» Articles » PMID: 37347159

Dissecting the Arginine and Lysine Biosynthetic Pathways and Their Relationship in Haloarchaeon Natrinema Gari J7-2 Via Endogenous CRISPR-Cas System-Based Genome Editing

Overview
Specialty Microbiology
Date 2023 Jun 22
PMID 37347159
Authors
Affiliations
Soon will be listed here.
Abstract

The evolutionary relationship between arginine and lysine biosynthetic pathways has been well established in bacteria and hyperthermophilic archaea but remains largely unknown in haloarchaea. Here, the endogenous CRISPR-Cas system was harnessed to edit arginine and lysine biosynthesis-related genes in the haloarchaeon Natrinema gari J7-2. The Δ, Δ, Δ, and Δ mutant strains display an arginine auxotrophic phenotype, while the Δ mutant shows a lysine auxotrophic phenotype, suggesting that strain J7-2 utilizes the ArgW-mediated pathway and the diaminopimelate (DAP) pathway to synthesize arginine and lysine, respectively. Unlike the ArgD in Escherichia coli acting as a bifunctional aminotransferase in both the arginine biosynthesis pathway and the DAP pathway, the ArgD in strain J7-2 participates only in arginine biosynthesis. Meanwhile, in strain J7-2, the function of cannot be compensated for by its evolutionary counterpart in the DAP pathway. Moreover, strain J7-2 cannot utilize α-aminoadipate (AAA) to synthesize lysine via the ArgW-mediated pathway, in contrast to hyperthermophilic archaea that employ a bifunctional LysW-mediated pathway to synthesize arginine (or ornithine) and lysine from glutamate and AAA, respectively. Additionally, the replacement of a 5-amino-acid signature motif responsible for substrate specificity of strain J7-2 ArgX with that of its hyperthermophilic archaeal homologs cannot endow the Δ mutant with the ability to biosynthesize lysine from AAA. The analysis shows that strain J7-2 ArgX acts on glutamate rather than AAA. These results suggest that the arginine and lysine biosynthetic pathways of strain J7-2 are highly specialized during evolution. Due to their roles in amino acid metabolism and close evolutionary relationship, arginine and lysine biosynthetic pathways represent interesting models for probing functional specialization of metabolic routes. The current knowledge with respect to arginine and lysine biosynthesis is limited for haloarchaea compared to that for bacteria and hyperthermophilic archaea. Our results demonstrate that the haloarchaeon Natrinema gari J7-2 employs the ArgW-mediated pathway and the DAP pathway for arginine and lysine biosynthesis, respectively, and the two pathways are functionally independent of each other; meanwhile, ArgX is a key determinant of substrate specificity of the ArgW-mediated pathway in strain J7-2. This study provides new clues about haloarchaeal amino acid metabolism and confirms the convenience and efficiency of endogenous CRISPR-Cas system-based genome editing in haloarchaea.

Citing Articles

FBXW7 metabolic reprogramming inhibits the development of colon cancer by down-regulating the activity of arginine/mToR pathways.

Li Q, Li Y, Zhou T, Zhang Y, Li H, Yuan F PLoS One. 2025; 20(1):e0317294.

PMID: 39823500 PMC: 11741656. DOI: 10.1371/journal.pone.0317294.


HtrAs are essential for the survival of the haloarchaeon J7-2 in response to heat, high salinity, and toxic substances.

Luo H, Qu X, Deng X, He L, Wu Y, Liu Y Appl Environ Microbiol. 2024; 90(2):e0204823.

PMID: 38289131 PMC: 10880668. DOI: 10.1128/aem.02048-23.

References
1.
Ouchi T, Tomita T, Horie A, Yoshida A, Takahashi K, Nishida H . Lysine and arginine biosyntheses mediated by a common carrier protein in Sulfolobus. Nat Chem Biol. 2013; 9(4):277-83. DOI: 10.1038/nchembio.1200. View

2.
Pettersen E, Goddard T, Huang C, Couch G, Greenblatt D, Meng E . UCSF Chimera--a visualization system for exploratory research and analysis. J Comput Chem. 2004; 25(13):1605-12. DOI: 10.1002/jcc.20084. View

3.
Xu Y, Labedan B, Glansdorff N . Surprising arginine biosynthesis: a reappraisal of the enzymology and evolution of the pathway in microorganisms. Microbiol Mol Biol Rev. 2007; 71(1):36-47. PMC: 1847373. DOI: 10.1128/MMBR.00032-06. View

4.
Wang Y, Sima L, Lv J, Huang S, Liu Y, Wang J . Identification, Characterization, and Application of the Replicon Region of the Halophilic Temperate Sphaerolipovirus SNJ1. J Bacteriol. 2016; 198(14):1952-1964. PMC: 4936101. DOI: 10.1128/JB.00131-16. View

5.
Quintela J, Pittenauer E, Allmaier G, Aran V, de Pedro M . Structure of peptidoglycan from Thermus thermophilus HB8. J Bacteriol. 1995; 177(17):4947-62. PMC: 177270. DOI: 10.1128/jb.177.17.4947-4962.1995. View