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2019
DOI: 10.1016/j.micres.2019.126342
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A script for initiating molecular biology studies with non-conventional yeasts based on Saccharomycopsis schoenii

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Cited by 9 publications
(11 citation statements)
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“…fibuligera . Thus, these fungi have a high potential for application in the fermentation industry, due to their strong amylolytic activity, secretion of amylases, acid protease, and β‐glucosidase (Kayacan et al, 2019). Bal et al (2014) identified S .…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…fibuligera . Thus, these fungi have a high potential for application in the fermentation industry, due to their strong amylolytic activity, secretion of amylases, acid protease, and β‐glucosidase (Kayacan et al, 2019). Bal et al (2014) identified S .…”
Section: Discussionmentioning
confidence: 99%
“…In Although we have detected Saccharomycopsis species associated with postharvest sour rot on fruit, the literature reports some species found in traditional fermented beverages, such as S. fibuligera. Thus, these fungi have a high potential for application in the fermentation industry, due to their strong amylolytic activity, secretion of amylases, acid protease, and β-glucosidase (Kayacan et al, 2019). Bal et al (2014) identified S. fibuligera in nuruk, the Korean starter culture used to make various types of Korean alcoholic beverages, including takju, cheongju, and soju.…”
Section: Pathogenicity Testmentioning
confidence: 99%
“…E1 is a diploid yeast strain. Thus, two rounds of PCR-based gene targeting were performed to delete both alleles of FOT1 and FOT2 using two dominant marker genes YES1 (provides G418-resistance) and YES3 (provides clonNAT-resistance) [ 60 ]. Generated mutants grew in the presence of both antibiotics, had correctly integrated both marker genes and had lost FOT1 and FOT2 ORFs ( Figure S2 ).…”
Section: Methodsmentioning
confidence: 99%
“…To test for promoter activity, the LacZ ORF was placed under the control of H. uvarum promoters using primers 7/8 (HuTEF1-promoter), 9/10 (HuFBA1-promoter), and 11/12 (HuPGK1-promoter), which added 40 bp of flanking homology region to pLacZ (Figure 1). The upstream region of the LacZ ORF [41] was removed by restriction digestion of pLacZ with KpnI and XhoI. The linearised vector and H. uvarum promoters (HuTEF1, HuFBA1, and HuPGK1) were transformed into yeast and fused to LacZ by in vivo recombination.…”
Section: Plasmid Design and Constructionmentioning
confidence: 99%