Glutaral

Glutaral
  • 文章类型: Journal Article
    目的:测试虹鳟鱼皮肤作为手术网片在大鼠腹部疝中的应用。
    方法:实验涉及20只Wistar大鼠,接受鳟鱼皮植入物,在0.5%戊二醛中进行消毒处理,并在100%甘油中保存。这些动物被分成四组,在术后7、15、30和90天分开。进行了临床和红外热成像评估,安乐死之后,进行粘连形成的评估和用于组织学评估的样品收集。
    结果:观察到植入物完好无损,确保腹壁的完整性,支持内脏,和大鼠的正常活动长达90天。观察到临床改变率低,在第7天有强烈的炎症反应,在第15天有慢性炎症和血管生成的发作,在第30天有胶原浸润和纤维化的低炎症反应。在第90天,植入物显示胶原和纤维化浸润,具有最小的炎性浸润。
    结论:鳟鱼皮肤的外科网片表现良好,使其成为腹壁肌肉腱膜矫正手术的潜在替代方法。
    OBJECTIVE: To test the use of rainbow trout skin as a surgical mesh in abdominal hernioplasties in rats.
    METHODS: The experiment involved 20 Wistar rats receiving implants of trout skin processed for disinfection in 0.5% glutaraldehyde and preserved in 100% glycerin. The animals were divided into four groups, divided at 7, 15, 30, and 90 days postoperatively. Clinical and infrared thermography evaluations were performed, and after euthanasia, assessments of adhesion formations and sample collection for histological evaluation were conducted.
    RESULTS: The implant was observed to be intact, ensuring the integrity of the abdominal wall, support for the viscera, and normal mobility for the rats for up to 90 days. Low rates of clinical alterations were observed, with an intense inflammatory reaction up to day 7, chronic inflammation and the onset of angiogenesis at day 15, and a low inflammatory reaction with collagenous infiltrate and fibrosis at day 30. At day 90, the implants showed a collagenous and fibrotic infiltrate with a minimal inflammatory infiltrate.
    CONCLUSIONS: The surgical mesh of trout skin performed well, making it a potential alternative for surgical procedures in muscle aponeurotic corrections in the abdominal wall.
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  • 文章类型: Case Reports
    背景:目前的研究提出了一种新颖而精确的手术技术,用于在主动脉瓣疾病和心内膜炎患者中使用戊二醛处理的自体心包完全重建主动脉瓣。该技术旨在为主动脉瓣修复提供一种更有效和可重复的方法,目的是改善主动脉瓣疾病患者的预后和生活质量。
    方法:一名35岁的伊朗男性主动脉瓣疾病和心内膜炎患者接受了主动脉瓣重建手术。术前超声心动图显示主动脉瓣变性伴严重反流,左心室射血分数降低,和特定的主动脉根部尺寸。手术技术涉及精确测量和计算,以使用自体心包设计新的主动脉瓣尖的大小和形状,以优化接合和功能为目标。外科医生基于主动脉瓣环直径计算连合间距离以确定尖点大小和形状。他调整了心包尖端,使其高度等于接合边缘长度的80%。使用详细的缝合技术来确保新尖的正确对齐和接合。术中使用抽吸和经食管超声心动图评估瓣膜功能显示良好的接合和最小的残留反流。在3年的随访中,患者的主动脉瓣功能良好,只有轻微的渗漏,临床状况令人满意。
    结论:戊二醛处理的自体心包是一种有效的小叶替代品,其失败的原因是晚期环形扩张和其他技术故障。目前的证据表明,用戊二醛处理的自体心包重建主动脉瓣具有许多优点,具有改善患者预后和生活质量的潜力。需要进一步的临床研究来评估这种方法的长期耐久性和有效性。
    BACKGROUND: The current study presents a novel and precise surgical technique for complete reconstruction of the aortic valve using glutaraldehyde-treated autologous pericardium in a patient with aortic valve disease and endocarditis. The technique aims to provide a more effective and reproducible method for aortic valve repair, with the goal of improving outcomes and quality of life for patients with aortic valve disease.
    METHODS: A 35-year-old Iranian male with aortic valve disease and endocarditis underwent aortic valve reconstruction surgery. Preoperative echocardiography showed a degenerative aortic valve with severe regurgitation, reduced left ventricular ejection fraction, and specific aortic root dimensions. The surgical technique involved precise measurements and calculations to design the size and shape of the new aortic valve cusps using autologous pericardium, with the goal of optimizing coaptation and function. The surgeon calculated the intercommissural distance based on the aortic annulus diameter to determine cusp size and shape. He tailored the pericardial cusps to have a height equal to 80% of the coaptation margin length. Detailed suturing techniques were used to ensure proper alignment and coaptation of the new cusps. Intraoperative evaluation of the valve function using suction and transesophageal echocardiography showed good coaptation and minimal residual regurgitation. At the 3-year follow-up, the patient had a well-functioning aortic valve with only trivial leak and was in satisfactory clinical condition.
    CONCLUSIONS: Glutaraldehyde-treated autologous pericardium is a validated leaflet alternative, and the causes of its failure are late annular dilatation and other technique breakdowns. Current evidence reveals that aortic valve reconstruction with glutaraldehyde-treated autologous pericardium is associated with many advantages with the potential to improve patient outcomes and quality of life. Further clinical studies are warranted to evaluate the long-term durability and efficacy of this approach.
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  • 文章类型: Journal Article
    这项工作旨在提高可重复使用的碘化钾水凝胶剂的后稳定性。一种可重复使用且低成本的放射变色剂量计,其中包含聚乙烯醇的凝胶基质,碘化钾染料,开发了氟乳糖作为还原剂和戊二醛作为交联剂用于放射治疗剂量校准。使用医用线性加速将凝胶样品暴露于不同的吸收剂量。UV-Vis分光光度法用于研究辐照凝胶的光学性质相对于353nm的峰值波长的变化。通过添加一定浓度的二甲基亚砜,凝胶的稳定性(使用该剂量计的最大限制之一)得到了显着改善。具有均匀RGB发光二极管(LED)阵列源的电荷耦合器件(CCD)相机的二维光学成像系统使用二维凝胶模板用于扩散系数目的。与文献中报道的其他剂量计相比,报道的扩散系数的值是显着的并且大大降低。此外,将改进的凝胶加热到一定的温度导致其光学性能的重置,这使得可以重复使用多次。
    This work aims to improve the post stabilty of reusable potassium iodide hydrogel dosimter. A reusable and low-cost radiochromic dosimeter containing a gel matrix of polyvinyl alcohol, potassium iodide dye, froctose as reducing agent and glutaraldehyde as cross-linking agent was developed for dose calibration in radiotherapy. The gel samples were exposed to different absorbed doses using a medical linear acceleration. UV-vis Spectrophotometry was utilized to investigate the changes in optical-properties of irradiated gels with regard to peak wavelength of 353 nm. The stability of the gel (one of the most limitation of using this dosimeter) was improved significantly by the addition of certain concentrations of dimethyl sulfoxide. The two-dimensional optical imaging system of charge-coupled-device (CCD) camera with a uniform RGB light-emitting-diode (LED) array source was used for diffusion coefficient purpose using two dimensional gel template. The value of diffusion coefficient reported is significant and highly reduced compared with other dosimeters reported in the literatures. Moreover, heating the improved gels to certain temperatures results in resetting their optical properties, which makes it possible to reuse for multiple times.
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  • 文章类型: Journal Article
    通过使用氟化铵作为扩孔剂以促进TLL固定,将毛藻木霉脂肪酶(TLL)吸附到未煅烧(SBAUC-TLL)和煅烧(SBAC-TLL)SBA-15上,制备了非均相生物催化剂。在1mg/g的酶负荷下,实现了高固定化产率(>90%)和回收活性(SBAUC-TLL>80%和SBAC-TLL>70%)。当将酶负荷增加到5mg/g时,SBAUC-TLL的固定化产率为80%,恢复的活性为50%,而SBAC-TLL具有100%的产率和36%的恢复活性。进行与戊二醛(GA)的交联以改善稳定性(SBAUC-TLL-GA和SBAC-TLL-GA)。虽然SBAC-TLL-GA在GA修饰后失去了25%的初始活性,它表现出最高的热量(t1/2=5.7小时,在65°C),与SBAC-TLL(t1/2=12分钟)和可溶性酶(t1/2=36分钟)相比,和操作稳定性(5个循环后保持100%活性)。两种生物催化剂均呈现高储存稳定性,因为它们保持100%的初始活性持续30天。这些结果突出了SBA-15作为酶支持的潜力和方案在增强稳定性方面的功效,对食品工业应用的影响,化学,和制药部门。
    Heterogeneous biocatalysts were prepared by adsorbing T. lanuginosus lipase (TLL) onto uncalcined (SBAUC-TLL) and calcined (SBAC-TLL) SBA-15, using ammonium fluoride as a pore expander to facilitate TLL immobilization. At an enzyme load of 1 mg/g, high immobilization yields (>90 %) and recovered activities (>80 % for SBAUC-TLL and 70 % for SBAC-TLL) were achieved. When increasing the enzyme load to 5 mg/g, the immobilization yield of SBAUC-TLL was 80 %, and the recovered activity was 50 %, while SBAC-TLL had a yield of 100 % and a recovered activity of 36 %. Crosslinking with glutaraldehyde (GA) was conducted to improve stability (SBAUC-TLL-GA and SBAC-TLL-GA). Although SBAC-TLL-GA lost 25 % of initial activity after GA modifications, it exhibited the highest thermal (t1/2 = 5.7 h at 65 °C), when compared to SBAC-TLL (t1/2 = 12 min) and the soluble enzyme (t1/2 = 36 min), and operational stability (retained 100 % activity after 5 cycles). Both biocatalysts presented high storage stability since they retained 100 % of initial activity for 30 days. These results highlight SBA-15\'s potential as an enzyme support and the protocol\'s efficacy in enhancing stability, with implications for industrial applications in the food, chemical, and pharmaceutical sectors.
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  • 文章类型: Journal Article
    我们介绍了来自Megathyrsusmaximus(几内亚草)(GGP)的过氧化物酶的交联酶聚集体(CLEAS)的合成。在搅拌下使用50%v/v乙醇和0.88%w/v戊二醛持续1小时制备生物催化剂。固定化产率为93.74%,比活性为36.75Umg-1。在最佳pH值(两种制剂的pH均为6)下,生物催化剂的游离酶活性超过了61%,在pH9时,活性几乎增加了10倍。GGP-CLEAS表现出比游离酶更高的热稳定性(2-4倍),并且对过氧化氢更稳定(2-3倍)。GGP-CLEAS在反应60分钟后,在存在0.55mMH2O2的情况下,在pH5下去除超过80%的0.05mM靛蓝。比使用游离酶高得多的价值。操作稳定性显示酶活性下降(4个循环超过60%),很可能与自杀抑制有关。
    We present the synthesis of a cross-linking enzyme aggregate (CLEAS) of a peroxidase from Megathyrsus maximus (Guinea Grass) (GGP). The biocatalyst was produced using 50%v/v ethanol and 0.88%w/v glutaraldehyde for 1 h under stirring. The immobilization yield was 93.74% and the specific activity was 36.75 U mg-1. The biocatalyst surpassed by 61% the free enzyme activity at the optimal pH value (pH 6 for both preparations), becoming this increase in activity almost 10-fold at pH 9. GGP-CLEAS exhibited a higher thermal stability (2-4 folds) and was more stable towards hydrogen peroxide than the free enzyme (2-3 folds). GGP-CLEAS removes over 80% of 0.05 mM indigo carmine at pH 5, in the presence of 0.55 mM H2O2 after 60 min of reaction, a much higher value than when using the free enzyme. The operational stability showed a decrease of enzyme activity (over 60% in 4 cycles), very likely related to suicide inhibition.
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  • 文章类型: Journal Article
    生物电化学系统(BES),特别是微生物燃料电池(MFC),已经成为环境生物技术中有前途的技术。本研究的重点是优化阳极细菌培养固定化工艺以提高BES性能。该研究结合并修改了两种关键的固定方法:与戊二醛的共价键合和包含在壳聚糖凝胶中,以满足MFC中生物阳极的标准和要求。在平行实验中比较了固定化和悬浮培养物的MFC的性能。考虑到较低的生物质浓度,两种类型的底物利用动态相似,固定化生物阳极的优势很小。固定化MFC表现出更高的发电和代谢活性,也是。可能,这是由于改进的阳极呼吸和更高的库仑效率的反应器。有机酸含量的分析支持了这一结论,表明在固定化阳极培养的MFC反应器中发酵产物的生产受到显着抑制。
    Bio-electrochemical Systems (BES), particularly Microbial Fuel Cells (MFC), have emerged as promising technologies in environmental biotechnology. This study focused on optimizing the anode bacterial culture immobilization process to enhance BES performance. The investigation combines and modifies two key immobilization methods: covalent bonding with glutaraldehyde and inclusion in a chitosan gel in order to meet the criteria and requirements of the bio-anodes in MFC. The performance of MFCs with immobilized and suspended cultures was compared in parallel experiments. Both types showed similar substrate utilization dynamics with slight advantage of the immobilized bio-anode considering the lower concentration of biomass. The immobilized MFC exhibited higher power generation and metabolic activity, as well. Probably, this is due to improved anodic respiration and higher coulombic efficiency of the reactor. Analysis of organic acids content supported this conclusion showing significant inhibition of the fermentation products production in the MFC reactor with immobilized anode culture.
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  • 文章类型: Journal Article
    目的:比较蜂胶和gluma脱敏剂对牙本质过敏的治疗效果。
    方法:单盲,随机对照试验在牙科手术部进行,IshratulEbadKhan口腔健康科学研究所博士,陶氏健康科学大学,卡拉奇,从2020年10月至2021年9月,包括牙本质过敏症患者,其疼痛评分在视觉模拟量表上至少为2分。将牙齿随机分为蜂胶A组和GlumaB组,使用视觉模拟评分和Schiff's敏感性评分评估基线疼痛评分,并与干预后立即评分进行比较。然后经过一周零一个月的干预。数据采用SPSS23进行分析。
    结果:在22例患者中,女性12人(54.5%),男性10人(45.4%)。在80颗牙齿中,两组各40例(50%).在施用脱敏剂后立即观察到牙本质过敏的显著降低(p<0.05)。然而,一个月后,Gluma比蜂胶更有效(p<0.05)。
    结论:发现Gluma和蜂胶都是有效的脱敏剂,但是蜂胶的有效性在一个月内下降。
    临床试验:NCT04819867。
    OBJECTIVE: To compare the effect of propolis and gluma desensitisers on the management of dentin hypersensitivity.
    METHODS: The single-blind, randomised controlled trial was conducted at the Department of Operative Dentistry, Dr Ishrat ul Ebad Khan Institute of Oral Health Sciences, Dow University of Health Sciences, Karachi, from October 2020 to September 2021, and comprised patients with dentin hypersensitivity who had pain scores of at least 2 on the visual analogue scale. The teeth were randomised into propolis group A and Gluma group B. Baseline pain scores were assessed using visual analogue scale and Schiff\'s sensitivity scores and compared with scores immediately after the intervention, and then after one week and one month of the intervention. Data was analysed using SPSS 23.
    RESULTS: Of the 22 patients, 12(54.5%) were females and 10(45.4%) were males. Of the 80 teeth, there were 40(50%) in each of the 2 groups. Significant reduction was observed in dentin hypersensitivity immediately after the application of the desensitising agents (p<0.05). However, after one month, Gluma was more effective than propolis (p<0.05).
    CONCLUSIONS: Both Gluma and propolis were found to be effective desensitising agents, but the effectiveness of propolis decreased over one month.
    UNASSIGNED: Clinical Trials.gov: NCT04819867.
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  • 文章类型: Journal Article
    背景:乙烯基聚醚有机硅(VPES)是由乙烯基聚硅氧烷(VPS)和聚醚(PE)的组合制成的新型印模生物材料。因此,在各种消毒剂测试条件下评估其特性和行为非常重要。本研究旨在评估新型VPES印模材料在标准消毒剂中浸泡不同时间间隔后的尺寸稳定性。
    方法:使用的弹性印模材料-中等身体常规组(单相)[Exa\'lenceGCAmerica]。使用不锈钢模具和环(ADA规格19)制造总共84个样品。将这些样品分配到对照组(n=12)和测试组(n=72)中。试验组分为3组,根据使用的消毒剂类型-A组-2%戊二醛,B-0组。基于每个样品浸入消毒剂的时间间隔,将每个测试组的5%次氯酸钠和C-2%氯己定进一步分为2个亚组(n=12/亚组)-亚组-1-10分钟和亚组-30分钟。印模材料设置后,将其从环中取出,然后在水中洗涤15秒。立即在立体显微镜上进行对照组测量,并将其他样品浸入三种消毒溶液中10分钟和30分钟,以通过使用立体显微镜在X40放大倍数下测量由不锈钢模具在样品上产生的线之间的距离来检查尺寸稳定性。
    结果:在对照组中测得的距离为4397.2078µm和4396.1571µm;对于测试组,A-2%戊二醛为4396.4075µm和4394.5992µm;B-0组。5%次氯酸钠为4394.5453µm和4389.4711µm组-C-2%氯己定分别为4395.2953µm和4387.1703µm,持续10分钟和30分钟。对于所有组10分钟和30分钟,尺寸变化百分比在0.02-0.25的范围内。
    结论:2%戊二醛在尺寸稳定性方面是最适合用于VPES弹性印模材料的消毒剂,并且与2%氯己定和0.5%次氯酸钠相比显示最小的尺寸变化。
    BACKGROUND: Vinyl polyether silicone (VPES) is a novel impression biomaterial made of a combination of vinyl polysiloxane (VPS) and polyether (PE). Thus, it is significant to assess its properties and behaviour under varied disinfectant test conditions. This study aimed to assess the dimensional stability of novel VPES impression material after immersion in standard disinfectants for different time intervals.
    METHODS: Elastomeric impression material used -medium body regular set (Monophase) [Exa\'lence GC America]. A total of 84 Specimens were fabricated using stainless steel die and ring (ADA specification 19). These samples were distributed into a control group (n=12) and a test group (n=72). The test group was divided into 3 groups, based on the type of disinfectant used - Group-A- 2% Glutaraldehyde, Group-B- 0. 5% Sodium hypochlorite and Group-C- 2% Chlorhexidine each test group was further divided into 2 subgroups (n=12/subgroup) based on time intervals for which each sample was immersed in the disinfectants - subgroup-1- 10 mins and Subgroup 2- 30 mins. After the impression material was set, it was removed from the ring and then it was washed in water for 15 seconds. Control group measurements were made immediately on a stereomicroscope and other samples were immersed in the three disinfection solutions for 10 mins and 30 mins to check the dimensional stability by measuring the distance between the lines generated by the stainless steel die on the samples using a stereomicroscope at x40 magnification.
    RESULTS: The distance measured in the control group was 4397.2078 µm and 4396.1571 µm; for the test group Group-A- 2% Glutaraldehyde was 4396.4075 µm and 4394.5992 µm; Group-B- 0. 5% Sodium hypochlorite was 4394.5453 µm and 4389.4711 µm Group-C- 2% Chlorhexidine was 4395.2953 µm and 4387.1703 µm respectively for 10 mins and 30 mins. Percentage dimensional change was in the range of 0.02 - 0.25 for all the groups for 10 mins and 30 mins.
    CONCLUSIONS: 2 % Glutaraldehyde is the most suitable disinfectant for VPES elastomeric impression material in terms of dimensional stability and shows minimum dimensional changes as compared to that of 2% Chlorhexidine and 0.5% Sodium hypochlorite.
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  • 文章类型: Journal Article
    米曲霉β-D-半乳糖苷酶(β-Gal)能有效地将芝麻酚三葡萄糖苷水解为芝麻酚,具有较高的生物活性。然而,β-Gal难以从反应混合物中分离并且受到稳定性的限制。为了解决这些问题,将β-Gal固定在戊二醛预活化的氨基功能化磁性纳米颗粒介孔二氧化硅(Fe3O4@mSiO2-β-Gal)上,首次用于制备芝麻酚。在最优条件下,β-Gal的固定化产率和回收活性分别为57.9±0.3%和46.5±0.9%,酶载量为843±21酶/gsupport。通过各种表征方法证实了Fe3O4@mSiO2-β-Gal的构建,结果表明,它适用于非均相酶催化反应。Fe3O4@mSiO2-β-Gal在磁作用下易于分离,并在极端pH和温度条件下显示出改善的活性。在4°C下储存45天后,Fe3O4@mSiO2-β-Gal的活性保持在92.3±2.8%,是游离酶的1.29倍,10个周期后其活性保持在85%以上。Fe3O4@mSiO2-β-Gal表现出更高的亲和力和催化效率。在55.0°C时,半衰期比游离酶长1.41。以Fe3O4@mSiO2-β-Gal为催化剂制备芝麻酚,芝麻酚的转化率为96.7%。优异的稳定性和催化效率为生物催化工业应用提供了广泛的益处和潜力。
    Aspergillus oryzae β-D-galactosidase (β-Gal) efficiently hydrolyzes sesaminol triglucoside into sesaminol, which has higher biological activity. However, β-Gal is difficult to be separate from the reaction mixture and limited by stability. To resolve these problems, β-Gal was immobilized on amino-functionalized magnetic nanoparticles mesoporous silica pre-activated with glutaraldehyde (Fe3O4@mSiO2-β-Gal), which was used for the first time to prepare sesaminol. Under the optimal conditions, the immobilization yield and recovered activity of β-Gal were 57.9 ± 0.3 % and 46.5 ± 0.9 %, and the enzymatic loading was 843 ± 21 Uenzyme/gsupport. The construction of Fe3O4@mSiO2-β-Gal was confirmed by various characterization methods, and the results indicated it was suitable for heterogeneous enzyme-catalyzed reactions. Fe3O4@mSiO2-β-Gal was readily separable under magnetic action and displayed improved activity in extreme pH and temperature conditions. After 45 days of storage at 4 °C, the activity of Fe3O4@mSiO2-β-Gal remained at 92.3 ± 2.8 %, which was 1.29 times than that of free enzyme, and its activity remained above 85 % after 10 cycles. Fe3O4@mSiO2-β-Gal displayed higher affinity and catalytic efficiency. The half-life was 1.41 longer than free enzymes at 55.0 °C. Fe3O4@mSiO2-β-Gal was employed as a catalyst to prepare sesaminol, achieving a 96.7 % conversion yield of sesaminol. The excellent stability and catalytic efficiency provide broad benefits and potential for biocatalytic industry applications.
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  • 文章类型: Journal Article
    在这篇文章中,在三个不同的时间点(60分钟,90分钟,和120分钟),使用固定化胃蛋白酶在活性炭和改性碳上(AC,ACF,ACG50,ACG100)。固定化试验表明,与游离酶相比,生物催化剂的活性降低。在修改的那些中,ACG50在重复使用周期中表现出更高的活性和更高的效率,60分钟和90分钟后具有优异的值。在所有研究条件下观察到肽合成。分析(DPPH,β-胡萝卜素/亚油酸,FRAP)证实了固定化酶产生的肽的抗氧化潜力。然而,ACG50和ACG100中的固定化酶,结合更长的水解时间,允许形成抗氧化能力大于或等于游离酶产生的肽,尽管酶活性降低。
    In this article, the synthesis of antioxidant peptides in the enzymatic hydrolysis of caprine casein was analyzed at three different time points (60 min, 90 min, and 120 min) using immobilized pepsin on activated and modified carbon (AC, ACF, ACG 50, ACG 100). The immobilization assays revealed a reduction in the biocatalysts\' activity compared to the free enzyme. Among the modified ones, ACG 50 exhibited greater activity and better efficiency for reuse cycles, with superior values after 60 min and 90 min. Peptide synthesis was observed under all studied conditions. Analyses (DPPH, β-carotene/linoleic acid, FRAP) confirmed the antioxidant potential of the peptides generated by the immobilized enzyme. However, the immobilized enzyme in ACG 50 and ACG 100, combined with longer hydrolysis times, allowed the formation of peptides with an antioxidant capacity greater than or equivalent to those generated by the free enzyme, despite reduced enzymatic activity.
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