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Secalonic Acid and Benzoic Acid Analogues Exhibiting Cyto toxicity against Cancer Cells Isolated from Claviceps yanagawaensis 二卡隆酸和苯甲酸类似物对柳条锁骨癌细胞具有细胞毒性
Pub Date : 2022-01-01 DOI: 10.4236/aim.2022.1212045
Yuji Doi, Daigo Wakana, S. Kitaoka, Hisashi Takeda, E. Tanaka, T. Hosoe
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引用次数: 1
SARS-CoV-2 Infection Is Associated with Vitamin D Deficiency in Côte d’Ivoire 在Côte科特迪瓦,SARS-CoV-2感染与维生素D缺乏有关
Pub Date : 2022-01-01 DOI: 10.4236/aim.2022.122004
L. Boyvin, Y. G. Yayé, Gnogbo Alexis Bahi, Aya Jeanne Armande Aké, K. Séri, D. Sévédé, S. Eholie, M. Dosso, A. Djaman
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引用次数: 0
Research status and prospect of the antibacterial effect of equol 马雌酚抗菌作用的研究现状与展望
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.114024
奥 孙
Equol, is a kind of phytoestrogenic compound, which synthesized by soybean isoflavones by intestinal microbiota. It has high affinity for estrogen receptor and higher biological activity than soybean isoflavones, so it is one of the widely studied small molecule substances. Equol has many biological effects, such as hormone like effect, antioxidation, immune regulation, etc. In this paper, the biological activity and antibacterial effect of equol were reviewed, in order to provide new ideas for the antibacterial treatment of equol.
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引用次数: 0
Summary and Prospect of Microbial Degradation of Roxarsone 洛克沙酮微生物降解研究综述与展望
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.114028
祯 王
Present, Roxarsone is the most economical organic arsenarsone preparation, which is widely used in the breeding industry as a feed additive. However, due to the low absorption and conversion efficiency of Roxarsone in livestock and poultry, a large amount of Roxarsone flows into the external environment along with excrement. Simple composting and conventional sewage treatment can‘t be completely removed, but discharged into water and soil, resulting in arsenic compound pollution. In addition, microorganisms or light in the environment can degrade Roxarsone into a variety of arsenic compounds, such as 4-hydroxy-3-aminobenzene arsenic acid (HAPA), which can cause serious harm to the environment and human body. At present, in addition to physical and chemical methods, microbial method also has a good degradation effect of Roxarsone. This paper reviewed the research progress on the non-biodegradation and biodegradation transformation of Roxarsone and its related products. The main conclusions are: the non-biodegradation and bio-degradation transformation of Roxarsone is greatly affected by environmental factors, and it is easy to produce more toxic pollutants. Biodegradation and transformation: the irreplaceable role of microorganisms is mainly reflected in: (1) Microbial adsorption and accumulation, including reversible and irreversible processes; (2) Bacterial degradation of Roxarsone; (3) Degradation of Roxarsone by fungi; (4) Degradation of Roxarsone by yeast. Finally, the prospect of applying microbial method to Roxarsone pollution remediation was discussed.
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引用次数: 0
Amplification of Fluorescent Cy5DNA and Separation-Detection of Digestion Product Cy5DNA荧光扩增及消化产物分离检测
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.114030
园霞 郑
[Objective] Amplified with dNTPs added with a specific ratio of fluorescent Cy5-dATP, fluorescent Cy5DNA can assay exonuclease such as T5 DNA exonuclease (T5exo), key is separation-detection of digestion product. [Method] Amplified with dNTPs added with 1/1000 Cy5-dATP, a 5851 bp fluorescent Cy5DNA pET28a-xyn served for T5exo digestion. Basing on DNA-absorbing principle of DNA-clean column, a 2-flod buffer P3 (2×P3) that of DNA solution was determined as the least quantity of a column to absorb DNA. Next, a DNA-clean column with 2×P3 served to separate a so-lution containing Cy5DNAs or equal amount of Cy5DNAs digested by T5exo to collect filtrate and elute, respectively.[Result] Assayed by a microreader SpectraMax ® i3x, the filtrate and elute from 120 ng Cy5DNAs-T5exo solution had a fluorescence value of 7573 and 0, respectively. The elute and filtrate from 120 ng Cy5DNA solution had a fluorescence value of 5824 and 0, respectively. Assayed by a con-focal microscope, the filtrate from Cy5DNA-T5exo solution exhibited Cy5-dATP fluorescence, while the elute did not. The elute from Cy5DNA solution exhibited Cy5 fluorescence, while the filtrate did not. Both the quantity and the quality assay were in agreement with the principle and usage of DNA-clean column. Additionally, correlation was analyzed for concentration of Cy5DNA and Cy5-dATP with fluorescence intensity. [Conclusion] Cy5DNA pET28a-xyn was amplified successfully, and its T5exo digestion product Cy5-dATP was separated by a DNA-clean column with a 2×P3 buffer. The study provided a basis for fluorescent DNA amplification and usage in as-saying DNA-cutting enzyme.
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引用次数: 0
Isolation, Identification and Screening of Lactic Acid Bacteria with Potential Vaginal Health Care 具有阴道保健潜力的乳酸菌的分离、鉴定和筛选
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.111004
佳琳 江
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引用次数: 0
Discussion on the Treatment of Acne Vulgaris 寻常性痤疮的治疗探讨
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.112010
诗航 唐
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引用次数: 0
Progress on the Infection of Intestinal Protozoa in HIV/AIDS Population HIV/AIDS人群肠道原虫感染研究进展
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.112014
厉雨婷 周
{"title":"Progress on the Infection of Intestinal Protozoa in HIV/AIDS Population","authors":"厉雨婷 周","doi":"10.12677/amb.2022.112014","DOIUrl":"https://doi.org/10.12677/amb.2022.112014","url":null,"abstract":"","PeriodicalId":56408,"journal":{"name":"微生物学(英文)","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"66128369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Research Progress of SARS-CoV-2 Omicron Variant SARS-CoV-2组粒变异的研究进展
Pub Date : 2022-01-01 DOI: 10.12677/amb.2022.112006
康泓 王
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引用次数: 1
Synthetic Biology Construct of Ebola Virus in Bacteria Surrogate Is Stable and Safe for Rapid Detection Studies in a BSL-2 Laboratory Setting 在BSL-2实验室环境中,细菌替代物中埃博拉病毒的合成生物学构建稳定、安全,可用于快速检测研究
Pub Date : 2022-01-01 DOI: 10.4236/aim.2022.121003
N. Esiobu, D. Holmes, Chad T Coarsey, W. Asghar, Bodhi Stone
Rapid detection of virulent pathogens during an outbreak is critical for public health advisories and control of the disease in a population. While many molecular techniques for point of care and clinical diagnosis abound, the US experience with the COVID-19 testing in the early stages of the pandemic underscores the critical importance of determining the appropriate target gene(s) with in-built controls that reliably detect pathogens with high sensitivity and specificity. Assays and research for diagnostics and therapy could be slowed during an epidemic because access to the required BSL-3 and BSL-4 laboratories are limited. So, during the 2014 West Africa Ebola outbreak, we tested the hypothesis that using synthetic cDNA of Ebolavirus in a bacteria surrogate (fit for all lab settings), would remain unmutated and safe after several generations, serving as an effective positive control in research settings, self test and point-of-care detection platforms. Primers were designed for the detection and quantification of the nucleoprotein (NP) gene of the 2014 Makona Ebola strain (KR781608.1, 733 1332 bp). To test the stability of artificially inserted translation arrest in the Orf of the model gene, it was edited to include three STOP codons in the RNA transcript using SNAP GENE. The segment was then spliced into a high copy number plasmid, cloned into One Shot TOP10 Escherichia coli (Invitrogen), and tested for stability and safety by periodic subculture, extraction and sequencing. Unlike COVID-19, rapid detection of blood-borne etiologies like Ebola requires optimized protocols for blood matrix. Using real-time PCR and newly designed primer pairs, the EBOV surrogate was detected and enumerated in human blood and regular broth and buffers. Based on aligned sequence analysis, the EBOV synthetic NP gene was stable (>99.9999% similarity coefficient) for at least 3 months. Detection sensitivity in broth and blood was at least 100 cells/ml or about 5.8 How to cite this paper: Esiobu, N., Holmes, D., Coarsey, C., Asghar, W. and Stone, B. (2022) Synthetic Biology Construct of Ebola Virus in Bacteria Surrogate Is Stable and Safe for Rapid Detection Studies in a BSL-2 Laboratory Setting. Advances in Microbiology, 12, 25-41. https://doi.org/10.4236/aim.2022.121003 Received: November 24, 2021 Accepted: January 25, 2022 Published: January 28, 2022 Copyright © 2022 by author(s) and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/
在疫情期间迅速发现毒性病原体对于公共卫生咨询和在人群中控制疾病至关重要。虽然有许多用于护理点和临床诊断的分子技术,但美国在大流行早期阶段进行COVID-19检测的经验强调了通过内置控制来确定适当的靶基因的重要性,这种内置控制能够可靠地检测出具有高灵敏度和特异性的病原体。在流行病期间,用于诊断和治疗的检测和研究可能会放缓,因为获得所需的生物安全标准3和生物安全标准4实验室的机会有限。因此,在2014年西非埃博拉疫情期间,我们检验了在细菌替代物(适用于所有实验室环境)中使用埃博拉病毒合成cDNA的假设,在几代后仍将保持不变和安全,在研究环境、自我测试和护理点检测平台中作为有效的阳性对照。设计引物用于2014年Makona埃博拉病毒株(KR781608.1, 733 1332 bp)核蛋白(NP)基因的检测和定量。为了测试在模型基因的Orf中人工插入翻译抑制的稳定性,使用SNAP gene编辑RNA转录本,在转录本中包含三个STOP密码子。将该片段剪接到高拷贝数质粒中,克隆到One Shot TOP10大肠杆菌(Invitrogen)中,通过定期传代、提取和测序检测其稳定性和安全性。与COVID-19不同,埃博拉等血源性病因的快速检测需要优化血液基质方案。采用实时荧光定量PCR和新设计的引物对,在人血、普通肉汤和缓冲液中检测和枚举EBOV代物。比对序列分析表明,EBOV合成NP基因至少稳定3个月(相似系数为bb0 99.9999%)。在高汤和血液中的检测灵敏度至少为100个细胞/ml或约5.8。本文引用方式:Esiobu, N., Holmes, D., Coarsey, C., Asghar, W. and Stone, B.(2022)在BSL-2实验室环境中,细菌替代物中的埃博拉病毒合成生物学构建是稳定和安全的快速检测研究。微生物学进展,12,25-41。https://doi.org/10.4236/aim.2022.121003收稿日期:2021年11月24日收稿日期:2022年1月25日出版日期:2022年1月28日版权所有©2022 by作者和Scientific Research Publishing Inc。本作品采用知识共享署名国际许可协议(CC BY 4.0)。http://creativecommons.org/licenses/by/4.0/
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引用次数: 0
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微生物学(英文)
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