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涡轮溶解法:一种用于细胞裂解的低成本、小体积的商业珠磨仪替代方法。

Turbolysis: A low-cost, small footprint alternative to commercial bead beaters for cell lysis.

作者信息

Limberis Jason D, Metcalfe John Z

机构信息

Division of Pulmonary and Critical Care Medicine, Zuckerberg San Francisco General Hospital and Trauma Centre, University of California, San Francisco, San Francisco, CA, USA.

出版信息

HardwareX. 2024 Aug 27;19:e00576. doi: 10.1016/j.ohx.2024.e00576. eCollection 2024 Sep.

DOI:10.1016/j.ohx.2024.e00576
PMID:39280234
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11402052/
Abstract

turboLysis is a novel mechanical cell lysis device that utilizes small beads to efficiently lyse tough cells like Mycobacterium, Saccharomyces, and Arabidopsis. We compared turboLysis to bead beating using the BeadBug 6 for several concentrations of roughly correlated to the bacterial load commonly seen in patient samples. turboLysis performed similarly to the BeadBug at low bacterial concentrations and outperformed it at high concentrations above 2x10 CFU/ml (p < 0.005). Thus, turboLysis offers good cell lytic performance in a small form factor at a low cost.

摘要

TurboLysis是一种新型的机械细胞裂解装置,它利用小珠子有效地裂解诸如分枝杆菌、酿酒酵母和拟南芥等坚韧的细胞。我们使用BeadBug 6针对几种浓度(大致与患者样本中常见的细菌载量相关)将TurboLysis与珠磨法进行了比较。在低细菌浓度下,TurboLysis的表现与BeadBug相似,而在高于2×10 CFU/ml的高浓度下,其表现优于BeadBug(p < 0.005)。因此,TurboLysis以低成本提供了小尺寸的良好细胞裂解性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/4c87a8e0b352/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/199e9f0065fb/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/36f94e8bf07d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/4c87a8e0b352/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/199e9f0065fb/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/36f94e8bf07d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9a/11402052/4c87a8e0b352/gr2.jpg

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本文引用的文献

1
DNA Thermo-Protection Facilitates Whole-Genome Sequencing of Mycobacteria Direct from Clinical Samples.DNA热保护有助于直接从临床样本中对分枝杆菌进行全基因组测序。
J Clin Microbiol. 2020 Sep 22;58(10). doi: 10.1128/JCM.00670-20.
2
Direct Whole-Genome Sequencing of Sputum Accurately Identifies Drug-Resistant Mycobacterium tuberculosis Faster than MGIT Culture Sequencing.直接全基因组测序痰液比 MGIT 培养测序更准确地鉴定耐药结核分枝杆菌。
J Clin Microbiol. 2018 Jul 26;56(8). doi: 10.1128/JCM.00666-18. Print 2018 Aug.
3
Optimized method for preparation of DNA from pathogenic and environmental mycobacteria.
从致病性和环境分枝杆菌中制备DNA的优化方法。
Appl Environ Microbiol. 2009 Jan;75(2):414-8. doi: 10.1128/AEM.01358-08. Epub 2008 Dec 1.