effectively improve the antioxidation ability. A hydrogen atom transfer (HAT) mechanism tends to occur in nonpolar solvents, whereas a sequential proton-loss electron transfer (SPLET) mechanism is favored in polar solvents. This work thus can inspire new pathways for valorization of lignin to produce high value-added products.

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JOURNAL OF MOLECULAR LIQUIDS · 2023 · IF 6

Luminescent lanthanide metallogel as a sensor array to efficiently discriminate various saccharides

Binbin Zhang,Jiao Ma,Kaide Ou,Xin Cong,Hao Zou,Yonggui Liao,Yajiang Yang,Hong Wang

By loading 3-nitrophenylboronic acid (3-NPBA) which can react with saccharide, the fluorescence lanthanide metallogel can emit fluorescence signals at 398, 490 and 546 nm. Thus, a three-dimensional responsive fluorescence sensor array (H 6 L/Tb 3+ /3-NPBA) was prepared to recognize saccharides. Due to the typical pH responsiveness of the fluorescence behavior of the sensor array, it is suitable for H + generation systems, such as the reaction of 3-NPBA with cis -diol of saccharides. The response of fluorescence signal intensity to 15 different saccharides was measured, and the qualitative discrimination of those saccharides was investigated by principal component analysis (PCA). The results showed that PCA elliptic clusters did not overlap, even though the concentration of the saccharides was as low as 3 mmol/L, and the discrimination rate of each saccharide reached 100 %. The “double blind” experiment indicated that the sensor system has good ability to discriminate unknown component samples. Furthermore, the discrimination rate of fructose/glucose mixtures with varied mole ratios also reached 100 %. The method of Euclidean distance confirmed that there was a good linear correlation between PCA elliptic clusters of fructose and its concentration, which could realize the quantitative analysis of fructose. The results of PCA indicated that the elliptic clusters of tea drinks with various sugars and commercially available sugar-containing drinks were loosely distributed, which further confirmed that the sensor system can effectively discriminate the saccharides under the interference of complex components.

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INORGANICA CHIMICA ACTA · 2022 · IF 3.118

A multifunctional and water-stable Cd (II) coordination polymer: Sensitive detection of roxarsone, Fe3+, CrO42− and Cr2O72− in aqueous media

Zong-Ying Li,Hong-Xia Zhang,Tian-Sheng He,Hong-Xin Jiang,Xiao-Wei Liu,Li-Na Zhu,Xiao-Zeng Li,De-Ming Kong

A two-dimensional (2D) water-stable Cd (II) luminescent coordination polymer ( 1 ), namely {[CdLCl 2 ]} n , was obtained through assembly of a new 2-deoxy- d -ribose derivative ligand (L) with CdCl 2 , 1 showed high stability in water. Further investigation showed that 1 can be used as luminescent probe for the organoarsenic compound Roxarsine (ROX) with high selectivity and sensitivity, high quenching constants (K SV  = 2.34 × 10 4 M −1 ), low limits of detection (LOD) (0.16 μM) and good recyclability in aqueous media. In addition, this luminescent probe can detect some inorganic harmful ions (Fe 3+ , Cr 2 O 7 2− and CrO 4 2− ) with excellent versatility. The detection mechanism was proved that the quenching was caused by competitive absorption and resonance energy transfer effect between 1 and analytes. More strikingly, a simple 1 -based test strip was developed owing to the quick response and recyclability of 1 , which shows visible quenching signals under UV light even when analytes concentrations are as low as 5 μM. This work has provided an effective method for the design of multifunctional CP luminescent sensors for pollutants detections in aqueous media.

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Biomass Conversion and Biorefinery · 2019 ·Vol. 10 ·期 2 ·277-287 · IF 2.326

Formation of humins during degradation of carbohydrates and furfural derivatives in various solvents

Shi Ning,Liu Qiying,Cen Hu,Ju Rongmei,He Xiong,Ma Longlong

Humins are undesired solids formed during the hydrothermal degradation of carbohydrates. In order to reveal the mechanism of formation of humins, we studied the degradation behavior of 11 model compounds including carbohydrates and furfural derivatives, within water and various pure organic solvents as reaction media. All the studied carbohydrates could generate solid humins in both water and studied organic solvents except ethanol, while the furfural derivatives could generate solid humins in only water. The results could be explained by regarding the formed α-carbonyl aldehydes and α,β-unsaturated aldehydes as primary precursors for formation of humins. Furfural derivatives could generate chain α-carbonyl aldehydes (for example, 6-hydroxy-2,5-dioxohexanal from 5-hydroxymethylfurfural and 2-oxopentanedial from furfural) through hydrolytic ring opening reaction; thus, water is essential for these furfural derivatives to generate humins. As for carbohydrates, they could generate α-carbonyl aldehydes and α,β-unsaturated aldehydes through simple step of β-elimination in all solvents; thus, they could form humins in both water and studied organic solvents except ethanol. Ethanol could react with α-carbonyl aldehydes by acetalization; thus, the condensation between α-carbonyl aldehydes was suppressed in ethanol, leading to few humins formation from carbohydrates. Based on the above analysis, we proposed that the formed α-carbonyl aldehydes and α,β-unsaturated aldehydes should be the primary precursor of humins.

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INDUSTRIAL CROPS AND PRODUCTS · 2015 · IF 2.837

Comparative analyses of flavonoids compositions and antioxidant activities of Hawk tea from six botanical origins

Li-Hong Tan,Dan Zhang,Gang Wang,Bao Yu,Sheng-Ping Zhao,Jian-Wei Wang,Ling Yao,Wei-Guo Cao

The aim of this study was to compare the flavonoids compositions, content and antioxidant activities of Hawk tea from six botanical origins for screening the most suitable botanical origins. The main flavonoids of Hawk teas from Litsea coreana Levl. var. lanuginose were identified, and six high contents of individual flavonoids (hyperin, isoquercitrin, quercitrin, astragalin, quercetin and kaempferol) were quantitative and comparative analysis. Moreover the potential antioxidant capacity of Hawk tea was measured by using in vitro antioxidant assays. The above experimental data were all used for the principal component analysis. The statistical results showed that the extracts from Machilus chuanchienensis S. Lee and L. coreana Levl. var. lanuginose appeared closely positioned in the positive regions, indicated the higher flavonoids and antioxidant activity compared with other species. Thus, they were temporarily considered as good sources of Hawk tea.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2013 · IF 2.596

Effect of different drying methods on chemical composition and bioactivity of tea polysaccharides

Yuanfeng Wang,Yangyang Liu,Jianglei Huo,Tingtong Zhao,Jian Ren,Xinlin Wei

Four polysaccharides (TPS-F, TPS-V, TPS-S and TPS-M) were obtained from tea ( Camellia sinensis ) leaves by freeze-drying, vacuum-drying, spray-drying and microwave-vacuum drying, respectively. Their chemical composition and biological properties were comparatively studied. The results showed these TPS were similar in IR, UV absorption and distribution of molecular weight. However, they showed significant differences ( P   <   0.05) in yields of crude polysaccharides and contents of protein and total polyphenols. Furthermore, morphological analysis showed their surface differed from each other in size and shape when viewed by SEM, from which surface of TPS-F was rough and porous, surface of TPS-S was evenly particles, and surfaces of the other two were similar to anomalistic bricks. In addition, the bioactivity of them was also evaluated. It was found TPS-F exhibited relatively better ability on metal chelating and superoxide radicals scavenging assays than others, and TPS-V exhibited higher ability on α-glycosidase and α-amylase inhibition assays than others with inhibitory percentages of 82.75% and 92.8%.

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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Hollow mesoporous Prussian blue nanoenzymes as Rapamycin carrier for targeted treatment of ischemia/reperfusion-induced acute kidney injury through pro-mitophagy and oxidative stress alleviation

Yanhui Wang,Huayu Fu,Bangqi Huang,Ziyang Liang,Yijun Shen,Yulan Wang,Jun Wu,Yi Zhao

The kidney’s abundant mitochondrial content and substantial oxygen requirements make it particularly vulnerable to a series of detrimental events following ischemia/reperfusion (I/R). These events encompass oxidative stress, mitochondrial impairment, depletion of adenosine triphosphate (ATP), and inflammation, cumulatively leading to acute kidney injury (AKI). Currently, no approved therapy beyond supportive care is available for AKI. While numerous studies have focused on neutralizing pre-existing reactive oxygen species (ROS) to mitigate AKI, insufficient attention has been paid to addressing the root causes of ROS. Here, we prepared Rapamycin (Rapa)-loaded hollow mesoporous Prussian blue nanoparticles (HMPB-Rapa) and grafted injured renal-targeted hyaluronic acid (HA) onto HMPB-Rapa (HA-HMPB-Rapa), which effectively scavenge pre-existing ROS and the source (massive damaged mitochondria) through the dual function of HMPB carrier and Rapa, thus preventing the further burst of ROS. In the I/R-induced AKI rat model, a single-dose of HA-HMPB-Rapa 6 h after I/R injury effectively inhibited oxidative stress and inflammation, protected renal cells from apoptotic damage, as well as ultimately restored renal function, and attenuated pathological changes. Mechanistically, HA-HMPB-Rapa cleared damaged mitochondria by activating the pro-mitophagy signaling pathway (PINK-1/Parkin-P62-LC3), cutting off the conduction in the intrinsic apoptotic pathway mediated by the Bax-Cyt-c-Cleaved Casp-3 signaling axis, and reduced the expression of renal tubular marker kidney injury molecule-1. HA-HMPB-Rapa represents an exciting new avenue for the treatment of diseases related to I/R-induced injury.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2012 · IF 2.453

Antioxidant activities potential of tea polysaccharide fractions obtained by ultra filtration

Yuanfeng Wang,Zhiwei Yang,Xinlin Wei

Three polysaccharide fractions (TPS1, TPS2 and TPS3) with different molecular weights were obtained using ultra filtration membranes from crude tea polysaccharide (CTPS) extracted from abandoned lower grade tea leaves. Each fraction contained different contents of neutral sugar, uronic acid, protein, and total polyphenols. These differences provided basis for the antioxidant and free radical scavenging activity of these polysaccharide fractions. The molecular weights of TPS1, TPS2, and TPS3 were around 2.40   ×   10 5   Da, 2.14   ×   10 4   Da, and 2.46   ×   10 3   Da, respectively. In general, TPS1 and CTPS had stronger antioxidant activity, TPS2 and TPS3 had lower antioxidant activity. TPS1 had higher activity for DPPH and lipid per oxidation inhibition. But it had lower capacity for reducing power and metal chelating. This might be due to its higher content of hexuronic acid and larger molecular weight. The order of inhibition activity of lipid per oxidation of various polysaccharide fractions was the same as DPPH radical scavenging activity, as well as the order of metal chelating activity of various polysaccharide fractions similar to hydroxyl radical scavenging activity, which demonstrated that hydroxyl radical scavenging activity of polysaccharide relied heavily on the Fe 2+ metal chelating to decrease the generation of hydroxyl radical.

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FIBERS AND POLYMERS · 2024 ·Vol. 25 ·期 7 ·2669-2682 · IF 2.2

A Novel Cotton Scouring Using Pectinase in Combination with Fenton System

Luo Laipeng,Ding Chenkun,Zhu Qinting,Liu Lei,Wang Ping,Wang Qiang,Yu Yuanyuan

Untreated natural cotton fabrics are hydrophobic due to the high content of pectin and waxes, and the fabrics need to improve the wettability by scouring for the demands of the subsequent processing such as dyeing and finishing. In this study, a new scouring method for cotton fabrics was developed by pectin hydrolase combined with Fenton system (Fe 2+ /H 2 O 2 ). The mechanism of pectin degradation by pectinase combined with Fe 2+ /H 2 O 2 was investigated. The results showed that α-1,4-glycosidic bonds of water-soluble pectin could be degraded more efficiently by pectinase hydrolysis and Fe 2+ /H 2 O 2 oxidation. The fabrics scoured with pectinase → Fe 2+ /H 2 O 2 had less wetting time (4.25 s) and higher vertical wicking height (9.80 cm) compared to the fabrics treated with pectinase alone (> 120 s, 5.15 cm). The results of bleaching and dyeing experiments indicated that the whiteness and dyeing properties of the fabrics were not negatively affected by pectinase → Fe 2+ /H 2 O 2 treatment, and the strength loss of the fabrics (11.79%) was lower than that of the fabrics with conventional NaOH treatment (20.16%). The results of the experiments in the pilot-scale machine showed that various performance indicators of the fabrics scoured by pectinase → Fe 2+ /H 2 O 2 reached the level of the conventional NaOH treatment, which demonstrated the possibility for practical application of pectinase → Fe 2+ /H 2 O 2 scouring. The cotton fabric scouring using pectinase → Fe 2+ /H 2 O 2 is an effective and feasible new method with advantages such as environmental friendliness, mild treatment conditions, and good treatment effect.

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Food Bioscience · 2024 · IF 4.8

Protein glycosylation inhibitory effects and mechanisms of phloretin and phlorizin

Yushi Wei,Jianmei Wu,Xi Peng,Xing Hu,Deming Gong,Guowen Zhang

The anti-glycation potential and mechanism of phloretin and phlorizin were investigated in the study. In the methylglyoxal (MGO)-human serum albumin (HSA) glycosylation system, the inhibition against fluorescent advanced glycosylation end products (AGEs) was more than 60% at 960 μM phloretin and phlorizin. They decreased carbonylation and oxidative damage of protein, protected thiol groups and secondary structure of protein and inhibited protein aggregates. Treated with 1.37 mM phloretin or phlorizin, O 2 − · scavenging was more than 80%, and 1 mM phloretin or phlorizin chelated 60.08% or 28.11% of Fe 2+ , respectively. Analysis of HPLC and LC-QqQ-MS shown phloretin captured MGO by forming adducts with MGO, with capture rates of 92.67% within 24 h. The capture rate of phlorizin to MGO was 56.40%. The anti-glycosylation mechanisms of them could include the structural protection of HSA, capture of MGO, O 2 − · and ·OH scavenging and chelation of Fe 2+ . These findings may provide a theoretical basis for the application of phloretin and phlorizin as novel anti-glycosylation agents.

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JOURNAL OF CONTROLLED RELEASE · 2025 · IF 11.5

Tannic acid‑cerium nanoenzymes serve as broad-spectrum antioxidants to alleviate acute kidney injury by modulating macrophage polarization, mitophagy and endoplasmic reticulum stress

Huayu Fu,Yanhui Wang,Bangqi Huang,Zonghao Liang,Yumin Li,Zhong Cao,Jun Wu,Yi Zhao

Acute kidney injury (AKI) is a critical condition marked by a rapid decline in renal function, primarily driven by oxidative stress, mitochondrial dysfunction, and inflammation. Despite extensive research, effective therapeutic strategies addressing the complex pathophysiology of AKI remain limited. In this study, we prepared a tannic acid‑cerium nanoenzyme (TA-Ce) and explored its potential for treating AKI. TA-Ce, synthesized via a one-pot method, demonstrated strong reactive oxygen species (ROS) scavenging, therapeutic efficacy, and biocompatibility in vitro and in vivo . TA-Ce, approximately 25.6 nm in size, was obtained by optimizing the molar ratios of TA to Ce and pH conditions, resulting in effective accumulation in the injured kidney. In addition, TA-Ce exhibited broad-spectrum antioxidant ability, capable of scavenging various ROS and alleviating oxidative stress. Notably, TA-Ce outperformed the conventional anti-inflammatory drug N -acetylcysteine (NAC) in both rhabdomyolysis-induced AKI (RM-AKI) and cisplatin-induced AKI (CP-AKI) mouse models. Mechanistic studies in RM-AKI revealed that TA-Ce disrupted the vicious cycle of oxidative stress, mitochondrial damage, endoplasmic reticulum stress, apoptosis, and inflammation. The nanoenzyme restored mitochondrial autophagic flux by inhibiting the P62-LC3 signaling pathway and alleviated endoplasmic reticulum stress by suppressing the IRE1-XBP1s pathway. Consequently, this prevented the downstream activation of the Bcl-2-Bax-Cyt-c-Cleaved Casp-3 apoptotic pathway and the NF-κB inflammatory pathway, ultimately ameliorating RM-AKI. This study lays a strong foundation for the development of metal-polyphenol nanomaterials as a therapeutic strategy for clinical AKI.

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