Nitric Oxide and Oxygen Regulate Truncated Hemoglobin Gene Expression inFrankiaStrain CcI3
Author(s) -
James Niemann,
Louis S. Tisa
Publication year - 2008
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.01100-08
Subject(s) - frankia , biology , nitric oxide , snap , gene expression , oxygen , hemoglobin , gene , strain (injury) , biochemistry , microbiology and biotechnology , symbiosis , genetics , bacteria , chemistry , root nodule , computer graphics (images) , organic chemistry , anatomy , computer science , endocrinology
The Frankia genome contains two truncated hemoglobin genes (hboN and hboO) whose functions remain to be determined. Nitric oxide (NO) generated by the addition of 400 microM SNAP (S-nitroso-N-acetylpenicillamine) caused a 10-fold increase in hboN gene expression but had no effect on hboO expression. The addition of the NO scavenger, carboxy-PT10, reduced the effect of SNAP. hboO gene expression increased under low-oxygen conditions, while hboN expression was unaffected. These results suggest that HboN may function in protection from nitrosative stress and that HboO may act as an oxygen transport molecule for increased respiration in hypoxic environments.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom