SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY

An extracellular lipase (Lip)-encoding gene from Streptomyces albus G has been cloned and sequenced. It encodes a Lip with 82% sequence identity to another previously cloned Lip from a Streptomyces species not closely related. These two sequences can be aligned with 33% identity to the sequence of L...

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Format: Other Non-Article Part of Journal/Newspaper
Language:unknown
Published: ELSEVIER SCIENCE BV 1994
Subjects:
Online Access:http://wrap.warwick.ac.uk/20554/
id ftuwarwick:oai:wrap.warwick.ac.uk:20554
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spelling ftuwarwick:oai:wrap.warwick.ac.uk:20554 2023-05-15T13:37:24+02:00 SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY 1994-06-24 http://wrap.warwick.ac.uk/20554/ unknown ELSEVIER SCIENCE BV UNSPECIFIED (1994) SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY. GENE, 144 (1). pp. 141-142. QH426 Genetics Journal Item NonPeerReviewed 1994 ftuwarwick 2022-03-16T20:17:00Z An extracellular lipase (Lip)-encoding gene from Streptomyces albus G has been cloned and sequenced. It encodes a Lip with 82% sequence identity to another previously cloned Lip from a Streptomyces species not closely related. These two sequences can be aligned with 33% identity to the sequence of Lip1 from the antarctic psychrotroph Moraxella TA144 [G. Feller et al., Nucleic Acids Res. 18 (1990) 6431]. An alignment of the three sequences revealed amino-acid substitutions which might be responsible for the greater thermal stability of the Streptomyces lipases. The presence of this lip gene family in several members of the Streptomyces genus was also shown. Other Non-Article Part of Journal/Newspaper Antarc* Antarctic The University of Warwick: WRAP - Warwick Research Archive Portal Antarctic The Antarctic
institution Open Polar
collection The University of Warwick: WRAP - Warwick Research Archive Portal
op_collection_id ftuwarwick
language unknown
topic QH426 Genetics
spellingShingle QH426 Genetics
SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
topic_facet QH426 Genetics
description An extracellular lipase (Lip)-encoding gene from Streptomyces albus G has been cloned and sequenced. It encodes a Lip with 82% sequence identity to another previously cloned Lip from a Streptomyces species not closely related. These two sequences can be aligned with 33% identity to the sequence of Lip1 from the antarctic psychrotroph Moraxella TA144 [G. Feller et al., Nucleic Acids Res. 18 (1990) 6431]. An alignment of the three sequences revealed amino-acid substitutions which might be responsible for the greater thermal stability of the Streptomyces lipases. The presence of this lip gene family in several members of the Streptomyces genus was also shown.
format Other Non-Article Part of Journal/Newspaper
title SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
title_short SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
title_full SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
title_fullStr SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
title_full_unstemmed SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY
title_sort sequence of the streptomyces-albus-g lipase-encoding gene reveals the presence of a prokaryotic lipase family
publisher ELSEVIER SCIENCE BV
publishDate 1994
url http://wrap.warwick.ac.uk/20554/
geographic Antarctic
The Antarctic
geographic_facet Antarctic
The Antarctic
genre Antarc*
Antarctic
genre_facet Antarc*
Antarctic
op_relation UNSPECIFIED (1994) SEQUENCE OF THE STREPTOMYCES-ALBUS-G LIPASE-ENCODING GENE REVEALS THE PRESENCE OF A PROKARYOTIC LIPASE FAMILY. GENE, 144 (1). pp. 141-142.
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