Source:http://linkedlifedata.com/resource/pubmed/id/16347392
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
7
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| pubmed:dateCreated |
2010-6-25
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| pubmed:abstractText |
A new Clostridium strain was isolated on starch at 60 degrees C. Starch, pullulan, maltotriose, and maltose induced the synthesis of alpha-amylase and pullulanase, while glucose, ribose, fructose, and lactose did not. The formation of the amylolytic enzymes was dependent on growth and occurred predominantly in the exponential phase. The enzymes were largely cell bound during growth of the organism with 0.5% starch, but an increase of the starch concentration in the growth medium was accompanied by the excretion of alpha-amylase and pullulanase into the culture broth; but also by a decrease of total activity. alpha-Amylase, pullulanase, and alpha-glucosidase were active in a broad temperature range (40 to 85 degrees C) and displayed temperature optima for activity at 60 to 70 degrees C. During incubation with starch under aerobic conditions at 75 degrees C for 2 h, the activity of both enzymes decreased to only 90 or 80%. The apparent K(m) values of alpha-amylase, pullulanase, and alpha-glucosidase for their corresponding substrates, starch, pullulan, and maltose were 0.35 mg/ml, 0.63 mg/ml, and 25 mM, respectively.
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| pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-16346789,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-16346790,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-16346791,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-238632,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-308745,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-3885852,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-390902,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-3934138,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-4705426,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-5340651,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-5684197,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-5690538,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-5874549,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-5938919,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-6154683,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16347392-6160813
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:month |
Jul
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| pubmed:issn |
0099-2240
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:volume |
53
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
1661-7
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| pubmed:dateRevised |
2010-9-20
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| pubmed:year |
1987
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| pubmed:articleTitle |
Thermostable amylolytic enzymes from a new clostridium isolate.
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| pubmed:affiliation |
Institut für Mikrobiologie der Georg-August Universität Göttingen, 3400 Göttingen, Federal Republic of Germany, and Department of Food Science and Technology, School of Agriculture, Nagoya University, Chikusa, Nagoya 464 Japan.
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| pubmed:publicationType |
Journal Article
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