Abstract

Sinorhizobium meliloti forms a symbiosis with the legume alfalfa, whereby it differentiates into a nitrogen-fixing bacteroid. The lipid A species of S. meliloti are modified with very long-chain fatty acids (VLCFAs), which play a central role in bacteroid development. A six-gene cluster was hypothesized to be essential for the biosynthesis of VLCFA-modified lipid A. Previously, two cluster gene products, AcpXL and LpxXL, were found to be essential for S. meliloti lipid A VLCFA biosynthesis. In this paper, we show that the remaining four cluster genes are all involved in lipid A VLCFA biosynthesis. Therefore, we have identified novel gene products involved in the biosynthesis of these unusual lipid modifications. By physiological characterization of the cluster mutant strains, we demonstrate the importance of this gene cluster in the legume symbiosis and for growth in the absence of salt. Bacterial LPS species modified with VLCFAs are substantially less immunogenic than Escherichia coli LPS species, which lack VLCFAs. However, we show that the VLCFA modifications do not suppress the immunogenicity of S. meliloti LPS or affect the ability of S. meliloti to induce fluorescent plant defense molecules within the legume. Because VLCFA-modified lipids are produced by other rhizobia and mammalian pathogens, these findings will also be important in understanding the function and biosynthesis of these unusual fatty acids in diverse bacterial species.

Highlights

  • It was recently determined that the lipid A very long-chain fatty acids (VLCFAs) modification is essential for the symbiosis of Sinorhizobium NGR234 with different types of legume hosts [11], further confirming the importance of identifying the other gene products involved in VLCFA biosynthesis

  • Because the RT-PCR using primers internal to the adhA2XL and lpxXL genes yielded a fragment of 477 bp, this confirmed that the adhA2XL and lpxXL genes constitute the second transcriptional unit in the proposed lipid A VLCFA biosynthesis gene cluster (Fig. 1, A and B)

  • Why Is the Cluster FabZXL Gene Not Essential for Lipid A VLCFA Biosynthesis?—In this study, we identified three novel genes, fabF1XL, fabZXL, and adhA2XL, which are involved in the biosynthesis of VLCFA-modified lipid A in S. meliloti

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Summary

Strain or plasmid

Plasmids pRK600 pk18mobGII pRF771 pSmfabZXL pSmfabF1XL pSmfabF2XL pSmadhA2XL pSmacpXL pSmlpxXL. Smr derivative of SU47 Rm1021 acpXL::pk18mobGII Nmr Rm1021 lpxXL::pJH104 Nmr Hmr Rm1021 adhA2XL::pk18mobGII Nmr Rm1021 fabF1XL::pk18mobGII Nmr Rm1021 fabF2XL::pk18mobGII Nmr Rm1021 fabZXL::pk18mobGII Nmr Rm1021 msbA2::pJH104 Nmr supE44⌬lacU169 (w80lacZDM15) hsdR17 recA1 endA1 gyrA96 thi-1 relA1 MM294A recA56 (pRK600) Cmr pRK2013 npt::Tn9 Cmr mob lacZ␣ gusA Kmr pTE3 with an alternative polylinker TcR pRF771 carrying fabZXL with a 31 bp upstream of the start codon of the gene TcR pRF771 carrying fabF2XL with a 54 bp upstream of the start codon of the gene TcR pRF771 carrying fabF1XL and 31 bp upstream of the start codon of the gene TcR pRF771 carrying adhA2XL and 31 bp upstream of the start codon of the gene TcR pRF771 carrying acpXL and 40 bp upstream of the start codon of the gene TcR pRF771 carrying IpxXL and 33 bp upstream of the start codon of the gene TcR

Source or reference
EXPERIMENTAL PROCEDURES
Primer name
RESULTS
Hydroxylated fatty acids
Class II nodules
DISCUSSION
Full Text
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