WebApr 10, 2024 · B.licheniformis DW2:icd: Increased the flux through TCA cycle: ATP content increased by 73.7%; bacitracin titer increased by 11.5%: Liu et al., 2024: B.licheniformis DW2:zwf: Strengthening NADPH generation: NADPH content increased by 61.24%; bacitracin titer increased by 12.43%: Zhu et al., 2024: Transcription factor engineering; B ... WebJul 7, 2024 · AbrB is a negative transcriptional regulator of pulcherriminic acid biosynthesis. To gain insights into the relationship between AbrB and pulcherriminic acid biosynthesis, the abrB deletion strain DW2 ΔabrB was constructed from the wild-type strain B. licheniformis DW2. Like its abrB deletion and overexpression derivative strains, DW2 began …
Multilevel metabolic engineering of Bacillus licheniformis for de …
WebApr 25, 2024 · Strains, plasmids, and cultivation conditions. The strains and plasmids used in this study are provided in Table 1.The primers used for strain construction and RT-qPCR were listed in Table S1. B. licheniformis DW2 was served as the original strain for constructing recombinants.Escherichia coli DH5α acted as the host for plasmid … WebFeb 8, 2024 · In this report, the mechanisms of B. licheniformis DW2 resistance to 2-PE were studied by multi-omics technology coupled with physiological and molecular biological approaches. 2-PE induced ... glass cubes for walls
Microbial synthesis of bacitracin: Recent progress, challenges, and ...
WebSep 14, 2024 · Strains, plasmids, and cultivation conditions. The strains and plasmids used in this study were listed in Table 1. B. licheniformis DW2 was severed as the original strain for constructing recombinants, and E. coli DH5α was served as the host for plasmid construction. The plasmid pHY300PLK was applied for constructing gene overexpression … WebBacillus licheniformis is a bacterium commonly found in the soil. It is found on bird feathers, especially chest and back plumage, and most often in ground-dwelling birds (like … WebMay 17, 2024 · Recently, Li et al. integrated a CRISPR-Cas9 nickase into the genome of B. licheniformis DW2, which successfully preserved the size of the genome-editing vector to guarantee a certain transformation rate . Although overexpression of the integrated nickase gene driven by the strong constitutive promoter P43 ensured successful genome editing, … g2010 hcpcs code