Effect of Proteinase-K on Genomic DNA Extraction from Gram-positive Strains

M. Shahriar, R. Haque, Shaila Kabir, Irin Dewan, M. A. Bhuyian
{"title":"Effect of Proteinase-K on Genomic DNA Extraction from Gram-positive Strains","authors":"M. Shahriar, R. Haque, Shaila Kabir, Irin Dewan, M. A. Bhuyian","doi":"10.3329/SJPS.V4I1.8867","DOIUrl":null,"url":null,"abstract":"Direct extraction of DNA from natural environment and clinical samples has become a useful alternative for the phylogenetic identification and in situ detection of individual microbial cells without cultivation. In this study, three different Gram positive microorganisms ( B. cereus, B. subtilis, and S. aureus ) were chosen for genomic DNA extraction. High salt SDS (Sodium Dodesyl Sulfate) based extraction method was followed to extract genomic DNA with addition of three different lysis protocols to observe the effect of proteinase-K on total genomic DNA yield, lysis steps were carried with SDS, SDS with 3 μl proteinase-K and SDS with 6μl proteinase-K. High molecular weight intact DNA bands were observed only for Bacillus subtilis when the extraction procedure was carried out in presence of SDS, SDS with proteinase-K (3μl) and SDS with increased amount of proteinase-K (6μl). In presence of SDS and increased amount of proteinase-K (6μl) the mean value of DNA concentration for Bacillus cereus , Bacillus subtilis , and Staphylococcus aureus were found to be 1.53±0.15, 1.36±0.10 and 1.65±0.10 μg/μl respectively. However, in absence of proteinase-K, the mean values of DNA concentration were found to be decreased (1.28±0.10, 1.34±0.15, 1.23±0.10 μg/μl for B. cereus, B. subtilis , and S. aureus respectively) for all these stains. Although in case of B. subtilis the overall effect of proteinase-K was not found to be significant in terms of DNA concentration and DNA band intensity, however, for B. cereus , and S. aureus sharp decrease in total extracted DNA concentration was observed suggesting the increased lysis effect of proteinase-K on the thick peptidoglycan layer of Gram-positive cell wall such as B. cereus , and S. aureus . Key words : Extraction; Genomic DNA; Lysis buffer; Gram positive organism. DOI: http://dx.doi.org/10.3329/sjps.v4i1.8867 SJPS 2011; 4(1): 53-57","PeriodicalId":21823,"journal":{"name":"Stamford Journal of Pharmaceutical Sciences","volume":"29 1","pages":"53-57"},"PeriodicalIF":0.0000,"publicationDate":"2011-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"28","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stamford Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/SJPS.V4I1.8867","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 28

Abstract

Direct extraction of DNA from natural environment and clinical samples has become a useful alternative for the phylogenetic identification and in situ detection of individual microbial cells without cultivation. In this study, three different Gram positive microorganisms ( B. cereus, B. subtilis, and S. aureus ) were chosen for genomic DNA extraction. High salt SDS (Sodium Dodesyl Sulfate) based extraction method was followed to extract genomic DNA with addition of three different lysis protocols to observe the effect of proteinase-K on total genomic DNA yield, lysis steps were carried with SDS, SDS with 3 μl proteinase-K and SDS with 6μl proteinase-K. High molecular weight intact DNA bands were observed only for Bacillus subtilis when the extraction procedure was carried out in presence of SDS, SDS with proteinase-K (3μl) and SDS with increased amount of proteinase-K (6μl). In presence of SDS and increased amount of proteinase-K (6μl) the mean value of DNA concentration for Bacillus cereus , Bacillus subtilis , and Staphylococcus aureus were found to be 1.53±0.15, 1.36±0.10 and 1.65±0.10 μg/μl respectively. However, in absence of proteinase-K, the mean values of DNA concentration were found to be decreased (1.28±0.10, 1.34±0.15, 1.23±0.10 μg/μl for B. cereus, B. subtilis , and S. aureus respectively) for all these stains. Although in case of B. subtilis the overall effect of proteinase-K was not found to be significant in terms of DNA concentration and DNA band intensity, however, for B. cereus , and S. aureus sharp decrease in total extracted DNA concentration was observed suggesting the increased lysis effect of proteinase-K on the thick peptidoglycan layer of Gram-positive cell wall such as B. cereus , and S. aureus . Key words : Extraction; Genomic DNA; Lysis buffer; Gram positive organism. DOI: http://dx.doi.org/10.3329/sjps.v4i1.8867 SJPS 2011; 4(1): 53-57
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
蛋白酶k对革兰氏阳性菌株基因组DNA提取的影响
直接从自然环境和临床样本中提取DNA已成为一种有用的替代方法,用于系统发育鉴定和原位检测单个微生物细胞而无需培养。本研究选取三种不同的革兰氏阳性微生物(蜡样芽孢杆菌、枯草芽孢杆菌和金黄色葡萄球菌)进行基因组DNA提取。采用高盐SDS(十二烷基硫酸钠)提取方法提取基因组DNA,并添加三种不同的裂解方案,观察蛋白酶- k对基因组DNA总产率的影响,裂解步骤分别用SDS、3 μl蛋白酶- k SDS和6μl蛋白酶- k SDS进行。在SDS、添加蛋白酶k (3μl)的SDS和添加蛋白酶k (6μl)的SDS的条件下,只有枯草芽孢杆菌的DNA条带具有较高的分子量。在添加SDS和增加蛋白酶k量(6μl)的情况下,蜡样芽孢杆菌、枯草芽孢杆菌和金黄色葡萄球菌的DNA浓度平均值分别为1.53±0.15、1.36±0.10和1.65±0.10 μl。然而,在缺乏蛋白酶k的情况下,所有菌株的DNA浓度平均值均降低(蜡样芽孢杆菌、枯草芽孢杆菌和金黄色葡萄球菌的DNA浓度平均值分别为1.28±0.10、1.34±0.15、1.23±0.10 μl)。虽然在枯草芽孢杆菌中,蛋白酶- k对DNA浓度和DNA条带强度的总体影响不显著,但在蜡样芽孢杆菌和金黄色葡萄球菌中,总提取DNA浓度急剧下降,提示蛋白酶- k对蜡样芽孢杆菌和金黄色葡萄球菌等革兰氏阳性细胞壁厚肽聚糖层的裂解作用增强。关键词:萃取;基因组DNA;裂解缓冲;革兰氏阳性有机体。DOI: http://dx.doi.org/10.3329/sjps.v4i1.8867 SJPS 2011;4 (1): 53-57
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Dissolution study of Spironolactone by using solid dispersion technique Toxicological studies of Darvyadi Kvatha Curna using albino rats In-vitro phytochemical and anthelmintic activity of Cocculus hirsutus Linn. and Rumex dentatus Linn. Risk factors and trends of common cancers in Bangladesh: Outcome of hospital based case control survey conducted in Dhaka city, Bangladesh Preparation and comparative evaluation of liquisolid compacts and solid dispersions of Valsartan
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1