Halothermophilic Cas9 and dCas9 Interaction with Variety sgRNA In-silico

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Kenny Lischer, Kholisoh Hayatia, Muhammad Hayka Fabianl, Fina Amreta Laksmi, Yudhi Nugraha, Hamdan Dwi Rizqi, Riri Fauziyya, Sarmoko, Mohd Shukuri Mohamad Ali

2025 International Journal of Technology Vol. 16 Issue 1 Article Cited by 0 SDG 14SDG 17 Quartile

Abstract

Industrial bioprocesses often require microorganisms that can adapt to specific conditions, such as halothermophilic bacteria capable of producing biosurfactants with various applications. Enhancing production yield is important, and one approach genetic modification. Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) is a highly effective method for genetic editing; however, its use in halothermophilic bacteria remains limited. So far, optimal genetic editing with Cas9 has only been achieved in thermophilic bacteria unsuitable for high-salt environments. For determining optimal CRISPR involves analyzing the binding interaction between sgRNA (single guide RNA) and Cas9 using Molecular Docking in halothermophilic bacteria. This includes preparing the structures of Cas9 and sgRNA, simulating them with HDOCK software, and data analysis. Molecular Docking has advantages such as cost-effectiveness and time efficiency in designing the optimal sgRNA length. Optimization of sgRNA is achieved by varying the lengths of repeat, spacer, and tracrRNA, aiming for the lowest binding energy values and visually feasible designs. For Cas9 from the selected bacterium, Klebsiella pneumoniae, the optimal sgRNA design for Cas9 involves a spacer of 10 nt. In contrast, dCas9 involves a spacer of 10 nt, a repeat of 36 nt, and tracrRNA of 63 nt. The native temperature of the bacteria did not significantly affect the optimal sgRNA length. © (2025), (Faculty of Engineering, Universitas Indonesia). All Rights Reserved.

Affiliations

Bioprocess Engineering, Department of Chemical Engineering, Faculty of Engineering, Universitas Indonesia, West Java, Depok, 16424, Indonesia; Research Centre of Biomedical Engineering, Department of Chemical Engineering, Faculty of Engineering, Universitas Indonesia, West Java, Depok, 16424, Indonesia; Chemical Engineering, Department of Chemical Engineering, Faculty of Engineering, Universitas Indonesia, West Java, Depok, 16424, Indonesia; National Research and Innovation Agency, West Java, Cibinong, 16915, Indonesia; Research Center for Molecular Biology Eijkman BRIN, National Research and Innovation Agency, West Java, Cibinong, 16915, Indonesia; Department of Molecular Medicine, University of Pavia, Pavia, 27100, Italy; Department of Chemistry, Faculty of Science and Data Analytics, Institut Teknologi Sepuluh Nopember, Jawa Timur, Surabaya, 60111, Indonesia; Department of Pharmacy, Sumatera Institute of Technology, Lampung, 35365, Indonesia; Enzyme and Microbial Technology Research Center, Universiti Putra Malaysia, Selangor, Serdang, 43400, Malaysia

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