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Application of mitochondrial genomes to species identification and evolution 线粒体基因组在物种鉴定和进化中的应用
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-07-01 Epub Date: 2025-06-02 DOI: 10.1016/j.ejbt.2025.04.001
Bingpeng Xing , Liangyu Lin , Qiong Wu
Mitochondrial genomes (mtDNA) have become invaluable in species classification and evolutionary studies due to their unique characteristics, including maternal inheritance, and high mutation rates. This review examines the application of mtDNA in tracing evolutionary history, elucidating phylogenetic relationships, and understanding mechanisms of species divergence. The evolution of mitochondrial DNA research from its initial focus on energy metabolism to its current role in biodiversity assessments highlights its significance in modern biology. Mitochondrial DNA barcoding, particularly utilizing the cytochrome c oxidase I (COI) gene, has revolutionized species identification, enabling rapid and accurate classification across diverse taxa. The article further explores the implications of mtDNA in understanding adaptive evolution, as genetic variations within mitochondrial genomes can reveal insights into how species respond to environmental pressures. However, challenges such as gene mixing, hybridization, and incomplete lineage sorting can complicate interpretations of mtDNA data. Thus, integrating mitochondrial with nuclear genome data is advocated to provide a comprehensive view of species relationships and evolutionary patterns. Future research directions emphasize the need for multi-genome studies, investigations into ecological adaptations, and exploration of understudied taxa and ecosystems, which are crucial for enhancing our understanding of biodiversity and informing conservation strategies.
How to cite: Xing B, Lin L, Wu Q. Application of mitochondrial genomes to species identification and evolution. Electron J Biotechnol 2025;76. https://doi.org/10.1016/j.ejbt.2025.04.001.
线粒体基因组(mtDNA)由于其独特的特征,包括母系遗传和高突变率,在物种分类和进化研究中变得非常宝贵。本文综述了mtDNA在追溯进化历史、阐明系统发育关系和理解物种分化机制方面的应用。线粒体DNA研究从最初关注能量代谢到目前在生物多样性评估中的作用的演变凸显了其在现代生物学中的重要意义。线粒体DNA条形码,特别是利用细胞色素c氧化酶I (COI)基因,已经彻底改变了物种鉴定,使不同分类群之间的快速和准确分类成为可能。本文进一步探讨了mtDNA在理解适应性进化中的意义,因为线粒体基因组中的遗传变异可以揭示物种如何应对环境压力。然而,诸如基因混合、杂交和不完整谱系分类等挑战会使mtDNA数据的解释复杂化。因此,建议将线粒体与核基因组数据整合起来,以提供对物种关系和进化模式的全面看法。未来的研究方向强调多基因组研究、生态适应性研究以及对未被充分研究的分类群和生态系统的探索,这对提高我们对生物多样性的认识和制定保护策略至关重要。邢斌,林林,吴强。线粒体基因组在物种鉴定和进化中的应用。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.04.001。
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引用次数: 0
The evolution of isothermal amplification technology: A bibliometric study (2013–2022) 等温扩增技术的演变:文献计量学研究(2013-2022)
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-07-01 Epub Date: 2025-05-09 DOI: 10.1016/j.ejbt.2025.03.003
Hanting Zhu , Zhitong Miao , Junfei Yuan , Wanying Xie , Qiaoqiao Zhang , Kun Yang

Background

Isothermal amplification is a nucleic acid amplification technology (NAAT) that has contributed significantly to molecular diagnostics. The combination of NAAT with a suitable detection platform has improved sensitivity and specificity and enabled rapid disease diagnosis. A total of 5388 articles relating to isothermal amplification technology published from 2013 to 2022 were identified in the Web of Science Core Collection (WoSCC) database and subsequently analyzed with CiteSpace 5.7.R1 software.

Results

The number of published articles on isothermal amplification technology steadily increased between 2013 and 2022. The disciplines included Chemistry, Science Technology Other Topics, Biotechnology Applied Microbiology, Microbiology, and Biochemistry Molecular Biology. The countries with the highest number of published articles were China, the United States, and Japan while the institutions with the highest number of published articles were the Chinese Academy of Sciences, the Chinese Academy of Agricultural Sciences, and Mahidol University. The high-frequency keywords included rapid detection, sensitivity, pathogen, Escherichia coli, probe, primer, and expression. Over recent years, most research studies concerning isothermal amplification focused on its advantages, improvements, and applications. RCA, LAMP, RPA, and Cas technologies appeared sequentially from 2013 onward. The keyword “LAMP” exhibited the highest frequency (1222 times).

Conclusions

Our study described the research trends and the status of isothermal amplification technology over the past decade, providing guidance for future research in this field.
How to cite: Zhu H, Miao Z, Yuan J, et al. The evolution of isothermal amplification technology: A bibliometric study (2013–2022). Electron J Biotechnol 2025;76. https://doi.org/10.1016/j.ejbt.2025.03.003.
二温扩增是一种核酸扩增技术,在分子诊断中有着重要的作用。NAAT与合适的检测平台结合,提高了敏感性和特异性,实现了疾病的快速诊断。从Web of Science Core Collection (WoSCC)数据库中检索2013 - 2022年间发表的5388篇与等温扩增技术相关的文献,并利用CiteSpace 5.7进行分析。R1软件。结果2013 - 2022年,等温扩增技术相关论文数量稳步增长。学科包括化学、科学技术及其他课题、生物科技应用微生物学、微生物学及生物化学分子生物学。发表论文数量最多的国家是中国、美国和日本,而发表论文数量最多的机构是中国科学院、中国农业科学院和玛希隆大学。高频关键词包括快速检测、敏感性、病原菌、大肠杆菌、探针、引物、表达。近年来,关于等温扩增的研究主要集中在其优点、改进和应用上。从2013年开始,RCA、LAMP、RPA和Cas技术相继出现。关键词“LAMP”出现频率最高(1222次)。结论本研究描述了近十年来等温扩增技术的研究趋势和现状,为今后该领域的研究提供指导。引用方式:朱华,苗志,袁军,等。等温扩增技术的演变:文献计量学研究(2013-2022)。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.03.003。
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引用次数: 0
Optimizing the process conditions for the biosorption of chromium (VI) by Bacillus subtilis in artificial wastewater 优化枯草芽孢杆菌对人工废水中六价铬的生物吸附工艺条件
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-07-01 Epub Date: 2025-05-27 DOI: 10.1016/j.ejbt.2025.03.005
Khawla E. Alsamhary

Background

The contamination by heavy metals, particularly hexavalent chromium Cr (VI), is a pressing environmental concern. Cr(VI) is highly toxic, non-biodegradable and carcinogenic. Traditional remediation methods are often costly, energy-intensive, or generate secondary waste. This study explores the optimal conditions for the bacterium Bacillus subtilis in reducing Cr(VI) from synthetic wastewater.

Results

The research employed batch experiments to simulate wastewater treatment. The removal of Cr(VI) was measured spectrophotometrically. The active functional groups were studied using Fourier Transform Infrared Spectroscopy that showed an incremental shift for alkyl halides (500.75 cm−1) and OH-groups (3347 cm−1) were observed. Scanning Electron Microscopy images demonstrated that the surface morphology of the biosorbent was more homogenous before than after adsorption. The biosorbent’s structure was confirmed by a prominent peak in X-ray Diffraction at 290.04°. The highest adsorption was observed at the adsorbent dose of 0.5 g/L, the contact time 60 min, pH 6 and temperature of 40°C. The thermodynamic parameters validated the process’s feasibility and spontaneity. Several models for biosorption kinetics and isotherm were tested. The pseudo-second-order was more suitable than the pseudo-first-order model. Langmuir isotherm model had the best fit compared to Freundlich, Dubinin–Radushkevich, and Temkin models.

Conclusions

B. subtilis appeared to be resistant to chromium and reduce Cr(VI) efficiently. This study shows the potential of B. subtilis as a viable bioremediation agent for Cr(VI) contamination in wastewater and should be studied further using real wastewater with different pollutants.
How to cite: Alsamhary KE. Optimizing the process conditions for the biosorption of chromium (VI) by Bacillus subtilis in artificial wastewater. Electron J Biotechnol 2025;76. https://doi.org/10.1016/j.ejbt.2025.03.005.
重金属污染,特别是六价铬(ⅵ)的污染,是一个紧迫的环境问题。铬(VI)是剧毒、不可生物降解的致癌物。传统的补救方法往往是昂贵的,能源密集型的,或产生二次废物。本研究探讨了枯草芽孢杆菌(Bacillus subtilis)在合成废水中还原Cr(VI)的最佳条件。结果采用批量实验模拟废水处理过程。用分光光度法测定了Cr(VI)的去除率。利用傅里叶变换红外光谱对活性官能团进行了研究,发现烷基卤化物(500.75 cm−1)和oh -基团(3347 cm−1)发生了增量位移。扫描电镜图像表明,吸附前生物吸附剂的表面形貌比吸附后更为均匀。在290.04°处的x射线衍射峰证实了生物吸附剂的结构。吸附剂用量为0.5 g/L、接触时间为60 min、pH为6、温度为40℃时,吸附效果最佳。热力学参数验证了该工艺的可行性和自发性。测试了几种生物吸附动力学和等温线模型。拟二阶模型比拟一阶模型更合适。与Freundlich、Dubinin-Radushkevich和Temkin模型相比,Langmuir等温线模型的拟合效果最好。枯草芽孢杆菌对铬具有抗性,并能有效地还原Cr(VI)。本研究表明枯草芽孢杆菌作为一种可行的废水中Cr(VI)污染的生物修复剂的潜力,需要在不同污染物的真实废水中进行进一步的研究。引用方式:alsamhari KE。优化枯草芽孢杆菌对人工废水中六价铬的生物吸附工艺条件。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.03.005。
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引用次数: 0
Response of heterotrophic nitrifying/aerobic denitrifying strain Pseudomonas stutzeri YXH-102 to hypersaline stress 异养硝化/好氧反硝化菌株stutzeri假单胞菌YXH-102对高盐胁迫的响应
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-07-01 Epub Date: 2025-06-02 DOI: 10.1016/j.ejbt.2025.05.001
Youming Wang , Zhichun Wang , Yangfan Hu , Dexun Zou , Korakot Sombatmankhong , Wen Wang , Bo Yu

Background

Hypersaline wastewater poses significant environmental challenges, necessitating efficient bioremediation strategies. This study investigates the hypersaline tolerance mechanisms of Pseudomonas stutzeri YXH-102, a heterotrophic nitrifying/aerobic denitrifying bacterium isolated from Yuncheng Salt Lake sediments, under high-salinity stress.

Results

Comparative transcriptomic analysis revealed 268 differentially expressed genes (DEGs) in response to a 10 % NaCl shock, with 86 upregulated and 182 downregulated. Key findings highlight the critical roles of oxidative stress mitigation, energy metabolism adaptation, and ion homeostasis. Salt stress triggered reactive oxygen species (ROS) accumulation, countered by upregulated cytochrome c oxidase (reducing ROS generation) and glutathione S-transferase (enhancing ROS scavenging). Concurrently, energy metabolism pathways, including fatty acid β-oxidation and acetyl-CoA production, were activated to sustain cellular energy demand. Notably, the electron transport chain (ETC) generated a robust proton motive force (PMF), which directly fueled potassium uptake via H+/K+ symporters to counteract osmotic imbalance. TonB-dependent transporters for nutrient uptake were also significantly upregulated, suggesting enhanced nutrient acquisition under salinity.

Conclusions

These findings elucidate how P. stutzeri YXH-102 combats salt stress through integrated ROS detoxification, energy optimization, and PMF-driven ion transport, providing molecular insights for its application in hypersaline wastewater bioremediation.
How to cite: Wang Y, Wang Z, Hu Y, et al. Response of heterotrophic nitrifying/aerobic denitrifying strain Pseudomonas stutzeri YXH-102 to hypersaline stress. Electron J Biotechnol 2025;76. https://doi.org/10.1016/j.ejbt.2025.05.001.
高盐废水带来了重大的环境挑战,需要有效的生物修复策略。本文研究了从运城盐湖沉积物中分离的异养硝化/好氧反硝化细菌stutzeri YXH-102在高盐胁迫下的耐盐机制。结果对比转录组学分析显示,在10% NaCl胁迫下,有268个差异表达基因(deg)表达上调,182个下调。关键发现强调了氧化应激缓解、能量代谢适应和离子稳态的关键作用。盐胁迫触发活性氧(ROS)积累,通过上调细胞色素c氧化酶(减少ROS生成)和谷胱甘肽s转移酶(增强ROS清除)来抵消。同时,能量代谢途径,包括脂肪酸β-氧化和乙酰辅酶a的产生,被激活以维持细胞的能量需求。值得注意的是,电子传递链(ETC)产生了强大的质子动力(PMF),通过H+/K+同调体直接促进钾的吸收,以抵消渗透失衡。吨位依赖性转运蛋白的营养吸收也显著上调,表明盐胁迫下营养获取增强。结论这些发现阐明了P. stutzeri YXH-102如何通过ROS解毒、能量优化和pmf驱动的离子运输来对抗盐胁迫,为其在高盐废水生物修复中的应用提供了分子视角。引用方式:王毅,王志,胡毅,等。异养硝化/好氧反硝化菌株stutzeri假单胞菌YXH-102对高盐胁迫的响应。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.05.001。
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引用次数: 0
Metformin mitigates potassium bromate-induced liver grievance in rat through attenuating NF-kB and PI3K/Akt pathway 二甲双胍通过减弱NF-kB和PI3K/Akt通路减轻溴酸钾诱导的大鼠肝脏不适
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-07-01 Epub Date: 2025-05-08 DOI: 10.1016/j.ejbt.2025.03.002
Bo Ma , Sheng Zheng , Ning Xie , Juan Yang , Xueli Zeng , Pei Liu , Shunling Zhang , Ji Li

Background

Metformin (MET) is a dietary polyphenolic compound that exhibits anti-inflammatory and antioxidant properties. This study evaluated the protective effects of MET in both in vitro and in vivo models against potassium bromate (KBrO3)-induced hepatotoxicity. Hepatic cells were exposed to KBrO3 with or without metformin (20, 40, and 60 µM), and cell viability and Reactive Oxygen Species levels were assessed. In vivo, rats were divided into five groups: control, KBrO3, and KBrO3 with metformin (25, 50, and 100 mg/kg). Liver and blood samples were analyzed for histological changes, oxidative stress markers, lipid peroxidation, liver enzymes, and PI3K/Akt signaling.

Results

KBrO3 exposure significantly decreased cell viability and increased ROS levels. Co-treatment with MET dose-dependently restored cell viability, with 60 µM MET achieving approximately 80% viability. Metformin also reduced ROS levels, with mean fluorescence intensity approaching control values at higher concentrations. In the in vivo study, KBrO3 exposure elevated lipid peroxidation markers, depleted antioxidant enzyme activities, and triggered oxidative stress and inflammation. Metformin significantly alleviated histological liver damage, suppressed proinflammatory cytokines, enhanced antioxidant enzyme activities, and modulated the PI3K/Akt signaling pathway to promote cell survival and reduce oxidative injury.

Conclusions

Metformin effectively protects hepatic cells against KBrO3-induced cytotoxicity by improving cell viability and reducing Reactive Oxygen Species levels. Metformin successfully mitigates KBrO3-induced hepatic injury by reducing oxidative stress, modulating inflammatory pathways (NF-kB), and regulating the PI3K/Akt signaling cascade, offering molecular evidence of its hepatoprotective effects.
How to cite: Ma B, Zheng S, Xie N, et al. Metformin mitigates potassium bromate induced liver grievance in rat through attenuating NF-kB and PI3K/Akt pathway. Electron J Biotechnol 2025;76. https://doi.org/10.1016/j.ejbt.2025.03.002.
二甲双胍(MET)是一种膳食多酚类化合物,具有抗炎和抗氧化特性。本研究在体外和体内模型中评估MET对溴酸钾(KBrO3)诱导的肝毒性的保护作用。将肝细胞暴露于含或不含二甲双胍(20、40和60µM)的KBrO3中,评估细胞活力和活性氧水平。在体内,将大鼠分为5组:对照组、KBrO3组和二甲双胍组(25、50和100 mg/kg)。分析肝脏和血液样本的组织学变化、氧化应激标志物、脂质过氧化、肝酶和PI3K/Akt信号。结果skbro3暴露显著降低细胞活力,升高ROS水平。与MET剂量依赖的共处理可恢复细胞活力,60µM MET可达到约80%的活力。二甲双胍也降低了ROS水平,高浓度时平均荧光强度接近控制值。在体内研究中,KBrO3暴露会升高脂质过氧化标志物,降低抗氧化酶活性,引发氧化应激和炎症。二甲双胍可显著减轻组织学肝损伤,抑制促炎细胞因子,增强抗氧化酶活性,调节PI3K/Akt信号通路,促进细胞存活,减轻氧化损伤。结论二甲双胍通过提高细胞活力和降低活性氧水平,有效保护肝细胞免受kbro3诱导的细胞毒性。二甲双胍通过降低氧化应激、调节炎症通路(NF-kB)和调节PI3K/Akt信号级联,成功减轻了kbro3诱导的肝损伤,为其肝保护作用提供了分子证据。引用方式:马斌,郑生,谢宁,等。二甲双胍通过减弱NF-kB和PI3K/Akt通路减轻溴酸钾诱导的大鼠肝脏不适。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.03.002。
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引用次数: 0
Octoploid blueberry development for drought tolerance: A combined approach of in vitro polyploidization and somatic organogenesis 八倍体蓝莓的抗旱发育:体外多倍体和体细胞器官发生相结合的方法
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-05-01 Epub Date: 2025-03-31 DOI: 10.1016/j.ejbt.2025.01.004
Alejandra Araujo Heraldez , Susana Valdez Peñuelas , Gabriela Jarpa-Tauler , Aparna Banerjee , Kattia Núñez-Montero , Patricio Arce-Johnson , Jesús L. Romero-Romero

Background

The blueberry (Vaccinium spp.) is a fruit commercially known for its high quality and health benefits, particularly for its bioactive antioxidant compounds, which are important in the medical field. However, factors such as genotype, stage of fruit ripening and environmental conditions impact the biosynthesis of bioactive compounds in the berry, as well as their yield and cultivation costs. In Mexico, particularly in the state of Sinaloa, extreme climatic conditions limit the cultivation of blueberry and highlight the need for the development of new varieties with low chilling requirements and tolerance to drought conditions.

Results

Through the combined use of somatic organogenesis and in vitro polyploidization, genetic variability was promoted in the commercial blueberry plant variety “Biloxi”. To achieve this purpose, blueberry microcuttings were treated with colchicine (0.02%) for six hours for 2, 4, 6 and 8 consecutive days and induced to form shoots in vitro with Zeatin (1 mg·L−1). Out of 304 generated plants, 36 showed lower stomatal density and 9 lines showed higher stomatal density. Likewise, 5 and 49 lines presented lower and larger stomatal sizes, respectively. In 9 lines, a higher chlorophyll content was found (10% to 200%) compared to the control treatment. Ploidy analysis using flow cytometry showed the successful generation of four octoploid blueberry plants.

Conclusions

This work successfully generated new octoploid blueberry plants. Currently, all the lines that presented histological, biochemical and/or genetic modifications are being evaluated under greenhouse conditions for fruit quality and drought tolerance.
How to cite: Heraldez AA, Peñuelas SV, Jarpa-Tauler G, et al. Octoploid blueberry development for drought tolerance: A combined approach of in vitro polyploidization and somatic organogenesis. Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.004.
蓝莓(Vaccinium spp.)是一种以其高品质和健康益处而闻名的水果,特别是其生物活性抗氧化化合物,这在医学领域很重要。然而,基因型、果实成熟阶段和环境条件等因素影响着浆果中生物活性化合物的生物合成,以及它们的产量和栽培成本。在墨西哥,特别是在锡那罗亚州,极端的气候条件限制了蓝莓的种植,并突出了开发低低温要求和耐旱条件的新品种的必要性。结果通过体细胞器官发生和离体多倍体分化相结合的方法,促进了蓝莓商品品种“碧露”的遗传变异。为达到这一目的,用0.02%秋水仙碱连续2、4、6和8天处理蓝莓微扦插6小时,用玉米素(1 mg·L−1)诱导其离体成芽。304株植株中气孔密度较低的有36株,气孔密度较高的有9株。同样,5号系和49号系的气孔大小也分别较小和较大。其中9个品系的叶绿素含量高于对照处理(10% ~ 200%)。利用流式细胞术进行倍性分析,结果表明成功获得了4株八倍体蓝莓植株。结论成功地获得了八倍体蓝莓新植株。目前,所有表现出组织学、生化和/或遗传修饰的品系正在温室条件下进行果实品质和耐旱性评价。引用方式:Heraldez AA, Peñuelas SV, Jarpa-Tauler G,等。八倍体蓝莓的抗旱发育:体外多倍体和体细胞器官发生相结合的方法。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.01.004。
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引用次数: 0
Novel Erodium glaucophyllum (L.) Aiton growing in arid environment: Phytochemical characterization, antimicrobial, antioxidant, and anticancer potential 新青花紫荆(L.)干旱环境下生长的艾草:植物化学特性、抗菌、抗氧化和抗癌潜力
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-03 DOI: 10.1016/j.ejbt.2025.01.005
Amr H. Hashem , Bahaa M. Badr , Fathy M. Elkady , Mostafa A. Abdel-Maksoud , Abdulaziz Alamri , Mohamed A. El-Tayeb , Bushra H. Kiani , Amer M. Abdelaziz

Background

The misuse of antimicrobial agents resulted in a global serious health concern, namely antimicrobial resistance. Also, traditional bioactive compounds are associated with undesirable adverse effects. This study aimed to first assess the phytochemical analyses and biological activities of Erodium glaucophyllum (L.) Aiton from the arid region.

Results

The gas chromatography-mass spectroscopy analysis of Erodium glaucophyllum leaves crude extract revealed the presence of 36 biologically vital compounds, with 8 main compounds being identified. Docosenamide, hexadecanoic acid, thiocarbamic acid, hentriacontane, β-sitosterol, quinoline, and oleic acid were among the most significant compounds. Docosenamide was the most prevalent compound, comprising 45.3%. The phytochemical analysis revealed the presence of a diverse array of chemical compounds, such as carbohydrates, polyphenols, flavonoids, and tannins. In moderate concentrations, saponins, glycosides, quinones, proteins, and amino acids were present. Additionally, alkaloids, steroids, diterpenes, and cardiac glycosides were identified in trace amounts. Also, chlorogenic acid was the dominant with 69.14% among other phenolic compounds. The antimicrobial results of the tested extract showed promising activity against Bacillus subtilis, Staphylococcus aureus, Salmonella typhimurium, and Pseudomonas aeruginosa, with minimum inhibitory concentration of 31.25, 15.62, 15.62, and 62.5 µg/ml, respectively. Furthermore, the extract demonstrated potent antioxidant activity, with an EC50 of 51.7 µg/ml, and anticancer activity against MCF-7 malignant cell line, with an IC50 of 58.4 µg/ml.

Conclusions

The tested crude extract of Erodium glaucophyllum leaves represents a potential source of bioactive compounds that possess antimicrobial, antioxidant, and anticancer properties.
How to cite: Hashem AH, Badr BM, Elkady FM, et al. Novel Erodium glaucophyllum (L.) Aiton growing in arid environment: Phytochemical characterization, antimicrobial, antioxidant, and anticancer potential. Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.005.
抗菌药物的滥用导致了全球严重的健康问题,即抗菌药物耐药性。此外,传统的生物活性化合物与不良反应有关。本文首先对青花Erodium glaucophyllum (L.)的植物化学分析和生物活性进行了初步研究。来自干旱地区的艾顿。结果通过气相色谱-质谱联用分析,鉴定出36种生物活性化合物,鉴定出8种主要化合物。二十二酰胺、十六烷酸、硫代氨基甲酸、三康烷、β-谷甾醇、喹啉和油酸是最显著的化合物。Docosenamide是最常见的化合物,占45.3%。植物化学分析揭示了多种化合物的存在,如碳水化合物、多酚、类黄酮和单宁。在中等浓度,皂苷,糖苷,醌,蛋白质和氨基酸存在。此外,生物碱、类固醇、二萜和心脏苷被鉴定出微量。绿原酸在其他酚类化合物中占主导地位,占69.14%。对枯草芽孢杆菌、金黄色葡萄球菌、鼠伤寒沙门菌和铜绿假单胞菌的抑菌活性较好,最低抑菌浓度分别为31.25、15.62、15.62和62.5µg/ml。此外,提取物显示出强大的抗氧化活性,其EC50为51.7µg/ml,对MCF-7恶性细胞系的抗癌活性,其IC50为58.4µg/ml。结论青花Erodium glaucophyllum叶片粗提物具有抗菌、抗氧化和抗癌活性。如何引用:Hashem AH, Badr BM, Elkady FM等。新青花紫荆(L.)干旱环境下生长的艾草:植物化学特性、抗菌、抗氧化和抗癌潜力。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.01.005。
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引用次数: 0
Efficient production of 6-hydroxynicotinic acid by newly isolated Pseudomonas poae 新分离的poae假单胞菌高效生产6-羟基烟酸
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-05-01 Epub Date: 2025-03-14 DOI: 10.1016/j.ejbt.2025.01.002
Yi Li , Jiacheng Tang , Kaixiang Xin , Zongda Chen , Lele Zhao , Yifan Zhao , Yinbiao Xu , Pei Zhou , Yang Sun , Yupeng Liu , Hua Li

Background

Nicotinic acid dehydrogenase possesses the capability to convert nicotinic acid into 6-hydroxynicotinic acid, a compound of significant research value as a pharmaceutical intermediate. The extraction of nicotinic acid dehydrogenase is primarily performed by strains. However, the enzyme activity of the strains reported currently is relatively low, and their potential to catalyze the production of 6-hydroxynicotinic acid is insufficient to meet industrial requirements.

Results

Due to the revealing properties of 6-hydroxynicotinic acid, this study proposes a technique for calculating the luminescence intensity of colonies, which is based on a fluorescence spectrometer. The developed method establishes a reliable linear relationship (88.2%) between the luminescence intensity and enzyme activity. Consequently, it has been employed to screen strains that produce nicotinate dehydrogenase. This screening approach allows for the evaluation of about 500 enzyme-producing strains daily, presenting an efficient strategy for screening.

Conclusions

Through this approach, a novel high enzyme activity strain producing nicotinic acid dehydrogenase, Pseudomonas poae have been obtained, which is designated as HD530. After process optimization, it was utilized to produce 6-hydroxynicotinic acid, achieving a high yield of 155.45 g/L within 72 h, meeting the requirements for industrial production. The effectiveness and potential of this technique lie in its application for strain screening and improvement.
How to cite: Li Y, Tang J, Xin K, et al. Efficient production of 6-hydroxynicotinic acid by newly isolated Pseudomonas poae. Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.002.
烟酸脱氢酶具有将烟酸转化为6-羟基烟酸的能力,6-羟基烟酸是一种具有重要研究价值的医药中间体。烟酸脱氢酶的提取主要通过菌株进行。然而,目前报道的菌株的酶活性相对较低,催化生产6-羟基烟酸的潜力不足以满足工业要求。结果由于6-羟基烟酸具有揭示性,本研究提出了一种基于荧光光谱仪计算菌落发光强度的方法。该方法在发光强度与酶活性之间建立了可靠的线性关系(88.2%)。因此,它已被用于筛选菌株产生烟酸脱氢酶。这种筛选方法允许每天评估约500种产酶菌株,提出了一种有效的筛选策略。结论通过该方法获得了一株产烟酸脱氢酶的新型高酶活性菌株,命名为HD530。经工艺优化后,利用该工艺生产6-羟基烟酸,72 h产率达到155.45 g/L,满足工业生产要求。该技术的有效性和潜力在于其在菌株筛选和改良方面的应用。引用方式:李颖,唐杰,辛凯,等。新分离的poae假单胞菌高效生产6-羟基烟酸。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.01.002。
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引用次数: 0
Optimizing conditions for augmented production of amylase by Talaromyces islandicus AUMC 11391 岛Talaromyces islandicus AUMC 11391提高淀粉酶产量的条件优化
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-08 DOI: 10.1016/j.ejbt.2025.01.008
Osama A.M. Al-Bedak , Ahmed M. Moharram , Fuad Ameen , Steven L. Stephenson , Marwa M.M. Idres , Manal M. Yasser

Background

To satisfy rising biotechnological needs, climate change, and depleting water supplies, amylases that can survive high temperatures, and salt concentrations must be developed. Amylases are the most important enzymes that comprise approximately 25–33% of the international enzyme market and have a great role in many industries.

Results

In this investigation, Talaromyces islandicus AUMC 11391 was used to produce amylase in submerged fermentation (SmF) in an augmented concentration of 232 ± 36 U/mL after 8 d of incubation at pH 6.0 and 30°C using sodium nitrate as a nitrogen supply. The obtained enzyme was partly purified employing 70% ammonium sulfate and then dialysis. The activity of the produced amylase exhibited reached the peak (992.14 ± 80 U/mg protein) at pH 5.0 and 55°C. Cu, Co, Fe, Ni, Ca, and Zn had an activating effect on the activity of the amylase enzyme at pH 5.0 and 55°C by 134.57, 123.1, 115.4, 109.76, 105.43, and 103.2%, respectively. The Km and Vmax were recorded as 132.1 mM and 60.6 µmol/min, respectively. T. islandicus AUMC 11391′s-amylase hydrolyzed the raw starch of maize, sorghum, wheat, rice, and oat at rates of 12.3, 113.7, 32.25, 34.67, and 73.6% in contrast to the soluble starch.

Conclusions

This enhanced α-amylase from T. islandicus AUMC 11391 looks to be a potential option to meet the present amylase requirements of a variety of industrial processes because of its improved production and beneficial properties.
How to cite: Al - Bedak O.A.M., Moharram AM., Ameen F, et al. Optimizing conditions for augmented production of amylase by Talaromyces islandicus AUMC 11391. Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.008.
为了满足不断增长的生物技术需求、气候变化和耗竭的水供应,必须开发能够在高温和盐浓度下生存的淀粉酶。淀粉酶是最重要的酶,约占国际酶市场的25-33%,在许多工业中发挥着重要作用。结果在pH 6.0、30℃条件下,以硝酸钠为供氮源,培养8 d后,利用岛Talaromyces islandicus AUMC 11391在增加浓度为232±36 U/mL的条件下产生淀粉酶。所得酶用70%硫酸铵进行部分纯化,然后透析。在pH 5.0和55℃条件下,淀粉酶活性达到峰值(992.14±80 U/mg蛋白)。Cu、Co、Fe、Ni、Ca和Zn在pH 5.0和55°C条件下对淀粉酶活性的激活作用分别为134.57、123.1、115.4、109.76、105.43和103.2%。Km和Vmax分别为132.1 mM和60.6µmol/min。岛霉AUMC 11391 s-淀粉酶对玉米、高粱、小麦、水稻和燕麦原料淀粉的水解率分别为12.3%、113.7%、32.25%、34.67%和73.6%。结论从岛霉AUMC 11391中提取的α-淀粉酶具有提高产量和有益性能的优点,有望满足目前多种工业工艺对淀粉酶的需求。如何引用:Al - Bedak o.a.m., Moharram a.m.。, Ameen F,等。岛Talaromyces islandicus AUMC 11391提高淀粉酶产量的条件优化。中国生物医学工程学报(英文版);2009;16。https://doi.org/10.1016/j.ejbt.2025.01.008。
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引用次数: 0
Selection and validation of stable reference genes in guava (Psidium guajava L.) for reliable and consistent gene expression analysis 番石榴(Psidium guajava L.)稳定内参基因的选择和验证,以获得可靠和一致的基因表达分析
IF 2.3 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pub Date : 2025-05-01 Epub Date: 2025-04-04 DOI: 10.1016/j.ejbt.2025.01.006
Sandeep Kumar , Manoharan Muthukumar , Anju Bajpai , Amar Kant Kushwaha , Israr Ahmad , Yashi Bajpai , Anshuman Singh , Thukkaram Damodaran , Mala Trivedi

Background

Ideal stably expressing housekeeping gene to be used as internal control needs to be optimized for efficient gene expression analysis for accurate mRNA quantitation. In pursuit of identifying suitable reference genes for gene expression analysis in guava, a systematic study was conducted using different tissues of guava cv. Allahabad Safeda examining 10 housekeeping genes such as Actin (PgACT), Elongation factor 1G (PgEF1G), Elongation factor 2 (PgEF2), Tubulin (PgTUB1), Elongation factor 1 α (PgEF1a), Monensin sensitivity1 (PgMON1), Histone H3 (PgH3), RNA-binding protein 47 (PgRBP47), Polyubiquitin_X1 (PgPOLX1), and Polyubiquitin_X2 (PgPOLX2).

Results

qRT-PCR analysis showed amplification efficiencies ranging from 74.4% to 124.9%, with correlation coefficients exceeding 0.98. The stability of these genes’ expression was evaluated using six methods: GeNorm, NormFinder, BestKeeper, RefFinder, comparative delta-Ct, and Stability index in which different methods identified PgRBP47 as least stable and indicated its unsuitability as a reference gene but showed variations in the ranking of the genes for gene stability.

Conclusions

Comparison of all the methods and accounting for the top 3 ranks of gene stability, three genes i.e., PgTUB1, PgEF1a, and PgEF2 were identified as more stable housekeeping genes across different tissues of guava and could be considered as ideal reference genes for normalization in gene expression studies of guava.
How to cite: Kumar S, Muthukumar M, Bajpai A, et al. Selection and validation of stable reference genes in guava (Psidium guajava L.) for reliable and consistent gene expression analysis. Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.006.
背景为了进行高效的基因表达分析,准确定量 mRNA,需要优化理想的稳定表达的管家基因作为内对照。为了确定适合番石榴基因表达分析的参考基因,研究人员利用番石榴品种 Allahabad Safeda 的不同组织进行了一项系统研究。研究人员利用 Allahabad Safeda 番石榴品种的不同组织进行了系统研究,检测了 10 个看家基因,如肌动蛋白(PgACT)、伸长因子 1G(PgEF1G)、伸长因子 2(PgEF2)、微管蛋白(PgTUB1)、延长因子 1 α (PgEF1a)、莫能菌素敏感性 1 (PgMON1)、组蛋白 H3 (PgH3)、RNA 结合蛋白 47 (PgRBP47)、多泛素_X1 (PgPOLX1) 和多泛素_X2 (PgPOLX2)。结果qRT-PCR分析显示扩增效率从74.4%到124.9%不等,相关系数超过0.98。使用六种方法评估了这些基因表达的稳定性:不同的方法将 PgRBP47 鉴定为最不稳定的基因,并指出其不适合作为参考基因,但在基因稳定性的排名上显示出差异、PgTUB1、PgEF1a 和 PgEF2 是番石榴不同组织中较稳定的看家基因,可作为番石榴基因表达研究中理想的归一化参考基因:Kumar S, Muthukumar M, Bajpai A, et al. 在番石榴(Psidium guajava L.)中选择和验证稳定的参考基因以进行可靠一致的基因表达分析。Electron J Biotechnol 2025;75. https://doi.org/10.1016/j.ejbt.2025.01.006.
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引用次数: 0
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Electronic Journal of Biotechnology
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