Exogenous Production of N-acetylmuramyl-L Alanine Amidase (LysM2) from Siphoviridae Phage Affecting Anti-Gram-Negative Bacteria: Evaluation of Its Structure and Function

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MIRI MORTEZA; Yazdianpour Sepideh; ABOLMAALI SHAMSOZOHA; DARVISH ALIPOUR ASTANEH SHAKIBA

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Journal: Avicenna Journal of Medical Biotechnology Year:2022 | Volume:14 | Issue:1 Page(s): 46-53

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Title

Exogenous Production of N-acetylmuramyl-L Alanine Amidase (LysM2) from Siphoviridae Phage Affecting Anti-Gram-Negative Bacteria: Evaluation of Its Structure and Function

Author(s)

MIRI MORTEZA | Yazdianpour Sepideh | ABOLMAALI SHAMSOZOHA | DARVISH ALIPOUR ASTANEH SHAKIBA | Issue Writer Certificate

Keywords

Antibacterial activity

Bacteriophage SPP1

Endolysin

Siphoviridae

Abstract

Background: To obtain Endolysin with impact(s) on gram-negative bacteria as well as gram-positive bacteria, N-acetylmuramyl L-alanine-amidase (MurNAc-LAA) from a Bacillus subtilis-hosted Siphoviridae phage (SPP1 phage, Subtilis Phage Pavia 1) was exogenously expressed in Escherichia coli (E. coli). Methods: The sequences of MurNAc-LAA genes encoding peptidoglycan hydrolases were obtained from the Virus-Host database. The sequence of MurNAc-LAA was optimized by GenScript software to generate MurNAc-LAA-MMI (LysM2) for optimal expression in E. coli. Furthermore, the structure and function of LysM2 was evaluated in silico. The optimized gene was synthesized, subcloned in the pET28a, and expressed in E. coli BL21(DE3). The antibacterial effects of the protein on the peptidoglycan substrates were studied. Results: LysM2, on 816 bp gene encoding a 33 kDa protein was confirmed as specific SPP1 phage enzyme. The enzyme is composed of 271 amino acids, with a half-life of 10 hr in E. coli. In silico analyses showed 34. 2% alpha-helix in the secondary structure, hydrophobic N-terminal, and lysine-rich C-terminal, and no antigenic properties in LysM2 protein. This optimized Endolysin revealed impacts against Proteus (sp) by turbidity, and an Antibacterial activity against Klebsiella pneumoniae, Salmonella typhimurium, and Proteus vulgaris in agar diffusion assays. Conclusion: Taken together, our results confirmed that LysM2 is an inhibiting agent for gram-negative bacteria.

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APA: Copy

MIRI, MORTEZA, Yazdianpour, Sepideh, ABOLMAALI, SHAMSOZOHA, & DARVISH ALIPOUR ASTANEH, SHAKIBA. (2022). Exogenous Production of N-acetylmuramyl-L Alanine Amidase (LysM2) from Siphoviridae Phage Affecting Anti-Gram-Negative Bacteria: Evaluation of Its Structure and Function. AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB), 14(1), 46-53. SID. https://sid.ir/paper/972081/en

Vancouver: Copy

MIRI MORTEZA, Yazdianpour Sepideh, ABOLMAALI SHAMSOZOHA, DARVISH ALIPOUR ASTANEH SHAKIBA. Exogenous Production of N-acetylmuramyl-L Alanine Amidase (LysM2) from Siphoviridae Phage Affecting Anti-Gram-Negative Bacteria: Evaluation of Its Structure and Function. AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB)[Internet]. 2022;14(1):46-53. Available from: https://sid.ir/paper/972081/en

IEEE: Copy

MORTEZA MIRI, Sepideh Yazdianpour, SHAMSOZOHA ABOLMAALI, and SHAKIBA DARVISH ALIPOUR ASTANEH, “Exogenous Production of N-acetylmuramyl-L Alanine Amidase (LysM2) from Siphoviridae Phage Affecting Anti-Gram-Negative Bacteria: Evaluation of Its Structure and Function,” AVICENNA JOURNAL OF MEDICAL BIOTECHNOLOGY (AJMB), vol. 14, no. 1, pp. 46–53, 2022, [Online]. Available: https://sid.ir/paper/972081/en

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