PURIFIKASI DAN KARAKTERISASI MANANASE DARI Saccharopolyspora flava 76
Mannan is one of major component of hemicelluloses that consist of mannose, galactose, and glucose with β-1,4 linkage. Mannanase catalyzes hydrolysis of mannan to mannose and manooligosaccharides. These mannose and manooligosaccharides have potential as functional food. Saccharopolyspora flava 76 i...
محفوظ في:
المؤلفون الرئيسيون: | , |
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التنسيق: | Theses and Dissertations NonPeerReviewed |
منشور في: |
[Yogyakarta] : Universitas Gadjah Mada
2012
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الموضوعات: | |
الوصول للمادة أونلاين: | https://repository.ugm.ac.id/97265/ http://etd.ugm.ac.id/index.php?mod=penelitian_detail&sub=PenelitianDetail&act=view&typ=html&buku_id=54302 |
الوسوم: |
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الملخص: | Mannan is one of major component of hemicelluloses that consist of
mannose, galactose, and glucose with β-1,4 linkage. Mannanase catalyzes
hydrolysis of mannan to mannose and manooligosaccharides. These mannose and
manooligosaccharides have potential as functional food. Saccharopolyspora flava
76 is belong to Biotechnology Culture Collection (BTCC)-LIPI, have ability to
produce mannanase. This research aims at finding purification steps for that
enzyme, characterize and analyse the hydrolysis of porang flour to
oligosaccharides by the mannanase. There are some steps in this research: (i)
qualitative and quantitative analyze of mannanase produced by S. flava 76, (ii)
production optimation, (iii) production and extraction of the enzyme, (iv)
purification,(v) characterization, and (vi) analysis of the ability of mannanase
enzymes hydrolyze porang flour into oligosaccharides. The isolate has an
mannanolitic index 4,63 and the highest enzyme activity of 2,47 U/ml on the
fourth days at 0,3% LBG substrate with addition 0,1% of mannose. The
purification consist of three step, concentration with poly etilene glycol 6000
(PEG 6000), ammonium sulfate precipitation, and gel filtration chromatography
with Sephadex G-75. Using PEG 6000 the enzyme activity rose to 3,59 times and
rose again 3,84 times after precipitated by 60% ammonium sulfate. This purified
enzyme was identified as β-mannanase based on its characteristics that was
optimum pH in neutral (7,0) phosphate buffer, optimum temperature at 50 °C,
molecular weight in 50 kDa and 60 kDa by SDS-PAGE, the kinetic of this
enzyme was Km = 0,505 mg/ml and Vmax = 0,732 µmol/hour, and its ability to
hydrolyzed porang flour (glucomannan) to abundant mannooligosaccharides such
as mannotriose, mannoheptose and monosaccharides such us mannose and
glucose in small quantities product. |
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