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fluorescent s aureus atcc 49230 strain  (ATCC)


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    Structured Review

    ATCC fluorescent s aureus atcc 49230 strain
    Fluorescent S Aureus Atcc 49230 Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 900 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/strain+atcc/Staphylococcus+aureus+subsp%2E+aureus+Rosenbach/10__22203_slash_ecm__v033a11-80-21-24
    Average 99 stars, based on 900 article reviews
    fluorescent s aureus atcc 49230 strain - by Bioz Stars, 2026-09
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    other:

    Article Title: Microbiome markers and uses thereof
    Article Snippet: In certain aspects the bacterial strain of Megasphaera elsdenii is strain ATCC-25940.

    Article Title: Biological Characteristics and Comparative Genomic Analysis of Corynebacterium hindlerae from Bovine Skin Abscess
    Article Snippet: Among 8 species of 12 Corynebacterium strains, strain ATCC-13032 contained significantly higher numbers of multicopy homologous genes, specific paralogs, and unique gene families compared to other Corynebacterium species, indicating specific expansion of gene families in Corynebacterium glutamicum .

    Data-independent acquisition:

    Article Title: A two-step actin-mediated strategy enables Campylobacter jejuni to promote mitochondrial aggregation and iron homeostasis, for intracellular survival and persistence.
    Article Snippet: .. Resulting DIA raw files were searched against A. castellanii (strain ATCC 30010 / Neff) or C. jejuni subsp. jejuni O:2 (strain ATCC 700819 / NCTC 11168), following analysis pipeline within PEAKS Studio software (Bioinformatics Solutions Inc, version 12). ..

    Software:

    Article Title: A two-step actin-mediated strategy enables Campylobacter jejuni to promote mitochondrial aggregation and iron homeostasis, for intracellular survival and persistence.
    Article Snippet: .. Resulting DIA raw files were searched against A. castellanii (strain ATCC 30010 / Neff) or C. jejuni subsp. jejuni O:2 (strain ATCC 700819 / NCTC 11168), following analysis pipeline within PEAKS Studio software (Bioinformatics Solutions Inc, version 12). ..

    Activity Assay:

    Article Title: Comparative Genetic Analysis of Pectinase Genes PGU of the Yeast Saccharomyces cerevisiae: Selection of Strains with High Pectinolytic Activity
    Article Snippet: Large-scale screening of the pectinolytic activity of Saccharomyces cerevisiae strains isolated from different types of wines, grape berries, fermenting must, fruit and berry juices, natural sources, and industrial waste from different regions of the world was carried out.. Of the 305 strains studied, the majority (249) did not produce active endopolygalacturonase.. According to the results obtained, the ability to hydrolyze pectin is generally not characteristic of the species S. cerevisiae.

    Article Title: Beyond a single species: Mapping virulence traits across the redefined Fusobacterium nucleatum complex
    Article Snippet: .. However, in strain ATCC 25,586, this autocatalytic activity is less efficient, leading to a full-length, membrane-anchored protease. ..

    Membrane:

    Article Title: Beyond a single species: Mapping virulence traits across the redefined Fusobacterium nucleatum complex
    Article Snippet: .. However, in strain ATCC 25,586, this autocatalytic activity is less efficient, leading to a full-length, membrane-anchored protease. ..

    Transformation Assay:

    Article Title: Bioengineering of Probiotic Yeast Saccharomyces boulardii for Advanced Biotherapeutics.
    Article Snippet: Saccharomyces cerevisiae var. boulardii (Sb), a subspecies of S. cerevisiae (Sc), is widely recognized for its probiotic properties.. Recently, Sb has attracted growing interest as a chassis organism for engineered live biotherapeutics and advanced microbiome therapies.. Traditional genetic manipulation techniques developed for Sc are now being successfully adapted for Sb, facilitating diverse genome integration strategies to enable the in situ biomanufacturing of functional molecules for disease intervention.

    Concentration Assay:

    Article Title: Bioengineering of Probiotic Yeast Saccharomyces boulardii for Advanced Biotherapeutics.
    Article Snippet: Saccharomyces cerevisiae var. boulardii (Sb), a subspecies of S. cerevisiae (Sc), is widely recognized for its probiotic properties.. Recently, Sb has attracted growing interest as a chassis organism for engineered live biotherapeutics and advanced microbiome therapies.. Traditional genetic manipulation techniques developed for Sc are now being successfully adapted for Sb, facilitating diverse genome integration strategies to enable the in situ biomanufacturing of functional molecules for disease intervention.

    Polymerase Chain Reaction:

    Article Title: Bioengineering of Probiotic Yeast Saccharomyces boulardii for Advanced Biotherapeutics.
    Article Snippet: Saccharomyces cerevisiae var. boulardii (Sb), a subspecies of S. cerevisiae (Sc), is widely recognized for its probiotic properties.. Recently, Sb has attracted growing interest as a chassis organism for engineered live biotherapeutics and advanced microbiome therapies.. Traditional genetic manipulation techniques developed for Sc are now being successfully adapted for Sb, facilitating diverse genome integration strategies to enable the in situ biomanufacturing of functional molecules for disease intervention.

    Amplification:

    Article Title: Bioengineering of Probiotic Yeast Saccharomyces boulardii for Advanced Biotherapeutics.
    Article Snippet: Saccharomyces cerevisiae var. boulardii (Sb), a subspecies of S. cerevisiae (Sc), is widely recognized for its probiotic properties.. Recently, Sb has attracted growing interest as a chassis organism for engineered live biotherapeutics and advanced microbiome therapies.. Traditional genetic manipulation techniques developed for Sc are now being successfully adapted for Sb, facilitating diverse genome integration strategies to enable the in situ biomanufacturing of functional molecules for disease intervention.



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    ATCC c glutamicum fm 1 strain
    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    ATCC vrsa strains atcc 700699
    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    ATCC acinetobacter baumannii bouvet and grimont
    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    ATCC staphylococcus aureus subsp. aureus rosenbach
    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    ATCC streptococcus agalactiae strain atcc baa
    Improving the tolerance to formaldehyde via ALE. (A) Growth <t>of</t> <t>FM-1</t> in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).
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    Improving the tolerance to formaldehyde via ALE. (A) Growth of FM-1 in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Improving the tolerance to formaldehyde via ALE. (A) Growth of FM-1 in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).

    Article Snippet: To assess the toxicity of formaldehyde in C. glutamicum ATCC 13032 lacking the formaldehyde dissimilation pathway, we cultivated a previously developed C. glutamicum FM-1 strain ( C. glutamicum ATCC 13032 Δ adhE Δ ald ), which was referred to as MX-1 in our previous study [ ], in CGXII medium supplemented with various concentrations of formaldehyde ( A).

    Techniques: Mutagenesis

    Effects of single-site mutations on formaldehyde tolerance. (A) Frequency of mutations of four bases in evolved strain FM-3. (B) Growth of strain FM-1 and its derivatives harboring single-site mutations on CGXII minimal agar medium supplemented with 10 g/L glucose and 1 mM formaldehyde. (C) Growth curves of strain FM-1 and its derivatives in CGXII medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Statistical significance at 31 h between FM-1- cgl1199 1015−1032del and FM-1 was determined by unpaired two-tailed Student's t -test: ∗∗∗P < 0.001.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Effects of single-site mutations on formaldehyde tolerance. (A) Frequency of mutations of four bases in evolved strain FM-3. (B) Growth of strain FM-1 and its derivatives harboring single-site mutations on CGXII minimal agar medium supplemented with 10 g/L glucose and 1 mM formaldehyde. (C) Growth curves of strain FM-1 and its derivatives in CGXII medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Statistical significance at 31 h between FM-1- cgl1199 1015−1032del and FM-1 was determined by unpaired two-tailed Student's t -test: ∗∗∗P < 0.001.

    Article Snippet: To assess the toxicity of formaldehyde in C. glutamicum ATCC 13032 lacking the formaldehyde dissimilation pathway, we cultivated a previously developed C. glutamicum FM-1 strain ( C. glutamicum ATCC 13032 Δ adhE Δ ald ), which was referred to as MX-1 in our previous study [ ], in CGXII medium supplemented with various concentrations of formaldehyde ( A).

    Techniques: Two Tailed Test

    Transcriptome analysis of FM-3 and FM-1 cultivated with or without formaldehyde stress. (A) Volcano plots of differential transcription levels in 1F vs. 1N, 3F vs. 3N, 3N vs. 1N, and 3F vs. 1F. (B) Changes in mRNA levels of genes involved in central metabolism and the respiratory chain between FM-3 and FM-1. Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Upregulated and downregulated genes are indicated with red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Transcriptome analysis of FM-3 and FM-1 cultivated with or without formaldehyde stress. (A) Volcano plots of differential transcription levels in 1F vs. 1N, 3F vs. 3N, 3N vs. 1N, and 3F vs. 1F. (B) Changes in mRNA levels of genes involved in central metabolism and the respiratory chain between FM-3 and FM-1. Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Upregulated and downregulated genes are indicated with red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Article Snippet: To assess the toxicity of formaldehyde in C. glutamicum ATCC 13032 lacking the formaldehyde dissimilation pathway, we cultivated a previously developed C. glutamicum FM-1 strain ( C. glutamicum ATCC 13032 Δ adhE Δ ald ), which was referred to as MX-1 in our previous study [ ], in CGXII medium supplemented with various concentrations of formaldehyde ( A).

    Techniques:

    Comparison of proteomes between FM-3 and FM-1 cultivated with formaldehyde or without formaldehyde stress. Functional classification of transcriptome differences based on KEGG_small_class annotation in 3N vs. 1N (A), 3F vs. 1F (B). Proteins with differentially expression in 1F vs. 1N (C) and 3F vs. 3N (D). Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Proteins exhibiting increased or decreased abundance are highlighted in red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Comparison of proteomes between FM-3 and FM-1 cultivated with formaldehyde or without formaldehyde stress. Functional classification of transcriptome differences based on KEGG_small_class annotation in 3N vs. 1N (A), 3F vs. 1F (B). Proteins with differentially expression in 1F vs. 1N (C) and 3F vs. 3N (D). Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Proteins exhibiting increased or decreased abundance are highlighted in red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Article Snippet: To assess the toxicity of formaldehyde in C. glutamicum ATCC 13032 lacking the formaldehyde dissimilation pathway, we cultivated a previously developed C. glutamicum FM-1 strain ( C. glutamicum ATCC 13032 Δ adhE Δ ald ), which was referred to as MX-1 in our previous study [ ], in CGXII medium supplemented with various concentrations of formaldehyde ( A).

    Techniques: Comparison, Functional Assay, Expressing

    Effects of Cgl1590 mutations on formaldehyde tolerance. (A) Amino acid sequence alignment between Cgl1590 and its derivatives. (B) Effects of cgl1590 truncation on formaldehyde tolerance. (C) Effects of cgl1590 knock-out on formaldehyde tolerance. (D) Effects of cgl1590 overexpression on formaldehyde tolerance. Cells were treated with 0.8 mM formaldehyde as stress condition. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Analysis of cell length and morphology of FM-1 without formaldehyde stress (E), FM-1 containing cgl1590 750insG mutation without formaldehyde stress (F), FM-1 with formaldehyde stress (G), and FM-1 strain containing cgl1590 750insG mutation with formaldehyde stress (H). All strains were grown in CGXII minimal medium supplemented with 10 g/L glucose, with or without 0.8 mM formaldehyde, and examined by SEM. Cell length was determined by measuring 70 cells of each strain and analyzed using ImageJ software. Statistical significance at 36 h between FM-1-△ cgl1590 and FM-1 was determined by two-tailed Student's t -test: ∗∗∗P < 0.001.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Effects of Cgl1590 mutations on formaldehyde tolerance. (A) Amino acid sequence alignment between Cgl1590 and its derivatives. (B) Effects of cgl1590 truncation on formaldehyde tolerance. (C) Effects of cgl1590 knock-out on formaldehyde tolerance. (D) Effects of cgl1590 overexpression on formaldehyde tolerance. Cells were treated with 0.8 mM formaldehyde as stress condition. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Analysis of cell length and morphology of FM-1 without formaldehyde stress (E), FM-1 containing cgl1590 750insG mutation without formaldehyde stress (F), FM-1 with formaldehyde stress (G), and FM-1 strain containing cgl1590 750insG mutation with formaldehyde stress (H). All strains were grown in CGXII minimal medium supplemented with 10 g/L glucose, with or without 0.8 mM formaldehyde, and examined by SEM. Cell length was determined by measuring 70 cells of each strain and analyzed using ImageJ software. Statistical significance at 36 h between FM-1-△ cgl1590 and FM-1 was determined by two-tailed Student's t -test: ∗∗∗P < 0.001.

    Article Snippet: To assess the toxicity of formaldehyde in C. glutamicum ATCC 13032 lacking the formaldehyde dissimilation pathway, we cultivated a previously developed C. glutamicum FM-1 strain ( C. glutamicum ATCC 13032 Δ adhE Δ ald ), which was referred to as MX-1 in our previous study [ ], in CGXII medium supplemented with various concentrations of formaldehyde ( A).

    Techniques: Sequencing, Knock-Out, Over Expression, Mutagenesis, Software, Two Tailed Test

    Improving the tolerance to formaldehyde via ALE. (A) Growth of FM-1 in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Improving the tolerance to formaldehyde via ALE. (A) Growth of FM-1 in minimal medium with 10 g/L glucose and different formaldehyde concentrations. 0 mM (square), 0.5 mM (triangle), 0.8 mM (circle), and 1 mM (inverted triangle). (B) ALE procedure of culture-1 in CGXII minimal medium supplemented with different formaldehyde concentrations and 10 g/L glucose. (C) Growth curve of the evolved mutants in CGXII minimal medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. (D) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose and 1.6 mM formaldehyde. (E) Growth curve of evolved mutant in CGXII minimal medium supplemented with 10 g/L glucose. (F) Formaldehyde degradation during cell growth of wild-type C. glutamicum ATCC 13032, FM-1 and FM-3. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3).

    Article Snippet: Strain FM-1 ( C. glutamicum ATCC 13032 Δ adhE Δ ald ) and its derivatives were cultivated at 30 °C in TSB medium [ ] or CGXII minimal medium [ ] supplemented with 10 g/L glucose as the carbon source, and formaldehyde (0.8–2.6 mM) was added to provide a stress condition as required.

    Techniques: Mutagenesis

    Effects of single-site mutations on formaldehyde tolerance. (A) Frequency of mutations of four bases in evolved strain FM-3. (B) Growth of strain FM-1 and its derivatives harboring single-site mutations on CGXII minimal agar medium supplemented with 10 g/L glucose and 1 mM formaldehyde. (C) Growth curves of strain FM-1 and its derivatives in CGXII medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Statistical significance at 31 h between FM-1- cgl1199 1015−1032del and FM-1 was determined by unpaired two-tailed Student's t -test: ∗∗∗P < 0.001.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Effects of single-site mutations on formaldehyde tolerance. (A) Frequency of mutations of four bases in evolved strain FM-3. (B) Growth of strain FM-1 and its derivatives harboring single-site mutations on CGXII minimal agar medium supplemented with 10 g/L glucose and 1 mM formaldehyde. (C) Growth curves of strain FM-1 and its derivatives in CGXII medium supplemented with 10 g/L glucose and 0.8 mM formaldehyde. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Statistical significance at 31 h between FM-1- cgl1199 1015−1032del and FM-1 was determined by unpaired two-tailed Student's t -test: ∗∗∗P < 0.001.

    Article Snippet: Strain FM-1 ( C. glutamicum ATCC 13032 Δ adhE Δ ald ) and its derivatives were cultivated at 30 °C in TSB medium [ ] or CGXII minimal medium [ ] supplemented with 10 g/L glucose as the carbon source, and formaldehyde (0.8–2.6 mM) was added to provide a stress condition as required.

    Techniques: Two Tailed Test

    Transcriptome analysis of FM-3 and FM-1 cultivated with or without formaldehyde stress. (A) Volcano plots of differential transcription levels in 1F vs. 1N, 3F vs. 3N, 3N vs. 1N, and 3F vs. 1F. (B) Changes in mRNA levels of genes involved in central metabolism and the respiratory chain between FM-3 and FM-1. Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Upregulated and downregulated genes are indicated with red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Transcriptome analysis of FM-3 and FM-1 cultivated with or without formaldehyde stress. (A) Volcano plots of differential transcription levels in 1F vs. 1N, 3F vs. 3N, 3N vs. 1N, and 3F vs. 1F. (B) Changes in mRNA levels of genes involved in central metabolism and the respiratory chain between FM-3 and FM-1. Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Upregulated and downregulated genes are indicated with red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Article Snippet: Strain FM-1 ( C. glutamicum ATCC 13032 Δ adhE Δ ald ) and its derivatives were cultivated at 30 °C in TSB medium [ ] or CGXII minimal medium [ ] supplemented with 10 g/L glucose as the carbon source, and formaldehyde (0.8–2.6 mM) was added to provide a stress condition as required.

    Techniques:

    Comparison of proteomes between FM-3 and FM-1 cultivated with formaldehyde or without formaldehyde stress. Functional classification of transcriptome differences based on KEGG_small_class annotation in 3N vs. 1N (A), 3F vs. 1F (B). Proteins with differentially expression in 1F vs. 1N (C) and 3F vs. 3N (D). Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Proteins exhibiting increased or decreased abundance are highlighted in red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Comparison of proteomes between FM-3 and FM-1 cultivated with formaldehyde or without formaldehyde stress. Functional classification of transcriptome differences based on KEGG_small_class annotation in 3N vs. 1N (A), 3F vs. 1F (B). Proteins with differentially expression in 1F vs. 1N (C) and 3F vs. 3N (D). Only significant changes (log 2 (fold change) ≥1 or ≤ −1, FDR≤0.05) are shown. Proteins exhibiting increased or decreased abundance are highlighted in red and blue, respectively. 1F, FM-1 cultivated with formaldehyde stress. 1N, FM-1 cultivated without formaldehyde stress. 3F, FM-3 cultivated with formaldehyde stress. 3N, FM-3 cultivated without formaldehyde stress.

    Article Snippet: Strain FM-1 ( C. glutamicum ATCC 13032 Δ adhE Δ ald ) and its derivatives were cultivated at 30 °C in TSB medium [ ] or CGXII minimal medium [ ] supplemented with 10 g/L glucose as the carbon source, and formaldehyde (0.8–2.6 mM) was added to provide a stress condition as required.

    Techniques: Comparison, Functional Assay, Expressing

    Effects of Cgl1590 mutations on formaldehyde tolerance. (A) Amino acid sequence alignment between Cgl1590 and its derivatives. (B) Effects of cgl1590 truncation on formaldehyde tolerance. (C) Effects of cgl1590 knock-out on formaldehyde tolerance. (D) Effects of cgl1590 overexpression on formaldehyde tolerance. Cells were treated with 0.8 mM formaldehyde as stress condition. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Analysis of cell length and morphology of FM-1 without formaldehyde stress (E), FM-1 containing cgl1590 750insG mutation without formaldehyde stress (F), FM-1 with formaldehyde stress (G), and FM-1 strain containing cgl1590 750insG mutation with formaldehyde stress (H). All strains were grown in CGXII minimal medium supplemented with 10 g/L glucose, with or without 0.8 mM formaldehyde, and examined by SEM. Cell length was determined by measuring 70 cells of each strain and analyzed using ImageJ software. Statistical significance at 36 h between FM-1-△ cgl1590 and FM-1 was determined by two-tailed Student's t -test: ∗∗∗P < 0.001.

    Journal: Synthetic and Systems Biotechnology

    Article Title: Multi-omics analyses of evolved Corynebacterium glutamicum mutants reveal the molecular responses to formaldehyde stress

    doi: 10.1016/j.synbio.2026.01.020

    Figure Lengend Snippet: Effects of Cgl1590 mutations on formaldehyde tolerance. (A) Amino acid sequence alignment between Cgl1590 and its derivatives. (B) Effects of cgl1590 truncation on formaldehyde tolerance. (C) Effects of cgl1590 knock-out on formaldehyde tolerance. (D) Effects of cgl1590 overexpression on formaldehyde tolerance. Cells were treated with 0.8 mM formaldehyde as stress condition. Values and error bars reflect the mean ± s.d. of three biological replicates (N = 3). Analysis of cell length and morphology of FM-1 without formaldehyde stress (E), FM-1 containing cgl1590 750insG mutation without formaldehyde stress (F), FM-1 with formaldehyde stress (G), and FM-1 strain containing cgl1590 750insG mutation with formaldehyde stress (H). All strains were grown in CGXII minimal medium supplemented with 10 g/L glucose, with or without 0.8 mM formaldehyde, and examined by SEM. Cell length was determined by measuring 70 cells of each strain and analyzed using ImageJ software. Statistical significance at 36 h between FM-1-△ cgl1590 and FM-1 was determined by two-tailed Student's t -test: ∗∗∗P < 0.001.

    Article Snippet: Strain FM-1 ( C. glutamicum ATCC 13032 Δ adhE Δ ald ) and its derivatives were cultivated at 30 °C in TSB medium [ ] or CGXII minimal medium [ ] supplemented with 10 g/L glucose as the carbon source, and formaldehyde (0.8–2.6 mM) was added to provide a stress condition as required.

    Techniques: Sequencing, Knock-Out, Over Expression, Mutagenesis, Software, Two Tailed Test