Bernd Masepohl

Identification of a new class of nitrogen fixation genes in Rhodobacter capsalatus: a putative membrane complex involved in electron transport to nitrogenase

DNA sequence analysis of a 12236 by fragment, which is located upstream of nifE in Rhodobacter capsulatus nif region A, revealed the presence of ten open reading frames. With the exception of fdxC and fdxN, which encode a plant-type and a bacterial-type ferredoxin, the deduced products of these coding regions exhibited no significant homology to known proteins. Analysis of defined insertion and deletion mutants demonstrated that six of these genes were required for nitrogen fixation. Therefore, we propose to call these genes rnfA, rnfB, rnfC, rnfD, rnfE and rnfF (for Rhodobacter nitrogen fixation). Secondary structure predictions suggested that the rnf genes encode four potential membrane proteins and two putative iron-sulphur proteins, which contain cysteine motifs (C-X2-C-X2-C-X3-C-P) typical for [4Fe-4S] proteins. Comparison of the in vivo and in vitro nitrogenase activities of fdxN and rnf mutants suggested that the products encoded by these genes are involved in electron transport to nitrogenase. In addition, these mutants were shown to contain significantly reduced amounts of nitrogenase. The hypothesis that this new class of nitrogen fixation genes encodes components of an electron transfer system to nitrogenase was corroborated by analysing the effect of metronidazole. Both the fdxN and rnf mutants had higher growth yields in the presence of metronidazole than the wild type, suggesting that these mutants contained lower amounts of reduced ferredoxins.

Genetic characterization and sequence analysis of the duplicated nifA/nifB gene region of Rhodobacter capsulatus

SummaryA DNA region showing homology to Klebsiella pneumoniae nifA and nifB is duplicated in Rhodobacter capsulatus. The two copies of this region are called nifA/nifB copy I and nifA/nifB copy II. Deletion mutagenesis demonstrated that either of the two copies is sufficient for growth in nitrogen-free medium. In contrast, a double deletion mutant turned out to be deficient in nitrogen fixation. The complete nucleotide sequence of a 4838 bp fragment containing nifA/nifB copy I was determined. Two open reading frames coding for a 59653 (NifA) and a 49453 (NifB) dalton protein could be detected. Comparison of the amino acid sequences revealed that the R. capsulatus nifA and nifB gene products are more closely related to the NifA and NifB proteins of Rhizobium meliloti and Rhizobium leguminosarum than to those of K. pneumoniae. A rho-independent termination signal and a typical nif promoter region containing a putative NifA binding site and a consensus nif promoter are located within the region between the R. capsulatus nifA and nifB genes. The nifB sequence is followed by an open reading frame (ORF1) coding for a 27721 dalton protein in nifA/nifB copy I. DNA sequence analysis of nifA/nifB copy II showed that both copies differ in the DNA region downstream of nifB and in the noncoding sequence in front of nifA. All other regions compared, i.e. the 5′ part of nifA, the intergenic region and the 3′ part of nifB, are identical in both copies.

nif gene expression studies in Rhodobacter capsulatus: nfrC‐independent repression by high ammonium concentrations

The expression of nif genes in Rhodobacter capsulatus depends on the two regulatory genes, rpoN and nifA, encoding a nif‐specific alternative sigma factor of RNA polymerase and a nif‐specific transcriptional activator, respectively. The expression of the rpoN gene itself is also RPON/NIFA dependent. In order to better characterize the regulation of nif gene induction, chromosomal nifH‐, rpoN‐, nifAl‐ and nifA2‐ lacZ fusions were constructed and the expression of these different nif‐lacZ fusions was determined under photoheterotrophic conditions at different starting ammonium concentrations. The two nifA genes were found to be induced first, followed by nifH and finally by rpoN upon weak, medium and strong nitrogen starvation, respectively. This induction profile and the correlation between the expression of the different nif genes suggested that nifAl expression is the limiting factor for nif gene induction. This hypothesis was tested by construction of different nifA1 overexpressing mutants. Contrary to the current model of n/Y gene expression in R. capsulatus, which predicted constitutive nif gene expression in such mutants, a strong repression of nifH and rpoW was found at high ammonium concentration. The low nifH expression under these conditions is unaffected by nifA2 and is not increased in a ntrC mutant, ruling out any role of NTRC as a mediator of this repression. This finding implies an additional, so far unidentified, regulation by fixed nitrogen in R capsulatus. Changing the expression level of rpoN indicated that low levels of RPON are already sufficient for full nifH induction. The nifA1 and rpoN expression mutants were also tested for diazotrophic growth. Similar generation times were determined for the mutants and for the wild type, but diazotrophic growth of the nifA1 overexpressing ntrC mutant RCM14 did not start until after a prolonged lag phase of two to three days.

Organization and regulation of genes encoding the molybdenum nitrogenase and the alternative nitrogenase in Rhodobacter capsulatus

Abstract The phototrophic non-sulfur purple bacterium Rhodobacter capsulatus is able to fix atmospheric dinitrogen either via a conventional molybdenum nitrogenase or via an alternative iron-only nitrogenase. At least 53 genes are involved in the synthesis and regulation of these two nitrogenase systems, most of which are clustered in four regions widely spread in the genome. Expression of both nitrogenase systems is regulated at the transcriptional level by NifR1 and NifR2, homologues of NtrC and NtrB, respectively. However, this ntr system is only involved in the regulation of the two nitrogenase systems and the high-affinity molybdenum transport system and is not required for utilization of other N sources such as proline and arginine. In contrast to enteric bacteria, the R. capsulatus NtrC homologue does not act in concert with the alternative sigma factor RpoN (σ54). Nitrogen fixation in R. capsulatus is regulated at the transcriptional level and also at the post-translational level. The draTG gene products are responsible for covalent modification of the dinitrogenase reductases of both nitrogenase systems. In addition, mutations in hvrA, a gene previously described as being responsible for low-light activation of the photosynthetic apparatus, also affect regulation of nitrogen fixation.

Yeast two-hybrid studies on interaction of proteins involved in regulation of nitrogen fixation in the phototrophic bacterium Rhodobacter capsulatus.

Rhodobacter capsulatus contains two PII-like proteins, GlnB and GlnK, which play central roles in controlling the synthesis and activity of nitrogenase in response to ammonium availability. Here we used the yeast two-hybrid system to probe interactions between these PII-like proteins and proteins known to be involved in regulating nitrogen fixation. Analysis of defined protein pairs demonstrated the following interactions: GlnB-NtrB, GlnB-NifA1, GlnB-NifA2, GlnB-DraT, GlnK-NifA1, GlnK-NifA2, and GlnK-DraT. These results corroborate earlier genetic data and in addition show that PII-dependent ammonium regulation of nitrogen fixation in R. capsulatus does not require additional proteins, like NifL in Klebsiella pneumoniae. In addition, we found interactions for the protein pairs GlnB-GlnB, GlnB-GlnK, NifA1-NifA1, NifA2-NifA2, and NifA1-NifA2, suggesting that fine tuning of the nitrogen fixation process in R. capsulatus may involve the formation of GlnB-GlnK heterotrimers as well as NifA1-NifA2 heterodimers. In order to identify new proteins that interact with GlnB and GlnK, we constructed an R. capsulatus genomic library for use in yeast two-hybrid studies. Screening of this library identified the ATP-dependent helicase PcrA as a new putative protein that interacts with GlnB and the Ras-like protein Era as a new protein that interacts with GlnK.

Genetics and regulation of nitrogen fixation in free-living bacteria.

Series Preface. Preface. List of Contributors. Dedication. 1: Historical Perspective - Development of nif Genetics and Regulation in Klebsiella pneumoniae R. Dixon 1. Introduction 2. The Early Years 3. Defining the K. pneumoniae nif Genes 4. The Recombinant DNA Era 5. nif Gene Regulation 6. Coda References 2: Genetics of Nitrogen Fixation and Related Aspects of Metabolism in Species of Azotobacter: History and Current Status C. Kennedy and P. Bishop 1. Research on the Genus Azotobacter (1901-2003) 2. Application of the Tools of Genetics and Molecular Biology in Species of Azotobacter 3. The nif Genes encoding the Enzymes for Structure, Function, and Biosynthesis of Mo-containing Nitrogenase 4. Regulation of Expression of nif and Associated Genes by Ammonium and O2 5. Ancillary Properties of Azotobacter Species that Aid the Efficiency of Nitrogen Fixation 6. Discovery of Molybdenum-independent Nitrogenase Systems in A. vinelandii 7. Molybdenum-independent Nitrogenase systems in other Azotobacter Species Acknowledgements References 3: Nitrogen Fixation in the Clostridia J.-S. Chen 1. Introduction 2. The Nitrogen-fixing Clostridia 3. Distinctive Features of the nif Genes of the Clostridia 4. Genes of Ammonia Assimilation 5. Regulation of Nitrogen Fixation and Ammonia Assimilation 6. Concluding Remarks References 4: Regulation of Nitrogen Fixation in Methanogenic Archaea J.A. Leigh 1. Introduction 2. History and Background 3. Transcriptional Regulation 4. Regulation of Nitrogenase Activity 5. Summary References 5: Nitrogen Fixation in Heterocyst-Forming Cyanobacteria T. Thiel 1.Introduction 2. Structure of Heterocysts 3. Nitrogenase Genes 4. Heterocyst Metabolism 5. Genes Important for Heterocyst Formation 6. heterocyst Pattern Formation 7. Regulation Acknowledgements References 6: N2 Fixation by Non-Heterocystous Cyanobacteria J.R. Gallon 1. Introduction 2. Non-heterocystous Cyanobacteria 3. Patterns of N2 Fixation Acknowledgements References 7: Nitrogen Fixation in the Photosynthetic Purple Bacterium Rhodobacter capsulatus B. Masepohl, T. Drepper and W. Klipp 1. Introduction 2. Organization of Nitrogen-fixing Genes 3. The Nitrogen-fixation Regulon of R. capsulatus 4. Ammonium Control of Synthesis and Activity of both Nitrogenases 5. Environmental Factors Controlling Nitrogen Fixation 6. Linkage of Nitrogen Fixation, Photosynthesis, and Carbon Dioxide Assimilation 7. Nitrogen Fixation in other Photosynthetic Purple Bacteria References 8: Post-translational Regulation of Nitorgenase in Photosynthetic Bacteria S. Nordlund and P.W. Ludden 1. Introduction 2. Discovery of Nitrogen Fixation by Photosynthetic Bacteria 3. In vitro Studies of Nitrogenase in Photosynthetic Bacteria 4. The Protein Era 5. Evidence for the Drat/Drag System in other Organisms 6. Other ADP-Ribosylations 7. Genetics of the Drag/Drat System 8. Signal Transduction to Drat and Drat 9. Conclustions Acknowledgement References 9: Regulation of Nitrogen Fixation in Free-Living Diazotrophs M.J. Merrick 1. Introduction 2. General Nitrogen Control Systems 3. nif-specific Nitrogen Control 4. Nitrogen Control of Nitrogenase Activity 5. Conclusions References 10: Molybdenum Uptake and Homeostatis R.N. Pau 1. Molybdenum Outside Cells 2.

DNA sequence and genetic analysis of the Rhodobacter capsulatus nifENX gene region: Homology between NifX and NifB suggests involvement of NifX in processing of the iron-molybdenum cofactor

SummaryRhodobacter capsulatus genes homologous to Klebsiella pneumoniae nifE, nifN and nifX were identified by DNA sequence analysis of a 4282 bp fragment of nif region A. Four open reading frames coding for a 51188 (NifE), a 49459 (NifN), a 17459 (NifX) and a 17472 (ORF4) dalton protein were detected. A typical NifA activated consensus promoter and two imperfect putative NifA binding sites were located in the 377 bp sequence in front of the nifE coding region. Comparison of the deduced amino acid sequences of R. capsulatus NifE and NifN revealed homologies not only to analogous gene products of other organisms but also to the α and β subunits of the nitrogenase iron-molybdenum protein. In addition, the R. capsulatus nifE and nifN proteins shared considerable homology with each other. The map position of nifX downstream of nifEN corresponded in R. capsulatus and K. pneumoniae and the deduced molecular weights of both proteins were nearly identical. Nevertheless, R. capsulatus NifX was more related to the C-terminal end of NifY from K. pneumoniae than to NifX. A small domain of approximately 33 amino acid residues showing the highest degree of homology between NifY and NifX was also present in all nifB proteins analyzed so far. This homology indicated an evolutionary relationship of nifX, nifY and nifB and also suggested that NifX and NifY might play a role in maturation and/or stability of the iron-molybdenum cofactor. The open reading rame (ORF4) downstream of nifX in R. capsulatus is also present in Azotobacter vinelandii but not in K. pneumoniae. Interposon-induced insertion and deletion mutants proved that nifE and nifN were necessary for nitrogen fixation in R. capsulatus. In contrast, no essential role could be demonstrated for nifX and ORF4 whereas at least one gene downstream of ORF4 appeared to be important for nitrogen fixation.

The cyanobacterium Synechococcus sp. strain PCC 7942 contains a second alkaline phosphatase encoded by phoV.

A gene (phoV) encoding an alkaline phosphatase from Synechococcus sp. strain PCC 7942 was isolated by screening a plasmid gene bank for expression of alkaline phosphatase activity in Escherichia coli JM103. Two independent clones carrying the same alkaline-phosphatase-encoding gene were isolated. One of these clones (pKW1) was further analysed and the nucleotide sequence of a contiguous 3234 bp DNA fragment was determined. Two complete open reading frames (ORF1 and phoV) and an incomplete ORF3 were identified reading in the same direction. The deduced phoV gene product showed 34% identity to the alkaline phosphatase PhoA from Zymomonas mobilis, and the N-terminal part of the putative ORF3 protein exhibited 57% identity to a protein of unknown function from Frankia sp. Insertional inactivation of the Synechococcus PCC 7942 phoV gene failed, indicating an essential role for either the phoV or the ORF3 gene product. PhoV consists of 550 amino acid residues, resulting in a molecular mass of 61.3 kDa. To overexpress the Synechococcus PCC 7942 phoV gene in E. coli, plasmid pKW1 was transformed into a phoA mutant of E. coli (CC118). In E. coli strain CC118(pKW1) PhoV was expressed constitutively with high rates of activity, and was shown to be membrane associated in the periplasmic space. After partial purification of the recombinant PhoV, it was shown that, like other alkaline phosphatases, the Synechococcus PhoV had a broad pH optimum in the alkaline region and a broad substrate specificity for phosphomonoesters, required Zn2+ for activity, and was inhibited by phosphate. In contrast to several other alkaline phosphatases, PhoV was inhibited by Mn2+. Due to the lack of a Synechococcus PCC 7942 phoV mutant strain, the function of PhoV remains uncertain. However, the present results show that Synechococcus PCC 7942 has a second, probably phosphate-irrepressible, alkaline phosphatase (PhoV, 61.3 kDa) in addition to the phosphate-repressible enzyme (PhoA, 145 kDa) already described.

Nucleotide sequence and genetic analysis of the Rhodobacter capsulatus ORF6-nifU I SVW gene region: possible role of Nif W in homocitrate processing

DNA sequence analysis of a 3494-bp HindIII-Bc1I fragment of the Rhodobacter capsulatus nif region A revealed genes that are homologous to ORF6, nifU, nifS, nifV and nifW from Azotobacter vinelandii and Klebsiella pneumoniae. R. capsulatus nifU, which is present in two copies, encodes a novel type of NifU protein. The deduced amino acid sequences of NifUI and NifUII share homology only with the C-terminal domain of NifU from A. vinelandii and K. pneurnoniae. In contrast to nifA andnifB which are almost perfectly duplicated, the predicted amino acid sequences of the two NifU proteins showed only 39% sequence identity. Expression of the ORF6-nifUISVW operon, which is preceded by a putative σ54-dependent promoter, required the function of NifA and the nif-specific rpoN gene product encoded by nifR4. Analysis of defined insertion and deletion mutants demonstrated that only nifS was absolutely essential for nitrogen fixation in R. capsulatus. Strains carrying mutations in nifV were capable of very slow diazotrophic growth, whereas ORF6, nifUI and nifW mutants as well as a nifUI/nifUII, double mutant exhibited a Nif+ phenotype. Interestingly, R. capsulatus nifV mutants were able to reduce acetylene not only to ethylene but also to ethane under conditions preventing the expression of the alternative nitrogenase system. Homocitrate added to the growth medium repressed ethane formation and cured the NifV phenotype in R. capsulatus. Higher concentrations of homocitrate were necessary to complement the NifV phenotype of a polar nifV mutant (NifV−NifW−), indicating a possible role of NifW either in homocitrate transport or in the incorporation of this compound into the iron-molybdenum cofactor of nitrogenase.

Nitrogen and Molybdenum Control of Nitrogen Fixation in the Phototrophic Bacterium Rhodobacter capsulatus

The vast majority of the purple nonsulfur photosynthetic bacteria are diazotrophs, but the details of the complex regulation of the nitrogen fixation process are well understood only for a few species. Here we review what is known of the well-studied Rhodobacter capsulatus, which contains two different nitrogenases, a standard Mo-nitrogenase and an alternative Fe-nitrogenase, and which has overlapping transcriptional control mechanisms with regard to the presence of fixed nitrogen, oxygen, and molybdenum as well as the capability for the post-translational control of both nitrogenases in response to ammonium. R. capsulatus has two PII proteins, GlnB and GlnK, which play key roles in nitrogenase regulation at each of three different levels: activation of transcription of the nif-specific activator NifA, the post-translational control of NifA activity, and the regulation of nitrogenase activity through either ADP-ribosylation of NifH or an ADP-ribosylation-independent pathway. We also review recent work that has led to a detailed characterization of the molybdenum transport and regulatory system in R. capsulatus that ensures activity of the Mo-nitrogenase and repression of the Fe-nitrogenase, down to extremely low levels of molybdenum.