Short Communication
Characterization of Vesicle Differentiation Mutants of Frankia casuarinae
2020 年 35 巻 2 号 論文ID: ME19150
詳細
2020 年 35 巻 2 号 論文ID: ME19150
The nitrogen-fixing actinobacterium Frankia develops unique multicellular structures called vesicles, which are the site of nitrogen fixation. These vesicles are surrounded by a thick hopanoid lipid envelope that protects nitrogenase against oxygen inactivation. The phenotypes of five mutants that form smaller numbers of vesicles were investigated. The vesicles of these mutants were smaller than those of the wild type and had a phase dark appearance. They induced the expression of a glutamine synthetase gene in hyphae cells in response to ammonium starvation. These results suggest that genes impaired in the mutants do not function in global nitrogen regulation, but specifically function in vesicle differentiation.
Nitrogen is an essential element for all living organisms. Most organisms cannot utilize dinitrogen gas (N2) because of its stable triple bound. Nitrogen-fixing (N2-fixing) bacteria have the ability to reduce N2 to ammonia (NH3), and assimilate it to organic compounds such as amino acids. Fixed nitrogen flows into ecology, and, thus, N₂-fixing bacteria play an important role in global nitrogen cycles.
N2 fixation is catalyzed by nitrogenase, which is a complex metalloenzyme composed of dinitrogenase (NifDK) and dinitrogenase reductase (NifH) (Dixon and Kahn, 2004). Since nitrogenase is highly oxygen-labile, N2-fixing bacteria adopt diverse strategies (behavioral, physiological, and structural) to protect nitrogenase against oxygen inactivation (Gallon, 1992).
Frankia spp. are N2-fixing multicellular actinobacteria. Under NH3-depleted and aerobic conditions, Frankia develop spherical multicellular structures called vesicles (Fig. S1), which are the site for N2 fixation (Huss-danell, 1997). These vesicles are surrounded by a thick envelope composed of dozens of hopanoid lipid layers (Berry et al., 1993). Since the envelope functions as a barrier to oxygen penetration, nitrogenase, which is expressed inside vesicles, retains its activity (Benson and Silvester, 1993). Vesicles are not formed under anaerobic conditions and N2 fixation occurs in hyphal cells (Murry et al., 1985). Genes related to vesicle differentiation have not yet been identified, except for those related to hopanoid lipid synthesis, which are ubiquitous in the microbial world (Kannenberg and Poralla, 1999).
We previously isolated five N2-fixation mutants of Frankia casuarinae (G21E10, G23C4, G23D3, N7C9, and N10E6), which had smaller numbers of vesicles (<ca. 15% of the wild type) (Kucho et al., 2017) (Table S1). These mutants are considered to have defects in the generation of vesicle primordia. In the present study, we characterized the phenotypes of these mutants in more detail.
We used F. casuarinae strain CcI3 as the wild type (WT) (Nouioui et al., 2016). Frankia strains were grown in NH3-repleted (N+) BAP-TN+ liquid medium (Kucho et al., 2009) at 28°C with stirring until the mid-logarithmic phase, and cells were then transferred to NH3-depleted (N–) BAP-TN– medium (Kucho et al., 2009). Vesicles were observed 7 d after being transferred to N– conditions using phase-contrast (for size measurements) and dark-field (for envelope evaluations) optical systems with the microscope MT5310L (Meiji Techno). The vesicle sizes of G21E10, G23D3, N7C9, and N10E6 were markedly smaller than those of WT (<60%), while those of G23C4 were slightly smaller (80% of WT) (Fig. 1 and Table S1). When observed under the dark-field microscope, the thickness of the envelope was proportional to its brightness (Parsons et al., 1987) because the light effect was attributed to birefringence produced by structural layering of the vesicle envelope. In WT, approximately 40% of vesicles showed a bright appearance, indicative of a well-developed envelope (Fig. 2 asterisk and Fig. S2). Approximately 60% of WT vesicles also had a thick-walled stalk (Fig. 2 arrowhead and Fig. S2). In all mutants, the frequency of vesicles with a well-developed envelope was significantly less than that in WT and was markedly lower in G23C4 (5%) and N10E6 (0%) (Fig. 2 and S2). Furthermore, G23D3 and N10E6 produced fewer vesicles with a thick-walled stalk (Fig. 2 and S2). These results indicate that genes impaired in these mutants are important not only for the generation of primordia, but also for the maturation of vesicles (size expansion and envelope development).
Size of vesicles. Each dot represents an average calculated from between 20 and 36 independent vesicles from a biological replicate. The bar represents the standard error. Medians calculated from two biological replicates are shown by open boxes.
Dark-field microscopic images of vesicles. A vesicle and stalk with a well-developed envelope are shown by an asterisk and arrowhead, respectively. The bar represents 3 μm.
The genes impaired in these mutants may be directly involved in the vesicle differentiation process. Alternatively, these genes may function in the perception or signaling of a NH3-starvation status and their mutations indirectly disabled downstream vesicle differentiation (Fig. 3). To clarify the site of function, we investigated the expression of a NH3-responsive gene in hyphal cells. If the latter is the case, these mutants will not be able to induce gene expression in hyphal cells or induce vesicle formation (Fig. 3). Therefore, we focused on a glutamine synthetase (GS) gene, which converts NH3 and glutamate to glutamine. Frankia has two types of GS enzyme—GSI and GSII—that show distinct biochemical and regulatory properties, and the expression of the GSII gene was previously shown to be up-regulated in hyphal cells (and in vesicles) in response to NH3-starvation (Schultz and Benson, 1990; Ghodhbane-Gtari et al., 2014). We also investigated the expression of a gene involved in NH3-responsive regulation (ntrB, see below).
Schematic diagram of sequential events predicted to occur in Frankia in response to NH3 starvation under aerobic conditions. This is a working hypothesis that requires further evidence.
Frankia cells were acclimated to N– conditions as described above. Cells were collected by centrifugation 4 d after being transferred to N– conditions, and total RNA was purified by the cetyltrimethylammonium bromide (CTAB) method (Kucho et al., 2009). Contaminating DNA was removed by the TURBO DNA-free kit (Thermo Fisher Scientific). The cDNAs of the GSII (francci3_3143), ntrB (francci3_3178), and 16S rRNA (francci3_R0040, internal standard) genes were synthesized using PrimeScript reverse transcriptase (Takara Bio) in a 20-μL reaction mixture containing 1.5 μg of total RNA and 2 pmol of gene-specific reverse primers (GSII, Ghodhbane-Gtari et al., 2014; 16S rRNA, Kucho et al., 2017; ntrB, 5′-cccacatctcgggcagtt-3′) at 42°C for 30 min and then at 50°C for 15 min. Regarding GSII and 16S rRNA, real-time PCR was performed using the Probe qPCR mix (Takara Bio) in a 20-μL reaction mixture containing 4 pmol of forward and reverse primers (GSII, Ghodhbane-Gtari et al., 2014; 16S rRNA, Kucho et al., 2017), 4 pmol of the TaqMan probe (GSII, 5′-acgccatcgtcgcctgct-3′; 16S rRNA, Kucho et al., 2017), and cDNA derived from 100 ng (GSII) or 1 ng (16S rRNA) of total RNA. Regarding ntrB and 16S rRNA, semi-quantitative PCR was performed using EX Taq DNA polymerase (Takara Bio) in a 20-μL reaction mixture containing 4 pmol of a forward primer (ntrB, 5′-gccgctgaccagtgtgaa-3′; 16S rRNA, Kucho et al., 2017) and reverse primer (same primers used in reverse transcription), and cDNA derived from 100 ng (ntrB) or 1 ng (16S rRNA) of total RNA. A temperature regime (95°C for 30 s, 58°C for 30 s, and 72°C for 18 s) was repeated 28 times for ntrB or 23 times for 16S rRNA.
In WT, the mRNA levels of the GSII gene were markedly higher under N– than N+ conditions (Fig. 4). Under N– conditions, all mutant strains (G21E10, G23C4, G23D3, N7C9, and N10E6) showed similar GSII expression levels to WT and these levels appeared to be higher than those of N+ WT (Fig. 4 and Table S1). These results indicate that the mutants retained the abilities to perceive NH₃ starvation and transduce the signal to the GSII gene in hyphal cells in order to activate its expression. In many eubacteria, NH3-responsive regulation is accomplished by the nitrogen regulation (ntr) system (Merrick and Edwards, 1995), and homologs of its components (glnBD and ntrBC) have been found in Frankia genomes. Semi-quantitative reverse transcription PCR showed that an ntrB homolog (francci3_3178) was expressed in WT and all the mutant strains (Fig. 5 and Table S1). Genome analyses revealed that three of the mutants (G23C4, N7C9, and N10E6) did not carry mutations in these homologs (Kucho et al., 2017). Collectively, these results indicate that the genes responsible for the phenotypes of the three mutants are not related to global nitrogen regulation, but specifically function in the vesicle differentiation process (Fig. 3). The mutants G21E10 (Kucho et al., 2017) and G23D3 (K. Kucho, unpublished) carried an identical amino acid substitution in the homolog of ntrB (francci3_3178), whereas the same mutation was found in a revertant strain that formed vesicles and fixed N2 (K. Kucho, unpublished). Therefore, the mutation in the ntrB homolog did not appear to cause the mutant phenotypes and G21E10 and G23D3 may be impaired in other genes that specifically function in the vesicle differentiation process.
Expression of the GSII gene. Relative transcript levels to a value obtained from a WT N+ sample are shown. Averages calculated from three biological replicates are shown. The bar represents the standard error. N+, NH3-repleted; N–, NH3-depleted conditions.
Semi-quantitative reverse transcription PCR of ntrB (francci3_3178) and 16S rRNA (16S) genes. The expected sizes of the amplified products are 299 bp (ntrB) and 120 bp (16S rRNA). N+, NH3-repleted; N–, NH3-depleted conditions. Signals were weak when RNA samples without reverse transcription were used as templates (data not shown).
Vesicle differentiation-specific genes are considered to be unique for Frankia and have not yet been identified. Two laboratories recently reported the successful transformation of Frankia spp. (Gifford et al., 2019; Pesce et al., 2019). Using these methods, we will be able to identify the genes responsible for the mutant phenotypes using complementation experiments with a genomic library of the WT strain.
We thank Ms. Yasuka Nishimura for the analysis of vesicle sizes. This work was supported by MEXT KAKENHI 19K05772 and by a grant from the Institute for Fermentation, Osaka (IFO).
