Protein engineering of invertase for enhancing yeast dough fermentation under high-sucrose conditions

. 2023 Apr ; 68 (2) : 207-217. [epub] 20221006

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid36201138

Grantová podpora
32100156 National Natural Science Foundation of China
21908004 National Natural Science Foundation of China
buctrc201801 Fundamental Research Funds for the Central Universities

Odkazy

PubMed 36201138
DOI 10.1007/s12223-022-01006-y
PII: 10.1007/s12223-022-01006-y
Knihovny.cz E-zdroje

During yeast dough fermentation, such as the high-sucrose bread-making process, the yeast cells are subjected to considerable osmotic stress, resulting in poor outcomes. Invertase is important for catalyzing the irreversible hydrolysis of sucrose to free glucose and fructose, and decreasing the catalytic activity of the invertase may reduce the glucose osmotic stress on the yeast. In this study, we performed structural design and site-directed mutagenesis (SDM) on the Saccharomyces cerevisiae invertase (ScInV) in an Escherichia coli expression system to study the catalytic activity of ScInV mutants in vitro. In addition, we generated the same mutation sites in the yeast endogenous genome and tested their invertase activity in yeast and dough fermentation ability. Our results indicated that appropriately reduced invertase activity of yeast ScInV can enhance dough fermentation activity under high-sucrose conditions by 52%. Our systems have greatly accelerated the engineering of yeast endogenous enzymes both in vitro and in yeast, and shed light on future metabolic engineering of yeast.

Zobrazit více v PubMed

Álvaro-Benito M, Polo A, González B et al (2010) Structural and kinetic analysis of Schwanniomyces occidentalis invertase reveals a new oligomerization pattern and the role of its supplementary domain in substrate binding. J Biol Chem 285:13930–13941 PubMed DOI PMC

An Y, Ji J, Wu W et al (2005) A rapid and efficient method for multiple-site mutagenesis with a modified overlap extension PCR. Appl Microbiol Biot 68:774–778 DOI

Badotti F, Dário MG, Alves SL et al (2008) Switching the mode of sucrose utilization by Saccharomyces cerevisiae. Microb Cell Fact 7:1–11 DOI

Batista FR, Hernández L, Fernández JR et al (1999) Substitution of Asp-309 by Asn in the Arg-Asp-Pro (RDP) motif of Acetobacter diazotrophicus levansucrase affects sucrose hydrolysis, but not enzyme specificity. Biochem J 337:503–506 PubMed DOI PMC

Fernandez-Moya R, Da Silva NA (2017) Engineering Saccharomyces cerevisiae for high-level synthesis of fatty acids and derived products. FEMS Yeast Res 17:fox071 DOI

Gomar-Alba M, Morcillo-Parra MÁ, del Olmo M, lí, (2015) Response of yeast cells to high glucose involves molecular and physiological differences when compared to other osmostress conditions. FEMS Yeast Res 15:1–14 DOI

Gong G, Zhang Y, Wang Z et al (2021) GTR 2.0: gRNA-tRNA array and Cas9-NG based genome disruption and single-nucleotide conversion in Saccharomyces cerevisiae. ACS Synth Biol 10:1328–1337 PubMed DOI

Hejlesen R, Füchtbauer EM (2020) Multiple site-directed mutagenesis via simple cloning by prolonged overlap extension. Biotechniques 68:345–348 PubMed DOI

Hernandez-Lopez MJ, Prieto JA, Randez-Gil F (2003) Osmotolerance and leavening ability in sweet and frozen sweet dough. Comparative analysis between Torulaspora delbrueckii and Saccharomyces cerevisiae baker’s yeast strains. Antonie Van Leeuwenhoek J G 84:125–134 DOI

Lagunas R (1993) Sugar transport in Saccharomyces cerevisiae. FEMS Microbiol Lett 10:229–242 DOI

Liang X, Peng L, Li K et al (2012) A method for multi-site-directed mutagenesis based on homologous recombination. Anal Biochem 427:99–101 PubMed DOI

Lin X, Zhang CY, Bai XW, Xiao DG (2015) Enhanced leavening ability of baker’s yeast by overexpression of SNR84 with PGM2 deletion. J Ind Microbiol Biot 42:939–948 DOI

Lin X, Zhang CY, Meng L et al (2018) Overexpression of SNF4 and deletions of REG1- and REG2-enhanced maltose metabolism and leavening ability of baker’s yeast in lean dough. J Ind Microbiol Biot 45:827–838 DOI

Nagy ZB, Felföldi F, Tamás L, Puskás LG (2004) A one-tube, two-step polymerase chain reaction-based site-directed mutagenesis method with simple identification of the mutated product. Anal Biochem 324:301–303 PubMed DOI

Nielsen J, Larsson C, van Maris A, Pronk J (2013) Metabolic engineering of yeast for production of fuels and chemicals. Curr Opin Biotech 24:398–404 PubMed DOI

Ozcan S, Johnston M (1999) Function and regulation of yeast hexose transporters. Microbiol Mol Biol R 63:554–569 DOI

Peng RH, Xiong AS, Yao QH (2006) A direct and efficient PAGE-mediated overlap extension PCR method for gene multiple-site mutagenesis. Appl Microbiol Biot 73:234–240 DOI

Rabhi I, Guedel N, Chouk I et al (2004) A novel simple and rapid PCR-based site-directed mutagenesis method. Mol Biotechnol 26:27–34 PubMed DOI

Sainz-Polo MA, Ramírez-Escudero M, Lafraya A et al (2013) Three-dimensional structure of Saccharomyces invertase: role of a non-catalytic domain in oligomerization and substrate specificity. J Biol Chem 288:9755–9766 PubMed DOI PMC

Sarokin L, Carlson M (1984) Upstream region required for regulated expression of the glucose-repressible SUC2 gene of Saccharomyces cerevisiae. Mol Cell Biol 4:2750–2757 PubMed PMC

Taussig R, Carlson M (1983) Nucleotide sequence of the yeast SUC2 gene for invertase. Nucleic Acids Res 11:1943–1954 PubMed DOI PMC

Tokashiki T, Yamamoto H, Watanabe H et al (2011) A functional compound contained in sugar cane molasses enhances the fermentation ability of baker’s yeast in high-sugar dough. J Gen Appl Microbiol 57:303–307 PubMed DOI

Tomás-Cobos L, Casadomé L, Mas G et al (2004) Expression of the HXT1 low affinity glucose transporter requires the coordinated activities of the HOG and glucose signalling pathways. J Biol Chem 279:22010–22019 PubMed DOI

Varga-Orvos Z, Nagy ZB, Mészáros A et al (2007) Multiplex site-directed mutagenesis strategy including high-efficiency selection of the mutant PCR products. Biotechnol Lett 29:1921–1925 PubMed DOI

Voordeckers K, Brown CA, Vanneste K et al (2012) Reconstruction of Ancestral Metabolic Enzymes Reveals Molecular Mechanisms Underlying Evolutionary Innovation through Gene Duplication. PLoS Biol 10:e1001446 PubMed DOI PMC

Zhang CY, Lin X, Feng B et al (2016) Enhanced leavening properties of baker’s yeast by reducing sucrase activity in sweet dough. Appl Microbiol Biot 100:6375–6383 DOI

Zhang Y, Nielsen J, Liu Z (2018) Metabolic engineering of Saccharomyces cerevisiae for production of fatty acid-derived hydrocarbons. Biotechnol Bioeng 115:2139–2147 PubMed DOI

Zhang Y, Wang J, Wang Z et al (2019) A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae. Nat Commun 10:1053 PubMed DOI PMC

Zhao Y (2021) Production of β-carotene in Saccharomyces cerevisiae through altering yeast lipid metabolism. Biotechnol Bioeng 118:2043–2052 PubMed DOI

Zimmermann FK, Khan NA, Eaton NR (1973) Identification of new genes involved in disaccharide fermentation in yeast. Mol Gen Genet 123:29–41 PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace