Yayınlanmış 1 Ocak 2009
| Sürüm v1
Dergi makalesi
Açık
Cloning of a xylanase gene xyn2A from rumen fungus Neocallimastix sp GMLF2 in Escherichia coli and its partial characterization
- 1. Kahramanmaras Sutcu Imam Univ, Fac Agr, Dept Anim Sci, Biotechnol & Gene Engn Lab, Bahcelievler 46100, Kahramanmaras, Turkey
Açıklama
Anaerobic fungi belonging to the family Neocallimastigaceae are native inhabitants in the rumen of the most herbivores, such as cattle, sheep and goats. A member of this unique group, Neocallimastix sp. GMLF2 was isolated from cattle feces and screened for its xylanase encoding gene using polymerase chain reaction. The gene coding for a xylanase (xyn2A) was cloned in Escherichia coli and expression was monitored. To determine the enzyme activity, assays were conducted for both fungal xylanase and cloned xylanase (Xyl2A) for supernatant and cell-associated activities. Optimum pH and temperature of the enzyme were found to be 6.5 and 50A degrees C, respectively. The enzyme was stable at 40A degrees C and 50A degrees C for 20 min but lost most of its activity when temperature reached 60A degrees C for 5-min incubation time. Rumen fungal xylanase was mainly released to the supernatant of culture, while cloned xylanase activity was found as cell-associated. Multiple alignment of the amino acid sequences of Xyl2A with published xylanases from various organisms suggested that Xyl2A belongs to glycoside hydrolase family 11.
Dosyalar
bib-cfa2d3de-4e37-4bfb-8bfb-d11dff2c7c7a.txt
Dosyalar
(224 Bytes)
| Ad | Boyut | Hepisini indir |
|---|---|---|
|
md5:912a302eb7775c17eb47338745e20b66
|
224 Bytes | Ön İzleme İndir |