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s cerevisiae strain s288c  (ATCC)


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    Structured Review

    ATCC s cerevisiae strain s288c
    S Cerevisiae Strain S288c, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 520 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/s+cerevisiae+s288c/Saccharomyces+cerevisiae+Meyen+ex+E%2EC%2E+Hansen/pm41513117-40-0-4
    Average 96 stars, based on 520 article reviews
    s cerevisiae strain s288c - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Comparison:

    Article Title: Host analysis-guided selection and targeted engineering (HASTE) of Lipomyces tetrasporus for the conversion of CO 2 -derived feedstocks.
    Article Snippet: • Lipomyces tetrasporus converts lignocellulosic hydrolysates and electrocatalytic

    Clone Assay:

    Article Title: <i>Corynebacterium glutamicum</i> for Microbial Production of Chitin Oligosaccharides Using Modular Engineering
    Article Snippet: We prepared sensitized C. glutamicum ATCC 13032, ATCC 13869, and S9114 cells according to the standard method described for C. glutamicum competent corneal cells. .. We cloned the N‐acetylglucosamine transferase (NodC)‐ and glucose‐ 6‐phosphate acetyltransferase (Gna1)‐encoding genes from T. autumnalis and S. cerevisiae S288C, respectively, into the high‐copy vector pJYW‐4 and transformed them into C. glutamicum ATCC 13032, ATCC 13869, and S9114 competent cells. ..

    Plasmid Preparation:

    Article Title: <i>Corynebacterium glutamicum</i> for Microbial Production of Chitin Oligosaccharides Using Modular Engineering
    Article Snippet: We prepared sensitized C. glutamicum ATCC 13032, ATCC 13869, and S9114 cells according to the standard method described for C. glutamicum competent corneal cells. .. We cloned the N‐acetylglucosamine transferase (NodC)‐ and glucose‐ 6‐phosphate acetyltransferase (Gna1)‐encoding genes from T. autumnalis and S. cerevisiae S288C, respectively, into the high‐copy vector pJYW‐4 and transformed them into C. glutamicum ATCC 13032, ATCC 13869, and S9114 competent cells. ..

    Transformation Assay:

    Article Title: <i>Corynebacterium glutamicum</i> for Microbial Production of Chitin Oligosaccharides Using Modular Engineering
    Article Snippet: We prepared sensitized C. glutamicum ATCC 13032, ATCC 13869, and S9114 cells according to the standard method described for C. glutamicum competent corneal cells. .. We cloned the N‐acetylglucosamine transferase (NodC)‐ and glucose‐ 6‐phosphate acetyltransferase (Gna1)‐encoding genes from T. autumnalis and S. cerevisiae S288C, respectively, into the high‐copy vector pJYW‐4 and transformed them into C. glutamicum ATCC 13032, ATCC 13869, and S9114 competent cells. ..

    other:

    Article Title: Hexadecanoic acid produced in the co-culture of S. cerevisiae and E.coli promotes oxidative stress tolerance of the S.cerevisiae cells.
    Article Snippet: Co-fermentation performed by Saccharomyces cerevisiae and Escherichia coli or other microbes has been widely used in industrial fermentation.. Meanwhile, the co-cultured microbes might regulate each other’s metabolisms or cell behaviors including oxidative stress tolerance through secreting molecules.. Here, results based on the co-culture system of S. cerevisiae and E. coli suggested the promoting effect of E. coli on the oxidative stress tolerance of S. cerevisiae cells.

    Article Title: Hexadecanoic acid enhances the oxidative tolerance of Saccharomyces cerevisiae via regulating MF(α)2 to mitigate cell cycle progression
    Article Snippet: Our previous research suggested that the co-cultivation of Escherichia coli and Saccharomyces cerevisiae could enhance the oxidative tolerance of yeast, and identified hexadecanoic acid as a key metabolic regulator.. Nevertheless, the precise regulatory mechanisms remain unclear.. The objective of this work is to elucidate the mechanism through which hexadecanoic acid enhances the oxidative tolerance of S. cerevisiae.

    Article Title: Promotion effect suggested by hexadecanoic acid on the oxidative tolerance of S. cerevisiae during its co-culture with E. coli
    Article Snippet: Materials and Methods Strains, media and culture conditions Both S. cerevisiae S288c (ATCC 204508) and E. coli (DE3) were purchased from the Institute of Microbiology, Chinese Academy of Sciences (IMCAS).

    Sequencing:

    Article Title: Increasing export of 2'fucosyllactose from microbial cells through the expression of a heterologous nucleic acid
    Article Snippet: One clone was designated HS0012. pTRP1-KO-URA3 A pBlueScript plasmid previously modified to contain the URA3 gene from S. cerevisiae was further modified to contain DNA sequences targeting URA3 to the TRP1 locus. .. Genomic DNA prepared from S. cerevisiae S288c, (sequence available from NCBI referencing ATCC 204508) was used as template for three PCR reactions as follows. ..

    Polymerase Chain Reaction:

    Article Title: Increasing export of 2'fucosyllactose from microbial cells through the expression of a heterologous nucleic acid
    Article Snippet: One clone was designated HS0012. pTRP1-KO-URA3 A pBlueScript plasmid previously modified to contain the URA3 gene from S. cerevisiae was further modified to contain DNA sequences targeting URA3 to the TRP1 locus. .. Genomic DNA prepared from S. cerevisiae S288c, (sequence available from NCBI referencing ATCC 204508) was used as template for three PCR reactions as follows. ..



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