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Bacterial nanocellulose: A versatile biopolymer production using a cost-effective wooden disc based rotary reactor 细菌纳米纤维素:利用经济高效的木盘式旋转反应器生产多功能生物聚合物。
IF 3.2 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-25 DOI: 10.1002/bip.23577
Ashish Jagtap, Syed G. Dastager

Bacterial nanocellulose (BNC) has various unique qualities, including high mechanical strength, crystallinity, and high water-holding capacity, which makes it appropriate for a wide range of industrial applications. But its lower yield coupled with its high production cost creates a barrier to its usage. In this study, we have demonstrated the better yield of BNC from an indigenous strain Komagataeibacter rhaeticus MCC-0157 using a rotary disc bioreactor (RDB) having a wooden disc. The RDB was optimized based on the type of disc material, distance between the disc, and rotation speed to get the highest yield of 13.0 g/L dry material using Hestrin–Schramm (H–S) medium. Further, the bioreactor was compared for the BNC production using reported medium, which is used for static condition; the RDB showed up to fivefold increase in comparison with the static condition reported. Komagataeibacter rhaeticus MCC-0157 was previously reported to be one of the highest BNC producing stains, with 8.37 g/L of dry yield in static condition in 15 days incubation. The designed RDB demonstrated 13.0 g/L dry yield of BNC in just 5 days. Other characteristics of BNC remain same as compared with static BNC production, although the difference in the crystallinity index was observed in RDB (84.44%) in comparison with static (89.74%). For the first time, wooden disc was used for rotary bioreactor approach, which demonstrated higher yield of BNC in lesser time and can be further used for sustainable production of BNC at the industrial level.

细菌纳米纤维素(BNC)具有高机械强度、结晶性和高保水能力等各种独特品质,因此适合广泛的工业应用。但其较低的产量和较高的生产成本阻碍了它的应用。在本研究中,我们利用木质圆盘旋转盘生物反应器(RDB)从本地菌株 Komagataeibacter rhaeticus MCC-0157 中获得了较高的 BNC 产量。根据圆盘材料类型、圆盘间距离和旋转速度对 RDB 进行了优化,使用 Hestrin-Schramm (H-S) 培养基获得了 13.0 克/升的最高干物质产量。此外,该生物反应器还与用于静态条件的报告培养基的 BNC 产量进行了比较;与报告的静态条件相比,RDB 的产量增加了五倍。据报道,Komagataeibacter rhaeticus MCC-0157 是 BNC 产量最高的菌种之一,在静态条件下培养 15 天,干产量为 8.37 克/升。设计的 RDB 仅在 5 天内就显示出 13.0 克/升的 BNC 干产量。与静态 BNC 生产相比,BNC 的其他特征保持不变,但在 RDB 中观察到结晶度指数(84.44%)与静态(89.74%)不同。木盘首次用于旋转生物反应器方法,在较短时间内获得了较高的 BNC 产量,可进一步用于工业级 BNC 的可持续生产。
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引用次数: 0
Ewing Sarcoma Related protein 1 recognizes R-loops by binding DNA forks 尤文肉瘤相关蛋白 1 通过结合 DNA 叉来识别 R 环。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-21 DOI: 10.1002/bip.23576
Michelle A. Lay, Valery F. Thompson, Ajibola D. Adelakun, Jacob C. Schwartz

EWSR1 (Ewing Sarcoma Related protein 1) is an RNA binding protein that is ubiquitously expressed across cell lines and involved in multiple parts of RNA processing, such as transcription, splicing, and mRNA transport. EWSR1 has also been implicated in cellular mechanisms to control formation of R-loops, a three-stranded nucleic acid structure consisting of a DNA:RNA hybrid and a displaced single-stranded DNA strand. Unscheduled R-loops result in genomic and transcription stress. Loss of function of EWSR1 functions commonly found in Ewing Sarcoma correlates with high abundance of R-loops. In this study, we investigated the mechanism for EWSR1 to recognize an R-loop structure specifically. Using electrophoretic mobility shift assays (EMSA), we detected the high affinity binding of EWSR1 to substrates representing components found in R-loops. EWSR1 specificity could be isolated to the DNA fork region, which transitions between double- and single-stranded DNA. Our data suggests that the Zinc-finger domain (ZnF) with flanking arginine and glycine rich (RGG) domains provide high affinity binding, while the RNA recognition motif (RRM) with its RGG domains offer improved specificity. This model offers a rational for EWSR1 specificity to encompass a wide range in contexts due to the DNA forks always found with R-loops.

EWSR1(尤文肉瘤相关蛋白 1)是一种 RNA 结合蛋白,在细胞系中普遍表达,参与 RNA 处理的多个环节,如转录、剪接和 mRNA 运输。EWSR1 还与控制 R 环形成的细胞机制有关,R 环是一种三链核酸结构,由 DNA:RNA 杂交和移位的单链 DNA 链组成。计划外的 R 环会导致基因组和转录压力。尤文肉瘤中常见的 EWSR1 功能缺失与 R 环的高丰度相关。在这项研究中,我们研究了 EWSR1 特异性识别 R 环结构的机制。通过电泳迁移试验(EMSA),我们检测到 EWSR1 与代表 R 环成分的底物有高亲和力结合。EWSR1 的特异性可被分离到 DNA 叉区,该区域在双链和单链 DNA 之间转换。我们的数据表明,锌指结构域(ZnF)及其侧翼富含精氨酸和甘氨酸的结构域(RGG)提供了高亲和力的结合,而 RNA 识别基序(RRM)及其 RGG 结构域则提供了更好的特异性。这个模型为 EWSR1 的特异性提供了一个合理的解释,由于 DNA 叉总是与 R 环一起出现,因此 EWSR1 的特异性涵盖了广泛的情况。
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引用次数: 0
Application of hydrogel microneedles in the oral cavity 水凝胶微针在口腔中的应用。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-20 DOI: 10.1002/bip.23573
Yiyao He, Dawei He, Lin Fan, Song Ren, Lin Wang, Jiang Sun

Microneedles are a transdermal drug delivery system in which the needle punctures the epithelium to deliver the drug directly to deep tissues, thus avoiding the influence of the first-pass effect of the gastrointestinal tract and minimizing the likelihood of pain induction. Hydrogel microneedles are microneedles prepared from hydrogels that have good biocompatibility, controllable mechanical properties, and controllable drug release and can be modified to achieve environmental control of drug release in vivo. The large epithelial tissue in the oral cavity is an ideal site for drug delivery via microneedles. Hydrogel microneedles can overcome mucosal hindrances to delivering drugs to deep tissues; this prevents humidity and a highly dynamic environment in the oral cavity from influencing the efficacy of the drugs and enables them to obtain better therapeutic effects. This article analyzes the materials and advantages of common hydrogel microneedles and reviews the application of hydrogel microneedles in the oral cavity.

微针是一种透皮给药系统,针头刺破上皮细胞,将药物直接输送到深层组织,从而避免了胃肠道首过效应的影响,并将诱发疼痛的可能性降至最低。水凝胶微针是由水凝胶制备的微针,具有良好的生物相容性、可控的机械性能和可控的药物释放,并可通过改性实现体内药物释放的环境控制。口腔的上皮组织较大,是通过微针给药的理想场所。水凝胶微针可以克服粘膜障碍,将药物输送到深层组织;这样可以防止口腔中的湿度和高动态环境对药物疗效的影响,使药物获得更好的治疗效果。本文分析了常见水凝胶微针的材料和优势,并综述了水凝胶微针在口腔中的应用。
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引用次数: 0
In vitro and in vivo investigation of Argiope bruennichi spider silk-based novel biomaterial for medical use Argiope bruennichi 蜘蛛丝新型医用生物材料的体外和体内研究。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-16 DOI: 10.1002/bip.23572
Seçil Karahisar Turan, Aysun Kılıç Süloğlu, Semra İde, Tuncay Türkeş, Nurhayat Barlas

As a natural and biocompatible material with high strength and flexibility, spider silk is frequently used in biomedical studies. In this study, the availability of Argiope bruennichi spider silk as a surgical suture material was investigated. The effects of spider silk-based and commercial sutures, with and without Aloe vera coating, on wound healing were evaluated by a rat dorsal skin flap model, postoperatively (7th and 14th days). Biochemical, hematological, histological, immunohistochemical, small angle x-ray scattering (SAXS) analyses and mechanical tests were performed. A. bruennichi silk did not show any cytotoxic effect on the L929 cell line according to MTT and LDH assays, in vitro. The silk materials did not cause any allergic reaction, infection, or systemic effect in rats according to hematological and biochemical analyses. A. bruennichi spider silk group showed a similar healing response to commercial sutures. SAXS analysis showed that the 14th-day applications of A. bruennichi spider silk and A. vera coated commercial suture groups have comparable structural results with control group. In conclusion, A. bruennichi spider silk is biocompatible in line with the parameters examined and shows a healing response similar to the commercial sutures commonly used in the skin.

蜘蛛丝是一种天然的生物相容性材料,具有高强度和柔韧性,经常被用于生物医学研究。本研究调查了 Argiope bruennichi 蜘蛛丝作为手术缝合材料的可用性。通过大鼠背侧皮瓣模型,评估了术后(第 7 天和第 14 天)涂有或未涂芦荟的蜘蛛丝缝合线和商用缝合线对伤口愈合的影响。对其进行了生化、血液学、组织学、免疫组化、小角 X 射线散射(SAXS)分析和机械测试。根据 MTT 和 LDH 试验,青蒿素丝在体外对 L929 细胞株没有任何细胞毒性作用。根据血液学和生化分析,蛛丝材料不会对大鼠造成任何过敏反应、感染或全身影响。A. bruennichi 蜘蛛丝组显示出与商业缝合线相似的愈合反应。SAXS 分析表明,应用第 14 天的 A. bruennichi 蜘蛛丝组和 A. vera 包覆商业缝合线组与对照组的结构结果相当。总之,A. bruennichi 蜘蛛丝的生物相容性符合所检测的参数,其愈合反应与皮肤常用的商业缝合线相似。
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引用次数: 0
Efficient heterogeneous synthesis of nucleophilic carboxymethyl hydrazides of polysaccharides 多糖亲核羧甲基酰肼的高效异构合成。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-12 DOI: 10.1002/bip.23574
Hendryk Würfel, Annett Pfeifer, Thomas Heinze

Nucleophilic moieties in polysaccharides (PS) with distinct higher reactivity compared with the hydroxy group are interesting for sustainable applications in chemistry, medicine, and pharmacy. An efficient heterogeneous method for the formation of such nucleophilic PS is described. Employing alcohols as slurry medium, protonated carboxymethyl (CM) PS and hydrazine hydrate are allowed to react at elevated temperatures. The CM derivatives of starch and pullulan can be transformed almost quantitatively to the corresponding hydrazides. The reaction is less efficient for CM dextrans and CM xylans. As slurry media, 2-propanol and ethanol were probed, and the results are compared with a homogeneous procedure performed in water. Overall, the heterogeneous procedure is superior compared with the homogeneous route. 2-Propanol is the best slurry medium investigated yielding PS hydrazides with the highest nitrogen content.

与羟基相比,多糖(PS)中的亲核分子具有更高的反应活性,可持续应用于化学、医学和药学领域。本文介绍了一种形成此类亲核多糖的高效异构方法。使用醇类作为淤浆介质,质子化的羧甲基(CM)PS 和水合肼在高温下发生反应。淀粉和拉普兰的 CM 衍生物几乎可以定量地转化为相应的酰肼。对于 CM 右旋糖酐和 CM 木聚糖来说,该反应的效率较低。研究人员将 2-丙醇和乙醇作为浆料介质,并将结果与在水中进行的均相反应进行了比较。总体而言,异构过程优于均相过程。2 丙醇是所研究的最佳淤浆介质,可产生含氮量最高的 PS 联酰肼。
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引用次数: 0
Exploring helix structures of γ-peptides based on 2-(aminomethyl)cyclopentanecarboxylic acid 探索基于 2-(氨基甲基)环戊烷羧酸的 γ 肽的螺旋结构。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-03-11 DOI: 10.1002/bip.23575
Hae Sook Park, Joo Yun Lee, Young Kee Kang

Conformational search and density functional theory calculations were performed to explore the preferences of helical structures for chiro-specific oligo-γ-peptides of 2-(aminomethyl)cyclopentanecarboxylic acid (γAmc5) with a cyclopentyl constraint on the Cα–Cβ bond in solution. The dimer and tetramer of γAmc5 (1) with homochiral (1S, 2S) configurations exhibited a strong preference for the 9-membered helix foldamer in solution, except for the tetramer in water. However, the oligomers of γAmc5 (1) longer than tetramer preferentially adopted a right-handed (P)-2.614-helix (H1-14) as the peptide sequence becomes longer and as solvent polarity increases. The high stabilities for H1-14 foldamers of γAmc5 (1) in solution were ascribed to the favored solvation free energies. The calculated mean backbone torsion angles for H1-14 helix foldamers of γAmc5 (1) were similar to those calculated for oligomers of other γ-residues with cyclopentane or cyclohexane rings. However, the substitution of cyclopentane constraints on the Cα−Cβ bond of the γAmc5 (1) residue resulted in different conformational preferences and/or handedness of helix foldamers. In particular, the pyrrolidine-substituted analogs of the H1-14 foldamers of γAmc5 (1) with adjacent amine diads substituted at a proximal distance are expected to be potential catalysts for the crossed aldol condensation in nonpolar and polar solvents.

研究人员通过构象搜索和密度泛函理论计算,探索了溶液中 Cα -Cβ 键受环戊基约束的 2-(氨甲基)环戊烷羧酸(γAmc5)的螺旋结构对 chiro 特异性寡-γ-肽的偏好。具有同手性(1S、2S)构型的 γAmc5 (1) 二聚体和四聚体在溶液中表现出强烈的 9 元螺旋折叠体偏好,但水中的四聚体除外。然而,随着肽序列的变长和溶剂极性的增加,长于四聚体的γAmc5 (1) 寡聚体更倾向于采用右手(P)-2.614 -螺旋(H1 -14)。γAmc5 (1) 的 H1 -14 折叠体在溶液中的高稳定性归因于溶解自由能。计算得出的 γAmc5 (1) H1 -14 螺旋折叠体的平均骨干扭转角与计算得出的其他具有环戊烷或环己烷环的γ-残基的低聚物的扭转角相似。然而,环戊烷对γAmc5 (1) 残基的 Cα -Cβ 键的限制替代导致了不同的构象偏好和/或螺旋折叠体的手性。特别是,γAmc5 (1) 的 H1 -14 折叠体的吡咯烷取代类似物与相邻的二元胺在近端距离上被取代,有望成为在非极性和极性溶剂中进行交叉醛醇缩合的潜在催化剂。
{"title":"Exploring helix structures of γ-peptides based on 2-(aminomethyl)cyclopentanecarboxylic acid","authors":"Hae Sook Park,&nbsp;Joo Yun Lee,&nbsp;Young Kee Kang","doi":"10.1002/bip.23575","DOIUrl":"10.1002/bip.23575","url":null,"abstract":"<p>Conformational search and density functional theory calculations were performed to explore the preferences of helical structures for chiro-specific oligo-γ-peptides of 2-(aminomethyl)cyclopentanecarboxylic acid (γAmc<sub>5</sub>) with a cyclopentyl constraint on the C<sup>α</sup>–C<sup>β</sup> bond in solution. The dimer and tetramer of γAmc<sub>5</sub> (<b>1</b>) with homochiral (1<i>S</i>, 2<i>S</i>) configurations exhibited a strong preference for the 9-membered helix foldamer in solution, except for the tetramer in water. However, the oligomers of γAmc<sub>5</sub> (<b>1</b>) longer than tetramer preferentially adopted a right-handed (<i>P</i>)-2.6<sub>14</sub>-helix (H<sub>1</sub>-14) as the peptide sequence becomes longer and as solvent polarity increases. The high stabilities for H<sub>1</sub>-14 foldamers of γAmc<sub>5</sub> (<b>1</b>) in solution were ascribed to the favored solvation free energies. The calculated mean backbone torsion angles for H<sub>1</sub>-14 helix foldamers of γAmc<sub>5</sub> (<b>1</b>) were similar to those calculated for oligomers of other γ-residues with cyclopentane or cyclohexane rings. However, the substitution of cyclopentane constraints on the C<sup>α</sup>−C<sup>β</sup> bond of the γAmc<sub>5</sub> (<b>1</b>) residue resulted in different conformational preferences and/or handedness of helix foldamers. In particular, the pyrrolidine-substituted analogs of the H<sub>1</sub>-14 foldamers of γAmc<sub>5</sub> (<b>1</b>) with adjacent amine diads substituted at a proximal distance are expected to be potential catalysts for the crossed aldol condensation in nonpolar and polar solvents.</p>","PeriodicalId":8866,"journal":{"name":"Biopolymers","volume":"115 3","pages":""},"PeriodicalIF":2.9,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/bip.23575","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140093343","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correlation between the activation energy of PLA respectively PLA/starch composites and mechanical properties with regard to differ accelerated aging conditions 聚乳酸/淀粉复合材料的活化能分别与不同加速老化条件下的机械性能之间的相关性。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-02-22 DOI: 10.1002/bip.23571
Margarita Reit, Jan-Christoph Zarges, Hans-Peter Heim

Within this research semi-crystalline polylactide and composites with 50 wt.% native potato starch were compounded and injection molded. The material was mechanically characterized by tensile, three-point bending, and Charpy impact tests. These tests were carried out in the freshly molded state and after 332 and 792 h of storage at accelerated temperature or humidity. The respective activation energy was calculated by applying the Flynn-Wall-Ozawa method. The focus of the study was to investigate the correlation between the activation energy and the related mechanical and thermal properties. The results showed that the addition of native potato starch as a filler prevents the decrease in activation energy over the course of the experiments. Thus, the PLA/starch composite is more resistant to the two aging conditions than the pure PLA. When considering the mechanical properties, the pure PLA showed a large deviation of results compared to the initial value in a range of +63.88% to −33.96% with regard to the respective aging conditions, whereas the PLA/starch composite properties nearly always remained at the initial values. Through the investigation of the mechanical and thermal properties, it was shown that the steady activation energies are consistent with the mechanical properties, as these have shown only a small deviation of the mechanical properties during the duration of experiments for the PLA/starch composite.

在这项研究中,半结晶聚乳酸和含有 50 wt.% 原生马铃薯淀粉的复合材料被混合并注塑成型。通过拉伸、三点弯曲和夏比冲击试验对材料进行了机械表征。这些测试分别在新模塑状态下以及在加速温度或湿度条件下存放 332 小时和 792 小时后进行。采用 Flynn-Wall-Ozawa 方法计算了各自的活化能。研究的重点是调查活化能与相关机械和热性能之间的相关性。结果表明,添加原生马铃薯淀粉作为填料可防止活化能在实验过程中降低。因此,聚乳酸/淀粉复合材料比纯聚乳酸更能抵抗两种老化条件。在考虑机械性能时,纯聚乳酸在不同老化条件下的结果与初始值相比偏差较大,范围在 +63.88% 到 -33.96% 之间,而聚乳酸/淀粉复合材料的性能几乎始终保持在初始值。通过对机械性能和热性能的研究表明,稳定的活化能与机械性能是一致的,因为在聚乳酸/淀粉复合材料的实验过程中,机械性能只出现了很小的偏差。
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引用次数: 0
The energy landscape of the ribosome 核糖体的能量景观
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2023-12-05 DOI: 10.1002/bip.23570
Sandra Byju, Asem Hassan, Paul C. Whitford

The ribosome is a prototypical assembly that can be used to establish general principles and techniques for the study of biological molecular machines. Motivated by the fact that the dynamics of every biomolecule is governed by an underlying energy landscape, there has been great interest to understand and quantify ribosome energetics. In the present review, we will focus on theoretical and computational strategies for probing the interactions that shape the energy landscape of the ribosome, with an emphasis on more recent studies of the elongation cycle. These efforts include the application of quantum mechanical methods for describing chemical kinetics, as well as classical descriptions to characterize slower (microsecond to millisecond) large-scale (10–100 Å) rearrangements, where motion is described in terms of diffusion across an energy landscape. Together, these studies provide broad insights into the factors that control a diverse range of dynamical processes in this assembly.

核糖体是一种典型的组装体,可用于建立研究生物分子机器的一般原则和技术。每种生物分子的动力学都受潜在能量景观的支配,受这一事实的激励,人们对理解和量化核糖体能量产生了极大的兴趣。在本综述中,我们将重点介绍塑造核糖体能谱的相互作用的理论和计算策略,并着重介绍最近对延伸周期的研究。这些工作包括应用量子力学方法描述化学动力学,以及应用经典描述方法描述较慢(微秒到毫秒)的大规模(10-100 Å)重排,其中运动是通过能量景观的扩散来描述的。总之,这些研究为我们提供了广泛的见解,让我们了解控制这种组装中各种动态过程的因素。
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引用次数: 0
Structural, material and antibacterial properties of quercetin incorporated soy protein isolate films and its binding behavior through molecular docking 槲皮素结合大豆分离蛋白膜的结构、材料和抗菌性能及其分子对接的结合行为。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2023-11-16 DOI: 10.1002/bip.23569
Priya Rani, Piyush Kumar Yadav, Ajay Kumar Singh, Suman Nayak, K. Dinesh Kumar, Rakesh Kumar

This study aimed to investigate the three different methods for the fabrication of quercetin (1%–3% w/w of protein) incorporated soy protein isolate (SPI) films and their effect on material properties. The quercetin incorporated SPI films prepared by these methods were characterized by Fourier transform infrared (FTIR) spectroscopy, UV–Vis spectrophotometer, tensile properties, and water uptake and leaching properties. The cross-linking pattern was revealed by the FTIR spectrum that showed formation of an ester group because of interaction between the quercetin hydroxyl group and the carboxyl side chain of SPI amino acids. The tensile strength of SPI films were enhanced with the addition of quercetin as it increased to a maximum of 6.17 MPa while neat SPI film had tensile strength 4.13 MPa. The prepared films exhibit significant antibacterial activity against Listeria monocytogenes and Escherichia coli. The In-silico docking analysis demonstrates that covalent and non-covalent forces play crucial roles in binding interaction. It shows the formation of four hydrogen bonds, two salt bridges along with one pi-alkyl interaction. The simulation studies reflect the crucial amino acid residues involved in SPI-quercetin binding. The effect of quercetin binding with SPI on its stability and compactness is revealed by Root mean square deviation (RMSD) and radius of gyration studies.

研究了槲皮素(1% ~ 3% w/w)大豆分离蛋白(SPI)膜的三种不同制备方法及其对材料性能的影响。采用傅里叶变换红外光谱(FTIR)、紫外可见分光光度计、拉伸性能、吸水浸出性能等对制备的槲皮素掺入SPI膜进行了表征。FTIR光谱显示槲皮素羟基与SPI氨基酸羧基侧链相互作用形成酯基。槲皮素的加入提高了SPI膜的抗拉强度,最高可达6.17 MPa,而纯SPI膜的抗拉强度为4.13 MPa。所制备的薄膜对单核增生李斯特菌和大肠杆菌具有明显的抑菌活性。硅对接分析表明,共价力和非共价力在结合相互作用中起关键作用。它显示了四个氢键的形成,两个盐桥以及一个pi-烷基相互作用。模拟研究反映了参与spi -槲皮素结合的关键氨基酸残基。通过均方根偏差(RMSD)和旋转半径研究揭示了槲皮素与SPI结合对其稳定性和致密性的影响。
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引用次数: 0
Innovations in applications and prospects of non-isocyanate polyurethane bioplastics 非异氰酸酯聚氨酯生物塑料的应用创新与前景。
IF 2.9 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2023-10-17 DOI: 10.1002/bip.23568
Mangal Mangal, Supriya H., Suryasarathi Bose, Tamal Banerjee

Currently, conventional plastics are necessary for a variety of aspects of modern daily life, including applications in the fields of healthcare, technology, and construction. However, they could also contain potentially hazardous compounds like isocyanates, whose degradation has a negative impact on both the environment and human health. Therefore, researchers are exploring alternatives to plastic which is sustainable and environmentally friendly without compromising its mechanical and physical features. This review study highlights the production of highly eco-friendly bioplastic as an efficient alternative to non-biodegradable conventional plastic. Bioplastics are produced from various renewable biomass sources such as plant debris, fatty acids, and oils. Poly-addition of di-isocyanates and polyols is a technique employed over decades to produce polyurethanes (PUs) bioplastics from renewable biomass feedstock. The toxicity of isocyanates is a major concern with the above-mentioned approach. Novel green synthetic approaches for polyurethanes without using isocyanates have been attracting greater interest in recent years to overcome the toxicity of isocyanate-containing raw materials. The polyaddition of cyclic carbonates (CCs) and polyfunctional amines appears to be the most promising method to obtain non-isocyanate polyurethanes (NIPUs). This method results in the creation of polymeric materials with distinctive and adaptable features with the elimination of harmful compounds. Consequently, non-isocyanate polyurethanes represent a new class of green polymeric materials. In this review study, we have discussed the possibility of creating novel NIPUs from renewable feedstocks in the context of the growing demand for efficient and ecologically friendly plastic products.

目前,传统塑料在现代日常生活的各个方面都是必要的,包括在医疗保健、技术和建筑领域的应用。然而,它们也可能含有潜在的危险化合物,如异氰酸酯,其降解对环境和人类健康都有负面影响。因此,研究人员正在探索在不影响其机械和物理特性的情况下可持续、环保的塑料替代品。这项综述研究强调了生产高度环保的生物塑料,作为不可生物降解的传统塑料的有效替代品。生物塑料由各种可再生生物质来源生产,如植物碎屑、脂肪酸和油。二异氰酸酯和多元醇的聚加成是一种几十年来使用可再生生物质原料生产聚氨酯(PU)生物塑料的技术。异氰酸酯的毒性是上述方法的主要问题。近年来,为了克服含异氰酸酯原料的毒性,不使用异氰酸酯的新型绿色合成聚氨酯方法引起了人们的极大兴趣。环状碳酸酯(CC)和多官能胺的加聚似乎是获得非异氰酸酯聚氨酯(NIPU)的最有前途的方法。这种方法产生了具有独特和适应性的聚合物材料,并消除了有害化合物。因此,非异氰酸酯聚氨酯代表了一类新的绿色聚合物材料。在这项综述研究中,我们讨论了在对高效和生态友好的塑料产品需求不断增长的背景下,用可再生原料生产新型NIPU的可能性。
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引用次数: 0
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