二形真菌DNA的强化提取:探讨芽孢与菌丝的优势。

IF 2.7 4区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ahmad El Khatib, Dalal Sabbagh, Sarah Dimassi, Hadi Akl, Karen El Khoury, Jimmy Bou Saba, Mariline Al Kazzi, Hani Dimassi, Sima Tokajian, Nabil Nemer, Charbel Al Khoury
{"title":"二形真菌DNA的强化提取:探讨芽孢与菌丝的优势。","authors":"Ahmad El Khatib, Dalal Sabbagh, Sarah Dimassi, Hadi Akl, Karen El Khoury, Jimmy Bou Saba, Mariline Al Kazzi, Hani Dimassi, Sima Tokajian, Nabil Nemer, Charbel Al Khoury","doi":"10.1002/bab.2786","DOIUrl":null,"url":null,"abstract":"<p><p>The extraction of high-quality DNA from fungi remains a significant challenge due to the structural complexity and resilience of fungal cell walls. This study presents the first comprehensive comparison of DNA extraction efficiency between blastospores (BS) and mycelial cells (MCs) in dimorphic fungi. We evaluated six DNA extraction procedures and two pre-treatment methods to determine their effectiveness in extracting DNA of high quality and yield from both forms. DNA quantification was performed using absolute RT-qPCR targeting the single-copy γ-Actin gene, with specificity and efficiency validated through standardized protocols. Our results showed that BS consistently yielded higher DNA quantity and quality across all conditions, with a mean antilog DNA copy concentration of 5.03 ± 0.20, compared to 2.51 ± 0.20 for MC. DNA quality was superior in BS, as indicated by significantly better 260/280 and 260/230 ratios (31.5% vs. 7.4% for MC, p value = 0.002). Additionally, BS produced higher molecular weight DNA (10,770.5 base pairs vs. 8139.0 base pairs for MC, p value < 0.001) and exhibited greater long-term stability at both 4°C and -20°C. The results demonstrate that BS serve as a more reliable source of high-quality DNA compared to MC. This finding enhances current methodologies in molecular biology and supports more accurate analyses, particularly in studies involving dimorphic fungi.</p>","PeriodicalId":9274,"journal":{"name":"Biotechnology and applied biochemistry","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhanced DNA Extraction From Dimorphic Fungi: Exploring the Advantages of Blastospores Versus Mycelia.\",\"authors\":\"Ahmad El Khatib, Dalal Sabbagh, Sarah Dimassi, Hadi Akl, Karen El Khoury, Jimmy Bou Saba, Mariline Al Kazzi, Hani Dimassi, Sima Tokajian, Nabil Nemer, Charbel Al Khoury\",\"doi\":\"10.1002/bab.2786\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The extraction of high-quality DNA from fungi remains a significant challenge due to the structural complexity and resilience of fungal cell walls. This study presents the first comprehensive comparison of DNA extraction efficiency between blastospores (BS) and mycelial cells (MCs) in dimorphic fungi. We evaluated six DNA extraction procedures and two pre-treatment methods to determine their effectiveness in extracting DNA of high quality and yield from both forms. DNA quantification was performed using absolute RT-qPCR targeting the single-copy γ-Actin gene, with specificity and efficiency validated through standardized protocols. Our results showed that BS consistently yielded higher DNA quantity and quality across all conditions, with a mean antilog DNA copy concentration of 5.03 ± 0.20, compared to 2.51 ± 0.20 for MC. DNA quality was superior in BS, as indicated by significantly better 260/280 and 260/230 ratios (31.5% vs. 7.4% for MC, p value = 0.002). Additionally, BS produced higher molecular weight DNA (10,770.5 base pairs vs. 8139.0 base pairs for MC, p value < 0.001) and exhibited greater long-term stability at both 4°C and -20°C. The results demonstrate that BS serve as a more reliable source of high-quality DNA compared to MC. This finding enhances current methodologies in molecular biology and supports more accurate analyses, particularly in studies involving dimorphic fungi.</p>\",\"PeriodicalId\":9274,\"journal\":{\"name\":\"Biotechnology and applied biochemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biotechnology and applied biochemistry\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1002/bab.2786\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotechnology and applied biochemistry","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/bab.2786","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

由于真菌细胞壁的结构复杂性和弹性,从真菌中提取高质量的DNA仍然是一个重大挑战。本研究首次全面比较了二形真菌中胚孢子(BS)和菌丝细胞(MCs)的DNA提取效率。我们评估了六种DNA提取方法和两种预处理方法,以确定它们在从两种形式中提取高质量和高产量DNA的有效性。采用针对单拷贝γ-Actin基因的绝对RT-qPCR进行DNA定量,通过标准化方案验证特异性和效率。我们的研究结果表明,在所有条件下,BS持续产生更高的DNA数量和质量,平均antilog DNA拷贝浓度为5.03±0.20,而MC为2.51±0.20。BS的DNA质量更好,260/280和260/230的比率明显更好(31.5%比7.4%,p值= 0.002)。此外,BS产生更高分子量的DNA(10,770.5碱基对,而MC为8139.0碱基对,p值)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced DNA Extraction From Dimorphic Fungi: Exploring the Advantages of Blastospores Versus Mycelia.

The extraction of high-quality DNA from fungi remains a significant challenge due to the structural complexity and resilience of fungal cell walls. This study presents the first comprehensive comparison of DNA extraction efficiency between blastospores (BS) and mycelial cells (MCs) in dimorphic fungi. We evaluated six DNA extraction procedures and two pre-treatment methods to determine their effectiveness in extracting DNA of high quality and yield from both forms. DNA quantification was performed using absolute RT-qPCR targeting the single-copy γ-Actin gene, with specificity and efficiency validated through standardized protocols. Our results showed that BS consistently yielded higher DNA quantity and quality across all conditions, with a mean antilog DNA copy concentration of 5.03 ± 0.20, compared to 2.51 ± 0.20 for MC. DNA quality was superior in BS, as indicated by significantly better 260/280 and 260/230 ratios (31.5% vs. 7.4% for MC, p value = 0.002). Additionally, BS produced higher molecular weight DNA (10,770.5 base pairs vs. 8139.0 base pairs for MC, p value < 0.001) and exhibited greater long-term stability at both 4°C and -20°C. The results demonstrate that BS serve as a more reliable source of high-quality DNA compared to MC. This finding enhances current methodologies in molecular biology and supports more accurate analyses, particularly in studies involving dimorphic fungi.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Biotechnology and applied biochemistry
Biotechnology and applied biochemistry 工程技术-生化与分子生物学
CiteScore
6.00
自引率
7.10%
发文量
117
审稿时长
3 months
期刊介绍: Published since 1979, Biotechnology and Applied Biochemistry is dedicated to the rapid publication of high quality, significant research at the interface between life sciences and their technological exploitation. The Editors will consider papers for publication based on their novelty and impact as well as their contribution to the advancement of medical biotechnology and industrial biotechnology, covering cutting-edge research in synthetic biology, systems biology, metabolic engineering, bioengineering, biomaterials, biosensing, and nano-biotechnology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信