Archives of Microbiology

, Volume 171, Issue 4, pp 279–289

GroEL chaperonins are required for the formation of a functional nitrogenase in Bradyrhizobium japonicum

  • H.-M. Fischer
  • Karin Schneider
  • Markus Babst
  • Hauke Hennecke
Original paper

DOI: 10.1007/s002030050711

Cite this article as:
Fischer, HM., Schneider, K., Babst, M. et al. Arch Microbiol (1999) 171: 279. doi:10.1007/s002030050711

Abstract

At least five highly conserved, but disparately regulated groESL operons are present in Bradyrhizobium japonicum. Expression of groESL3 is coregulated with symbiotic nitrogen fixation genes, implying a role of GroESL chaperonins in the nitrogen fixation process. Null mutants of individual groEL genes, however, were not impaired in symbiotic nitrogen fixation activity. By contrast, the groEL3-plus-groEL4 double mutant strain D4, which is mutated in those groEL genes that contribute most to the GroEL pool under symbiotic conditions, exhibited less than 5% Fix activity as compared to the wild-type. Expression of lacZ fusions made to several representative nif and fix genes was not, or only marginally, reduced in mutant D4, indicating that the requirement of chaperonins for nitrogen fixation does not occur at the level of RegSR-NifA-σ54- or FixLJ-FixK2-dependent gene regulation. Instead, immunoblot analyses revealed that the level of NifH and NifDK nitrogenase proteins was drastically decreased in extracts prepared from D4 bacteroids and from free-living cells grown anaerobically. Transcriptional fusions of the anaerobically induced groESL3 promoter (P3) to all five B. japonicum groESL operons and also to groESL from Escherichia coli were integrated into the chromosome of mutant D4. Strains harboring P3 fused to groESL1, groESL2, groESL5, or E. coli groESL partially complemented the symbiotic defect of mutant D4, whereas the wild-type phenotype was completely restored in strains complemented with P3 fused to groESL3 (control) or groESL4. Likewise, the growth defect of an E. coli groEL mutant could be corrected at least partially by individual B. japonicum groESL operons. In conclusion, both series of complementation analyses were not indicative of a strict substrate specificity of any of the B. japonicum groESL gene products, which is in good agreement with their high degree of sequence conservation.

Key words Cpn60groESLHeat shock proteinHsp60NifANitrogen fixationSymbiosis

Copyright information

© Springer-Verlag Berlin Heidelberg 1999

Authors and Affiliations

  • H.-M. Fischer
    • 1
  • Karin Schneider
    • 1
  • Markus Babst
    • 1
  • Hauke Hennecke
    • 1
  1. 1.Mikrobiologisches Institut, Eidgenössische Technische Hochschule, Schmelzbergstrasse 7, CH-8092 Zürich, Switzerland e-mail: hfischer@micro.biol.ethz.ch Tel. +41-1-632-4419; Fax +41-1-632-1148CH