Dergiler / Turkish Journal of Biology / 2010 / Cilt: 34 - Sayı: 2

The Effects of the Pho85 Signaling Pathway on the Invertase Biosynthesis and Glucose Uptake in Saccharomyces cerevisiae

Sayfa
103–108
Yayın Tarihi
2010-02-01
DOI
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Our results indicated that Pho85p functions are essential for the regulated biosynthesis of the invertase enzyme from the SUC2 gene and for the high levels of glucose uptake in S. cerevisiae.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Glucose signaling controls a wide range of metabolic events in the yeast Saccharomyces cerevisiae.
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Temel Bulgular & Veri:Pho85p is a cyclin-dependent protein kinase that controls different metabolic events upon binding to its cyclin partners in the cytoplasm of yeast cells.
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Sonuç & Katkı:Our results indicated that Pho85p functions are essential for the regulated biosynthesis of the invertase enzyme from the SUC2 gene and for the high levels of glucose uptake in S. cerevisiae.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Pho85 · glucose sensing · glucose uptake

Özet

Glucose signaling controls a wide range of metabolic events in the yeast Saccharomyces cerevisiae. Glucose sensing and signaling processes require a variety of membrane-bound and cytoplasmic sensor proteins. Pho85p is a cyclin-dependent protein kinase that controls different metabolic events upon binding to its cyclin partners in the cytoplasm of yeast cells. In this study, we investigated the roles of Pho85p in the glucose signaling pathways that control invertase biosynthesis and glucose uptake in yeast. The biosynthesis of invertase enzyme from the SUC2 gene is controlled by glucose repression and derepression mechanisms in S. cerevisiae. However, the results of this research indicated that invertase biosynthesis occurs at low levels in a deregulated manner in the Dpho85 mutant yeast strain. Furthermore, our results showed that the biosynthesis of invertase is not repressed when the Dpho85 mutant is exposed to high levels of glucose. Moreover, we found that the glucose consumption rate of the Dpho85 mutant is at least 2-fold lower than that of the wild-type yeast strain. Our results indicated that Pho85p functions are essential for the regulated biosynthesis of the invertase enzyme from the SUC2 gene and for the high levels of glucose uptake in S. cerevisiae.

Abstract

Glucose signaling controls a wide range of metabolic events in the yeast Saccharomyces cerevisiae. Glucose sensing and signaling processes require a variety of membrane-bound and cytoplasmic sensor proteins. Pho85p is a cyclin-dependent protein kinase that controls different metabolic events upon binding to its cyclin partners in the cytoplasm of yeast cells. In this study, we investigated the roles of Pho85p in the glucose signaling pathways that control invertase biosynthesis and glucose uptake in yeast. The biosynthesis of invertase enzyme from the SUC2 gene is controlled by glucose repression and derepression mechanisms in S. cerevisiae. However, the results of this research indicated that invertase biosynthesis occurs at low levels in a deregulated manner in the Dpho85 mutant yeast strain. Furthermore, our results showed that the biosynthesis of invertase is not repressed when the Dpho85 mutant is exposed to high levels of glucose. Moreover, we found that the glucose consumption rate of the Dpho85 mutant is at least 2-fold lower than that of the wild-type yeast strain. Our results indicated that Pho85p functions are essential for the regulated biosynthesis of the invertase enzyme from the SUC2 gene and for the high levels of glucose uptake in S. cerevisiae.

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Bu Makaleye Atıf Yap

TÜRKEL*, S., ARIK, E. (2010). The Effects of the Pho85 Signaling Pathway on the Invertase Biosynthesis and Glucose Uptake in Saccharomyces cerevisiae. Turkish Journal of Biology, Cilt: 34 - Sayı: 2, 103–108. https://ajindex.com/articles/182380

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Kaynakça (2)

  1. Carlson M. Regulation of glucose utilization in yeast. Curr Opin Genet Dev 8: 560-564, 1998.
  2. Rolland F, Winderickx J, Thevelein JM. Glucose-sensing and - signaling mechanisms in yeast. FEMS Yeast Res 2: 183-201,