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Rhizopus oligosporus and yeast co-cultivation during barley tempeh fermentation-Nutritional impact and real-time PCR quantification of fungal growth dynamics

Feng, X. M. (författare)
Department of Microbiology, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden,Sveriges lantbruksuniversitet (SLU),Swedish University of Agricultural Sciences (SLU)
Passoth, V. (författare)
Department of Microbiology, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden,Sveriges lantbruksuniversitet (SLU),Swedish University of Agricultural Sciences (SLU)
Eklund-Jonsson, Charlotte (författare)
Department of Chemical and Biological Engineering, Food Science, Chalmers University of Technology, Göteborg, Sweden,Chalmers tekniska högskola,Chalmers University of Technology
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Alminger, Marie, 1957 (författare)
Department of Chemical and Biological Engineering, Food Science, Chalmers University of Technology, Göteborg, Sweden,Chalmers tekniska högskola,Chalmers University of Technology
Schnürer, Johan, 1957- (författare)
Department of Microbiology, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden,Sveriges lantbruksuniversitet (SLU),Swedish University of Agricultural Sciences (SLU)
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 (creator_code:org_t)
London, United Kingdom : Elsevier BV, 2007
2007
Engelska.
Ingår i: Food microbiology (Print). - London, United Kingdom : Elsevier BV. - 0740-0020 .- 1095-9998. ; 24:4, s. 393-402
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Barley tempeh was produced by fermenting barley kernels with Rhizopus oligosporus. The potential of the yeasts Saccharomyces cerevisiae (three strains), S. boulardii (one strain), Pichia anomala (one strain) and Kluyveromyces lactis (one strain) to grow together with R. oligosporus during barley tempeh fermentation was evaluated. All yeast strains grew during the fermentation and even during cold storage of tempeh (P < 0.01). The growth of yeasts slightly increased the ergosterol contents, but did not influence amino acid contents and compositions, and did not reduce phytate contents. Slight increases of vitamins B6 and niacinamide, and slight decreases of B1 and biotin were observed. Quantification of fungal growth is difficult during mixed species fermentations because ergosterol is found in all fungal species, and colony-forming-unit (cfu) estimations are not reliable for R. oligosporus and other sporulating fungi. Therefore, we developed a quantitative real-time PCR method for individually quantifying S. cerevisiae and R. oligosporus growth in barley tempeh. The PCR results were highly correlated with the ergosterol content of R. oligosporus and with the number of cfu of S. cerevisiae. Thus, real-time PCR is a rapid and selective method to quantify yeasts and R. oligosporus during mixed species fermentation of inhomogenous substrate such as barley tempeh. © 2006 Elsevier Ltd. All rights reserved.

Ämnesord

NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Industriell bioteknik -- Annan industriell bioteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Industrial Biotechnology -- Other Industrial Biotechnology (hsv//eng)

Nyckelord

Barley tempeh
Nutrition
Real-time PCR
Rhizopus oligosporus
Yeast
article
barley
coculture
fermentation
food control
food handling
fungus spore
growth
development and aging
microbiology
polymerase chain reaction
Rhizopus
species difference
Coculture Techniques
Food Microbiology
Food Technology
Hordeum
Species Specificity
Spores
Fungal
Yeasts
Fungi
Hordeum vulgare subsp. vulgare
Kluyveromyces
Kluyveromyces lactis
Oligosporus
Pichia
Pichia anomala
Rhizopus microsporus var. oligosporus
Saccharomyces cerevisiae

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