Global changes in protein composition of N2-fixing-Azoarcus sp. strain BH72 upon diazosome formation
Open Access
- 1 October 1996
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 178 (19) , 5748-5754
- https://doi.org/10.1128/jb.178.19.5748-5754.1996
Abstract
The strictly respiratory, diazotrophic bacterium Azoarcus sp. strain BH72 fixes nitrogen under microaerobic conditions. In empirically optimized batch cultures at nanomolar O2 concentrations in the presence of proline, cells can shift into a state of higher activity and respiratory efficiency of N2 fixation in which intracytoplasmic membrane stacks (diazosomes) related to N2 fixation are formed. Induction of intracytoplasmic membranes is most pronounced in coculture of Azoarcus sp. strain BH72 with an ascomycete originating from the same host plant, Kallar grass. To initiate studies on function of diazosomes and regulation of their formation, diazosome-containing bacteria were compared with respect to composition or total cellular and membrane proteins with diazosome-free cells fixing nitrogen under standard conditions. In two-dimensional protein gels, we detected striking differences in protein patterns upon diazosome formation: (i) 7.3% of major proteins disappeared, and only 73% of the total proteins of control cells were detectable, indicating that diazosome-containing cells have a more specialized metabolism; (ii) nine new proteins appeared and five proteins increased in concentration, designated DP1 to DP 15; and (iii) five new major membrane proteins (MP1 to MP6) were detected, indicating that membranes might have specialized functions. N-terminal amino acid sequence analysis of DP1 to DP4 allowed us to preliminarily identify DP4 as the glnB gene product P(II), an intracellular signal transmitter known to be involved in the regulation of nitrogen metabolism. According to its electrophoretic mobility, it might be uridylylated in diazosome-free cells but not in diazosome-containing cells, or it may represent a second, not identical P(II) protein. Oligonucleotides deduced from N-terminal sequences of DP1 and DP4 specifically hybridized to chromosomal DNA of Azoarcus sp. strain BH72 in Southern hybridizations.This publication has 42 references indexed in Scilit:
- Induction of complex intracytoplasmic membranes related to nitrogen fixation in Azoarcus sp. BH72Molecular Microbiology, 1995
- An additional PIIinEscherichia coli: a new regulatory protein in the glutamine synthetase cascadeFEMS Microbiology Letters, 1995
- An additional PII in Escherichia coli: a new regulatory protein in the glutamine synthetase cascadeFEMS Microbiology Letters, 1995
- Effect of growth temperatures on the protein levels in a psychrotrophic bacterium, Pseudomonas fragiJournal of Bacteriology, 1994
- Uridylylation of the PII protein in Rhizobium leguminosarumFEBS Letters, 1993
- Azoarcus gen. nov., Nitrogen-Fixing Proteobacteria Associated with Roots of Kallar Grass (Leptochloa fusca (L.) Kunth), and Description of Two Species, Azoarcus indigens sp. nov. and Azoarcus communis sp. nov.International Journal of Systematic and Evolutionary Microbiology, 1993
- Stress proteins and cross-protection by heat shock and salt stress in Bacillus subtilisJournal of General Microbiology, 1992
- The gene‐protein database of Escherichia coli: Edition 4Electrophoresis, 1991
- Solubilization of Plant Membrane Proteins for Analysis by Two-Dimensional Gel ElectrophoresisPlant Physiology, 1986
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970