Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1998-7-23
pubmed:abstractText
In the strictly aerobic, gram-negative bacterium Vitreoscilla strain C1, oxygen-limited growth conditions create a more than 50-fold increase in the expression of a homodimeric heme protein which was recognized as the first bacterial hemoglobin (Hb). The recently determined crystal structure of Vitreoscilla Hb has indicated that the heme pocket of microbial globins differs from that of eukaryotic Hbs. In an attempt to understand the diverse functions of Hb-like proteins in prokaryotes, we have cloned and characterized the gene (vgb) encoding an Hb-like protein from another strain of Vitreoscilla, V. stercoraria DW. Several silent changes were observed within the coding region of the V. stercoraria vgb gene. Apart from that, V. stercoraria Hb exhibited interesting differences between the A and E helices. Compared to its Hb counterpart from Vitreoscilla strain C1, the purified preparation of V. stercoraria Hb displays a slower autooxidation rate. The differences between Vitreoscilla Hb and V. stercoraria Hb were mapped onto the three-dimensional structure of Vitreoscilla Hb, which indicated that the four changes, namely, Ile7Val, Ile9Thr, Ile10Ser, and Leu62Val, present within the V. stercoraria Hb fall in the region where the A and E helices contact each other. Therefore, alteration in the relative orientation of the A and E helices and the corresponding conformational change in the heme binding pocket of V. stercoraria Hb can be correlated to its slower autooxidation rate. In sharp contrast to the oxygen-regulated biosynthesis of Hb in Vitreoscilla strain C1, production of Hb in V. stercoraria has been found to be low and independent of oxygen control, which is supported by the absence of a fumarate and nitrate reductase regulator box within the V. stercoraria vgb promoter region. Thus, the regulation mechanisms of the Hb-encoding gene appear to be quite different in the two closely related species of Vitreoscilla. The relatively slower autooxidation rate of V. stercoraria Hb, lack of oxygen sensitivity, and constitutive production of Hb suggest that it may have some other function(s) in the cellular physiology of V. stercoraria DW, together with facilitated oxygen transport, predicted for earlier reported Vitreoscilla Hb.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-1311160, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-1594608, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-1609281, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2025413, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2034230, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2198533, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2483729, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2681149, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2685332, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-2850971, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-3067078, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-3277067, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-3736670, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-388439, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-3949777, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-4369125, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-4369203, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-6260575, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-6501229, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-7896850, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8125952, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8306987, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8394684, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8650150, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8682784, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-8808940, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-9115439, http://linkedlifedata.com/resource/pubmed/commentcorrection/9603838-9439594
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0099-2240
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2220-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1998
pubmed:articleTitle
Hemoglobin biosynthesis in Vitreoscilla stercoraria DW: cloning, expression, and characterization of a new homolog of a bacterial globin gene.
pubmed:affiliation
Institute of Microbial Technology, Chandigarh-160014, India.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't