Journal of Bacteriology, August 2004, p . 5197-5201, Vol . 186, No . 16

Phosphate Control of the Biosynthesis of Antibiotics and Other Secondary Metabolites Is Mediated by the PhoR-PhoP System: an Unfinished Story

Juan F . Martín^*

Area of Microbiology, University of León, and Institute of Biotechnology, Science Park of León, 24006, León, Spain

 
The biosynthesis of many different types of antibiotics and other secondary metabolites is regulated by phosphate . Production of these valuable compounds occurs only under phosphate-limiting nutritional conditions . In a few cases, there is evidence showing that the negative phosphate control is exerted at the transcriptional level . Recently, it was shown that phosphate control of antibiotic biosynthesis in Streptomyces lividans and Streptomyces coelicolor is mediated by the two-component PhoR-PhoP system that also controls the alkaline phosphatase gene (phoA) . The PhoR protein is a standard membrane sensor kinase, whereas PhoP is a member of the DNA-binding response regulators . In Escherichia coli and Bacillus subtilis, the phosphorylated PhoP protein (PhoPP) activates, in response to phosphate starvation, expression of the pho regulon genes by binding to consensus phosphate boxes in the promoter regions (PHO boxes) . Expression of phoA in S . lividans is induced by PhoPP, and mutants lacking phoP (or phoR and phoP) do not form PhoA . These mutants overproduce large amounts of actinorhodin and undecylprodigiosin . No consensus PHO boxes occur in the upstream region of phosphate-regulated secondary metabolism genes . However, pathway-specific activator proteins (ActII-open reading frame 4 [ORF4], RedD, CcaR, and DnrI) are known to bind to these regions . In S . coelicolor, actII-orf4 is positively regulated by the AfsS protein, which, in turn, is induced by the phosphorylated AfsR protein . It is likely that the PhoR-PhoP system exerts its action on actinorhodin and undecylprodigiosin by a cascade mechanism mediated by AfsR and AfsS . Directed phoR-phoP gene disruption will be very useful for the construction of tailored phosphate-deregulated strains overproducing valuable secondary metabolites .

 
The negative control exerted by inorganic phosphate on the biosynthesis of antibiotics and other secondary metabolites has been known for many years . Over the last four decades, an impressive number of antibiotics and secondary metabolites have been shown to be regulated negatively by phosphate . These include streptomycin, oxytetracycline, clavulanic acid, tylosin, echinomycin, cephalosporin, cephamycin C, and thienamycin, among many other secondary metabolites (23, 27, 32), but, surprisingly, the molecular mechanism of phosphate control has remained obscure (30) in spite of its basic and industrial relevance . It is interesting that inorganic phosphate in the culture medium controls the synthesis of a large number of secondary metabolites belonging to different biosynthetic groups such as, for example, macrolides, tetracyclines, anthracyclines, polyether compounds, aminoglycosides, and amino acid-derived metabolites such as clavulanic acid, among others (10, 11, 15, 16, 25) . Why are all these compounds repressed by high concentrations of inorganic phosphate? From a biosynthetic point of view, these groups of metabolites have very little in common, except that they all are dispensable "secondary" metabolites . The negative effect exerted by inorganic phosphate on the biosynthesis of secondary metabolites is observed in a wide range of microorganisms, including proteobacteria, gram-positive bacteria (e.g., actinomycetes), and filamentous fungi, and probably has a wide ecological role . Martín and Demain proposed that phosphate control is used as a mechanism that triggers secondary metabolite biosynthesis when phosphate in the environment is depleted and, therefore, growth of the microorganisms cannot proceed at a normal rate (28) . When the phosphate concentration in the culture medium decreases below a threshold level, bacteria increase their production of a variety of metabolites that might serve as direct antagonists to other microorganisms (48) or as biochemical cross talk signals (17, 38, 51) to enhance survival under harsh nutritional conditions (26) .

A number of scientific studies published since the 1970s describe the negative effect of high concentrations of phosphate on the production of a variety of secondary metabolites (reviewed in reference 27) . However, most of these reports are basic accounts of the overall phosphate effect on the control of antibiotic production and were made before the gene clusters encoding the biosynthesis of secondary metabolites were sequenced . These early studies were helpful in designing medium composition to avoid phosphate control, thereby favoring the production of secondary metabolites that are expressed at very low levels .

 
The phosphate control signals of antibiotic biosynthesis, i.e., the biochemical intermediates involved in the signal transduction cascade, have long remained largely unknown . These signals appear to be integrated with the inputs produced by other sensors of environmental or nutritional stress, e.g., carbon or nitrogen limitation (7) . Phosphate control of the biosynthesis of secondary metabolites is exerted at the transcriptional and posttranscriptional (antibiotic synthases activity) levels (reviewed in references 23 and 30) . In at least two cases, it is clearly established that phosphate control of the biosynthesis of the secondary metabolites candicidin and oxytetracycline is exerted at the transcriptional level (3, 34) . Expression of the pabS gene of S . griseus, which encodes the candicidin precursor-forming enzyme p-aminobenzoic acid (PABA) synthase (3), and expression of the tetracycline biosynthesis genes otcC, otcX, and otcY (34) are observed only under phosphate-limiting conditions . otcC encodes anhydrotetracycline oxygenase, and otcY codes for the tetracycline polyketide synthase, whereas otcX is a gene divergent to otcC encoding a protein of unknown function (19) .

The more advanced studies on phosphate control of secondary metabolites have been done with the model actinomycetes S . coelicolor and S . lividans (11, 16) . The synthesis of the S . coelicolor pigmented secondary metabolites actinorhodin and undecylprodigiosin is also negatively controlled by high phosphate concentrations (11, 16) . Actinorhodin is synthesized by a type II polyketide synthetase, whereas undecylprodigiosin is a pyrrolic compound derived from proline . Surprisingly, no transcriptional studies were available until recently (see below) on the molecular mechanism of phosphate control of the expression of the actinorhodin and undecylprodigiosin genes .

Genes encoding secondary metabolites are frequently linked in clusters (5, 29) . Phosphate control appears to repress the expression of entire clusters of antibiotic biosynthesis genes, e.g., genes encoding the activating enzyme PABA-coenzyme A ligase and a thioesterase, in addition to PABA synthase in the candicidin gene cluster (6, 9) or the complete pimaricin gene cluster (2) . A question that remains unanswered is whether each promoter corresponding to phosphate-sensitive genes contains a phosphate box or whether there is a master gene encoding a regulatory protein involved in the activation of antibiotic biosynthetic genes that in turn is controlled by the inorganic phosphate level .

 
In E . coli and B . subtilis, about 30 genes belonging to the pho regulon are controlled by the two-component PhoR-PhoB (named PhoR-PhoP in B . subtilis) system (18, 46) . More genes of the pho regulon have been identified by proteomics and transcriptional studies of B . subtilis (1) and by microarray analysis of Corynebacterium glutamicum (21) .

In E . coli, the sensor protein kinase PhoR self-phosphorylates under conditions of phosphate starvation (forming PhoRP) that transfers its phosphate group to the dephosphorylated PhoB . The phosphorylated PhoB activates expression of about 30 phosphate-regulated genes by binding to the PHO boxes located in the 5' region of these genes (46) . Expression of phoA and other members of the phosphate regulon takes place under phosphate-limiting conditions when the PhoB transcriptional activator is available in its phosphorylated form (PhoBP) . The mechanism is essentially identical in B . subtilis (18, 40) . PHO boxes in E . coli consist of 18 nucleotides (C/T)TGTCATA(A/T)A(A/T)CTGTCA(T/C) formed by two direct repeats of 7 nucleotides (C/T)TGTCAT separated by four adenines or thymines . This sequence has been found, with minor changes, in the promoters of a variety of phosphate-controlled genes in different proteobacteria (30, 46) (Fig. 1) .

 
Similar PHO boxes, although with a different consensus sequence, occur in B . subtilis . Each box consists of two hexanucleotides [TT(A/T)ACA] repeated in tandem and separated by three to seven nucleotides (24), in contrast to E . coli, for which the separation of the two repeats in each PHO box is always of four nucleotides (Fig . 1) .

The full genome sequence of S . coelicolor (4) and S . avermitilis (20, 39) is now available, and some others will soon be accessible . Several research groups have provided evidence showing that the production of methylenomycin, actinorhodin, and undecylprodigiosin in cultures of S . coelicolor is reduced by high phosphate concentrations (11, 16) . Until a few years ago, it was unclear whether standard PHO boxes might occur in the upstream regions of antibiotic biosynthesis genes (23) . However, repeated searches to find standard PHO boxes in the upstream region of act (for actinorhodin) or red (for undecylprodigiosin) genes have been unsuccessful . Similarly, no consensus PHO boxes have been found in the upstream region of the phosphate-regulated ppk gene of S . lividans (8) .

Expression of the act and red genes is regulated by the specific transcriptional activators ActII-ORF4 (12, 14) and RedD (37, 44) . Similarly, expression of the daunorubicin gene cluster in Streptomyces peucetius is controlled by the transcriptional activator DnrI (45) . The activator proteins ActII-ORF4, RedD, DnrI, and other pathway-specific regulators, such as CcaR in Streptomyces clavuligerus (41), belong to the group of SARP (Streptomyces antibiotic regulatory protein) regulators (50) that form part of the OmpR superfamily (31, 35, 41) . It is possible that the expression of the transcriptional activators ActII-ORF4 and RedD is controlled by phosphate, but again, the upstream regions of these genes lack classical PHO boxes . Initial evidence suggests, however, that the phosphate effect is mediated by a different sequence in the GC-rich promoters of Streptomyces species than in E . coli .

 
After the cloning and characterization of the extracellular alkaline phosphatase (phoA) gene of S . griseus (36), we found three putative phosphatase genes in the S . coelicolor genome . One of them, phoA (the putative extracellular alkaline phosphatase gene) showed 71% identity to S . griseus phoA, identified unequivocally by sequencing of the amino-terminal end of the purified extracellular alkaline phosphatase (36) . The biochemical characteristics of PhoB are unknown and PhoC corresponds to a phosphodiesterase .

Recently, the phoR-phoP systems of S . coelicolor and S . lividans were cloned, and their role in actinorhodin and undecylprodigiosin biosynthesis in S . lividans was studied by gene disruption and gene replacement (43) . The phoR-phoP cluster has also been identified and disrupted in the S . avermitilis genome (H . Ikeda, J . F . Martín, and S . Omura, unpublished data) . In Streptomyces species, PhoR shows all of the characteristics of a transmembrane sensor protein, whereas PhoP is a member of the DNA-binding OmpR family (35) . PhoR (426 amino acids; 45.4 kDa in S . coelicolor) has two hydrophobic, membrane-spanning regions in the N-terminal domain and a large extramembrane domain that may serve as a sensor of environmental signals (35, 43) . In B . subtilis the cytoplasmic kinase domain of PhoR is sufficient for the low phosphate expression of the pho regulon genes (42) . The S . coelicolor and S . lividans 24.7-kDa PhoP protein belonging to the OmpR family contains a DNA-binding domain in the carboxyl-terminal region (residues 190 to 201) (43) .

The S . lividans phoR-phoP deletion mutants (named phoP and phoRP) lacking either PhoP or both PhoR and PhoP proteins are unable to synthesize extracellular alkaline phosphatase, as shown by Western blot analysis . The formation of alkaline phosphatase was restored by complementation of the deletion mutants with phoR-phoP, confirming the involvement (positive effect) of the two-component system in the phosphate control of phoA in this actinomycete (43) . A very interesting finding is the observation that mutants with phoR-phoP deletions overproduce large amounts of actinorhodin and undecylprodigiosin in a manner that is partially insensitive to phosphate (1 to 10 mM) control .

Phosphate control of the biosynthesis of actinorhodin and undecylprodigiosin was restored by complementation of the pho mutants with the phoR-phoP cluster (43) . These results clearly indicate that expression of either primary metabolism genes such as phoA or genes involved in the biosynthesis of secondary metabolites such as actinorhodin and undecylprodigiosin are under the phosphate control mechanism mediated by PhoR-PhoP .

 
It is possible that there is a phosphate control mechanism of antibiotic gene expression different from that recognizing the classical PHO box sequences . It is important to note that, whereas PhoP exerts a positive regulation on expression of the phoA gene, as occurs in other bacteria, expression of S . lividans or S . coelicolor pigments and antibiotics is regulated negatively, i.e., inactivation of the response regulator PhoP or deletion of the entire PhoR-PhoP system results in overexpression of actinorhodin and undecylprodigiosin . This suggests that the modes of regulation of the alkaline phosphatase and secondary metabolite genes are different and that the PhoR-PhoP action on antibiotic gene expression may be mediated through other DNA-binding proteins, e.g., pathway-specific regulators .

In S . lividans and S . coelicolor, there is a small (63-amino-acid) protein, AfsS, encoded by a short ORF located in the 3' region immediately downstream of the regulatory gene AfsR . AfsS is a rare protein (thus far, it is found only in a few Streptomyces species) that contains three repeats of the 11-amino-acid sequence TXXDHMPXXPA (where X represents any amino acid) (33) . Overexpression of AfsS in S . lividans (or S . coelicolor) leads to an overproduction of actinorhodin and undecylprodigiosin, even in mutants disrupted in AfsR . Recently, Lee et al . (22) have shown that the afsS gene is the target for the AfsR regulator, a widespread transcription factor that has ATPase activity (47) . S . lividans has an afsS analogue named afsR2 (49) . Floriano and Bibb (13) reported that AfsS protein stimulates the production of actinorhodin by enhancing the transcription of the pathway-specific regulator ActII-ORF4 and that the same occurs in S . lividans when afsR2 was overexpressed .

A possible cascade mechanism involves a negative effect of phosphorylated PhoP on the expression of afsS, resulting in downregulation of actII-ORF4 and redD expression (Fig . 2) . Due to their low concentration, ActII-ORF4 and RedD would be unable to induce the actinorhodin and undecylprodigiosin biosynthetic genes . Null phoR-phoP mutants lack the PhoP response regulator and therefore would be unable to repress the afs gene, leading to constitutive formation of AfsS, resulting in induction of actII-ORF4 and redD and finally in actinorhodin and undecylprodigiosin overproduction .

 
The recent identification of a large number of structural and regulatory genes involved in antibiotic biosynthesis permits analysis of the mechanism of PhoR-PhoP-mediated global control in other Streptomyces species, some of which produce antibiotics, antitumor agents, immunosuppressants, and many other biologically active compounds of high commercial interest . In all of these cases, phosphate represses the biosynthesis of these compounds, and a proper understanding of the control mechanism in these actinomycetes will allow targeted derepression of antibiotic production .

 
This work was supported by a grant from the Ministry of Education and Science of Spain CICYT Bio2003 01489) .

I thank P . Liras, A . Sola, and A . Rodriguez for valuable discussions .

 
* Mailing address: Area of Microbiology, University of León, 24006, León, Spain . Phone: 34-987-291-506 . Fax: 34-987-291-506 . E-mail: degjmm@unileon.es .

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