Recent advances in understanding Streptomyces

About 2,500 papers dated 2014–2016 were recovered by searching the PubMed database for Streptomyces, which are the richest known source of antibiotics. This review integrates around 100 of these papers in sections dealing with evolution, ecology, pathogenicity, growth and development, stress responses and secondary metabolism, gene expression, and technical advances. Genomic approaches have greatly accelerated progress. For example, it has been definitively shown that interspecies recombination of conserved genes has occurred during evolution, in addition to exchanges of some of the tens of thousands of non-conserved accessory genes. The closeness of the association of Streptomyces with plants, fungi, and insects has become clear and is reflected in the importance of regulators of cellulose and chitin utilisation in overall Streptomyces biology. Interestingly, endogenous cellulose-like glycans are also proving important in hyphal growth and in the clumping that affects industrial fermentations. Nucleotide secondary messengers, including cyclic di-GMP, have been shown to provide key input into developmental processes such as germination and reproductive growth, while late morphological changes during sporulation involve control by phosphorylation. The discovery that nitric oxide is produced endogenously puts a new face on speculative models in which regulatory Wbl proteins (peculiar to actinobacteria) respond to nitric oxide produced in stressful physiological transitions. Some dramatic insights have come from a new model system for Streptomyces developmental biology, Streptomyces venezuelae, including molecular evidence of very close interplay in each of two pairs of regulatory proteins. An extra dimension has been added to the many complexities of the regulation of secondary metabolism by findings of regulatory crosstalk within and between pathways, and even between species, mediated by end products. Among many outcomes from the application of chromosome immunoprecipitation sequencing (ChIP-seq) analysis and other methods based on “next-generation sequencing” has been the finding that 21% of Streptomyces mRNA species lack leader sequences and conventional ribosome binding sites. Further technical advances now emerging should lead to continued acceleration of knowledge, and more effective exploitation, of these astonishing and critically important organisms.

[1]  M. Buttner,et al.  Identification and Characterization of CdgB, a Diguanylate Cyclase Involved in Developmental Processes in Streptomyces coelicolor , 2011, Journal of bacteriology.

[2]  Shiyun Chen,et al.  Mycobacterial WhiB6 Differentially Regulates ESX-1 and the Dos Regulon to Modulate Granuloma Formation and Virulence in Zebrafish. , 2016, Cell reports.

[3]  S. Bornemann,et al.  Developmental delay in a Streptomyces venezuelae glgE null mutant is associated with the accumulation of α-maltose 1-phosphate , 2016, Microbiology.

[4]  K. Chater,et al.  The use of the rare UUA codon to define “Expression Space” for genes involved in secondary metabolism, development and environmental adaptation in Streptomyces , 2008, The Journal of Microbiology.

[5]  J. Maupin-Furlow Prokaryotic ubiquitin-like protein modification. , 2014, Annual review of microbiology.

[6]  J. F. Aparicio,et al.  Pathway-specific regulation revisited: cross-regulation of multiple disparate gene clusters by PAS-LuxR transcriptional regulators , 2015, Applied Microbiology and Biotechnology.

[7]  P. Mackiewicz,et al.  ParA and ParB coordinate chromosome segregation with cell elongation and division during Streptomyces sporulation , 2016, Open Biology.

[8]  J. Zakrzewska‐Czerwińska,et al.  Two transcription factors, CabA and CabR, are independently involved in multilevel regulation of the biosynthetic gene cluster encoding the novel aminocoumarin, cacibiocin , 2015, Applied Microbiology and Biotechnology.

[9]  J. Badger,et al.  Genome Content and Phylogenomics Reveal both Ancestral and Lateral Evolutionary Pathways in Plant-Pathogenic Streptomyces Species , 2016, Applied and Environmental Microbiology.

[10]  Jason C. Crack,et al.  Nitrosylation of Nitric‐Oxide‐Sensing Regulatory Proteins Containing [4Fe‐4S] Clusters Gives Rise to Multiple Iron–Nitrosyl Complexes , 2016, Angewandte Chemie.

[11]  K. Chater,et al.  Developmental biology of Streptomyces from the perspective of 100 actinobacterial genome sequences , 2013, FEMS microbiology reviews.

[12]  K. Chater,et al.  Specialised metabolites regulating antibiotic biosynthesis in Streptomyces spp. , 2016, FEMS microbiology reviews.

[13]  E. Monga,et al.  Morphological, Physiological, and Taxonomic Characterization of Actinobacterial Isolates Living as Endophytes of Cacao Pods and Cacao Seeds , 2016, Microbes and environments.

[14]  Ying Huang,et al.  Widespread interspecies homologous recombination reveals reticulate evolution within the genus Streptomyces. , 2016, Molecular phylogenetics and evolution.

[15]  K. Gindro,et al.  Metabolite induction via microorganism co-culture: a potential way to enhance chemical diversity for drug discovery. , 2014, Biotechnology advances.

[16]  Divya Vasudevan,et al.  Nitric oxide, the new architect of epigenetic landscapes. , 2016, Nitric oxide : biology and chemistry.

[17]  Yinhua Lu,et al.  Cross-talk between an orphan response regulator and a noncognate histidine kinase in Streptomyces coelicolor. , 2009, FEMS microbiology letters.

[18]  Xingxing Li,et al.  Binding of a biosynthetic intermediate to AtrA modulates the production of lidamycin by Streptomyces globisporus , 2015, Molecular microbiology.

[19]  G. Muth,et al.  The conjugative DNA-transfer apparatus of Streptomyces. , 2015, International journal of medical microbiology : IJMM.

[20]  Mark T. Gladwin,et al.  The nitrate–nitrite–nitric oxide pathway in physiology and therapeutics , 2008, Nature Reviews Drug Discovery.

[21]  S. Goormachtig,et al.  Streptomyces as a plant's best friend? , 2016, FEMS microbiology ecology.

[22]  M. Buttner,et al.  WhiD and WhiB, Homologous Proteins Required for Different Stages of Sporulation in Streptomyces coelicolor A3(2) , 2000, Journal of bacteriology.

[23]  Li-rong Han,et al.  Effects of Plant Stress Signal Molecules on the Production of Wilforgine in an Endophytic Actinomycete Isolated from Tripterygium wilfordii Hook.f. , 2015, Current Microbiology.

[24]  Gang Liu,et al.  Molecular Regulation of Antibiotic Biosynthesis in Streptomyces , 2013, Microbiology and Molecular Reviews.

[25]  Shiwei Wang,et al.  An Active Type I-E CRISPR-Cas System Identified in Streptomyces avermitilis , 2016, PloS one.

[26]  G. Muth,et al.  Fluorescence microscopy of Streptomyces conjugation suggests DNA-transfer at the lateral walls and reveals the spreading of the plasmid in the recipient mycelium. , 2016, Environmental microbiology.

[27]  Ju-Hyeon Lim,et al.  Molecular characterization of Streptomyces coelicolor A(3) SCO6548 as a cellulose 1,4-β-cellobiosidase. , 2016, FEMS microbiology letters.

[28]  D. Homerova,et al.  The σ(F)-specific anti-sigma factor RsfA is one of the protein kinases that phosphorylates the pleiotropic anti-anti-sigma factor BldG in Streptomyces coelicolor A3(2). , 2014, Gene.

[29]  M. Bernards,et al.  Suberin Regulates the Production of Cellulolytic Enzymes in Streptomyces scabiei, the Causal Agent of Potato Common Scab , 2015, Microbes and environments.

[30]  S. Rigali,et al.  The Cellobiose Sensor CebR Is the Gatekeeper of Streptomyces scabies Pathogenicity , 2015, mBio.

[31]  K. Ochi,et al.  Lincomycin at Subinhibitory Concentrations Potentiates Secondary Metabolite Production by Streptomyces spp , 2015, Applied and Environmental Microbiology.

[32]  S. Brady,et al.  Global biogeographic sampling of bacterial secondary metabolism , 2015, eLife.

[33]  Yinhua Lu,et al.  One-step high-efficiency CRISPR/Cas9-mediated genome editing in Streptomyces. , 2015, Acta biochimica et biophysica Sinica.

[34]  Michael S. Fernandopulle,et al.  Genetic and Proteomic Analyses of Pupylation in Streptomyces coelicolor , 2015, Journal of bacteriology.

[35]  R. Loria,et al.  Characterization of the Integration and Modular Excision of the Integrative Conjugative Element PAISt in Streptomyces turgidiscabies Car8 , 2014, PloS one.

[36]  J. Kalinowski,et al.  Complete genome sequence of Streptomyces reticuli, an efficient degrader of crystalline cellulose. , 2016, Journal of biotechnology.

[37]  K. Chater,et al.  Importance and regulation of inositol biosynthesis during growth and differentiation of Streptomyces , 2012, Molecular microbiology.

[38]  Jason C. Crack,et al.  NsrR from Streptomyces coelicolor Is a Nitric Oxide-sensing [4Fe-4S] Cluster Protein with a Specialized Regulatory Function* , 2015, The Journal of Biological Chemistry.

[39]  Dennis Claessen,et al.  A novel locus for mycelial aggregation forms a gateway to improved Streptomyces cell factories , 2015, Microbial Cell Factories.

[40]  Henry J. Haiser,et al.  Nucleotide Second Messenger‐Mediated Regulation of a Muralytic Enzyme in Streptomyces , 2015, Molecular microbiology.

[41]  Daniel M. Cornforth,et al.  Antibiotics and the art of bacterial war , 2015, Proceedings of the National Academy of Sciences.

[42]  Sean F. Brady,et al.  Chemical-biogeographic survey of secondary metabolism in soil , 2014, Proceedings of the National Academy of Sciences.

[43]  Henry J. Haiser,et al.  Resuscitation-Promoting Factors Are Cell Wall-Lytic Enzymes with Important Roles in the Germination and Growth of Streptomyces coelicolor , 2014, Journal of bacteriology.

[44]  Byung-Kwan Cho,et al.  Genome-scale analysis reveals a role for NdgR in the thiol oxidative stress response in Streptomyces coelicolor , 2015, BMC Genomics.

[45]  V. Burrus,et al.  Identification of genetic and environmental factors stimulating excision from Streptomyces scabiei chromosome of the toxicogenic region responsible for pathogenicity. , 2016, Molecular plant pathology.

[46]  D. Hopwood,et al.  Streptomyces in nature and medicine : the antibiotic makers , 2007 .

[47]  S. Horinouchi,et al.  Signalling early developmental events in two highly diverged Streptomyces species , 2003, Molecular microbiology.

[48]  R. Kolter,et al.  Natural products in soil microbe interactions and evolution. , 2015, Natural product reports.

[49]  Juan Wang,et al.  “Pseudo” γ-Butyrolactone Receptors Respond to Antibiotic Signals to Coordinate Antibiotic Biosynthesis* , 2010, Journal of Biological Chemistry.

[50]  C. Nathan,et al.  Nitrite impacts the survival of Mycobacterium tuberculosis in response to isoniazid and hydrogen peroxide , 2013, MicrobiologyOpen.

[51]  M. Elliot,et al.  Complex Intra-Operonic Dynamics Mediated by a Small RNA in Streptomyces coelicolor , 2014, PloS one.

[52]  T. Schäberle,et al.  Enhanced production of undecylprodigiosin in Streptomyces coelicolor by co-cultivation with the corallopyronin A-producing myxobacterium, Corallococcus coralloides , 2014, Biotechnology Letters.

[53]  S. Jensen Biosynthesis of clavam metabolites , 2012, Journal of Industrial Microbiology & Biotechnology.

[54]  K. Fan,et al.  Genome-wide identification and characterization of reference genes with different transcript abundances for Streptomyces coelicolor , 2015, Scientific Reports.

[55]  G. Niu,et al.  A γ‐butyrolactone‐sensing activator/repressor, JadR3, controls a regulatory mini‐network for jadomycin biosynthesis , 2014, Molecular microbiology.

[56]  V. Gupta,et al.  Detection of biosynthetic gene and phytohormone production by endophytic actinobacteria associated with Solanum lycopersicum and their plant-growth-promoting effect. , 2016, Research in microbiology.

[57]  K. Tahlan,et al.  Regulation of Coronafacoyl Phytotoxin Production by the PAS-LuxR Family Regulator CfaR in the Common Scab Pathogen Streptomyces scabies , 2015, PloS one.

[58]  Rainer Breitling,et al.  Synthetic Biology of Natural Products. , 2016, Cold Spring Harbor perspectives in biology.

[59]  Yaojun Tong,et al.  CRISPR-Cas9 Based Engineering of Actinomycetal Genomes. , 2015, ACS synthetic biology.

[60]  Satyendra P. Singh,et al.  Evaluation of antagonistic and plant growth promoting activities of chitinolytic endophytic actinomycetes associated with medicinal plants against Sclerotium rolfsii in chickpea , 2016, Journal of applied microbiology.

[61]  Cheryl P. Andam,et al.  A Latitudinal Diversity Gradient in Terrestrial Bacteria of the Genus Streptomyces , 2016, mBio.

[62]  M. Watve,et al.  Widespread predatory abilities in the genus Streptomyces , 2014, Archives of Microbiology.

[63]  Don D. Nguyen,et al.  Plasticity of Streptomyces coelicolor Membrane Composition Under Different Growth Conditions and During Development , 2015, Front. Microbiol..

[64]  Taichi E. Takasuka,et al.  Evolution of High Cellulolytic Activity in Symbiotic Streptomyces through Selection of Expanded Gene Content and Coordinated Gene Expression , 2016, PLoS biology.

[65]  Weishan Wang,et al.  ScbR- and ScbR2-mediated signal transduction networks coordinate complex physiological responses in Streptomyces coelicolor , 2015, Scientific Reports.

[66]  G. Niu,et al.  Genome engineering and direct cloning of antibiotic gene clusters via phage ϕBT1 integrase-mediated site-specific recombination in Streptomyces , 2015, Scientific Reports.

[67]  Á. Manteca,et al.  New insights on the development of Streptomyces and their relationships with secondary metabolite production. , 2012, Current trends in microbiology.

[68]  Klas Flärdh,et al.  c-di-GMP signalling and the regulation of developmental transitions in streptomycetes , 2015, Nature Reviews Microbiology.

[69]  J. Worrall,et al.  GlxA is a new structural member of the radical copper oxidase family and is required for glycan deposition at hyphal tips and morphogenesis of Streptomyces lividans. , 2015, The Biochemical journal.

[70]  Xiaolin Li,et al.  Endophytic Streptomyces sp. Y3111 from traditional Chinese medicine produced antitubercular pluramycins , 2014, Applied Microbiology and Biotechnology.

[71]  J. Seger,et al.  Partner choice and fidelity stabilize coevolution in a Cretaceous-age defensive symbiosis , 2014, Proceedings of the National Academy of Sciences.

[72]  R. Gadzała-Kopciuch,et al.  Synthesis of siderophores by plant-associated metallotolerant bacteria under exposure to Cd(2.). , 2016, Chemosphere.

[73]  Jason C. Crack,et al.  Differentiated, Promoter-specific Response of [4Fe-4S] NsrR DNA Binding to Reaction with Nitric Oxide* , 2016, The Journal of Biological Chemistry.

[74]  X. Mao,et al.  Sigma factor WhiGch positively regulates natamycin production in Streptomyces chattanoogensis L10 , 2015, Applied Microbiology and Biotechnology.

[75]  Jason C. Crack,et al.  Iron-sulfur clusters as biological sensors: the chemistry of reactions with molecular oxygen and nitric oxide. , 2014, Accounts of chemical research.

[76]  K. Chater,et al.  Unexpected and widespread connections between bacterial glycogen and trehalose metabolism. , 2011, Microbiology.

[77]  R. Seipke Strain-Level Diversity of Secondary Metabolism in Streptomyces albus , 2015, PloS one.

[78]  Genome Update. Let the consumer beware: Streptomyces genome sequence quality , 2016, Microbial biotechnology.

[79]  R. Sawers,et al.  Oxygen-Dependent Control of Respiratory Nitrate Reduction in Mycelium of Streptomyces coelicolor A3(2) , 2014, Journal of bacteriology.

[80]  J. Willemse,et al.  Cross-membranes orchestrate compartmentalization and morphogenesis in Streptomyces , 2016, Nature Communications.

[81]  Kai Blin,et al.  antiSMASH 3.0—a comprehensive resource for the genome mining of biosynthetic gene clusters , 2015, Nucleic Acids Res..

[82]  K. Chater,et al.  Evolutionary flux of potentially bldA-dependent Streptomyces genes containing the rare leucine codon TTA , 2008, Antonie van Leeuwenhoek.

[83]  J. Nodwell Are you talking to me? A possible role for γ‐butyrolactones in interspecies signalling , 2014, Molecular microbiology.

[84]  Mark J. Buttner,et al.  Tetrameric c-di-GMP Mediates Effective Transcription Factor Dimerization to Control Streptomyces Development , 2014, Cell.

[85]  K. Lou,et al.  Isolation, Characterization, and Insecticidal Activity of an Endophyte of Drunken Horse Grass, Achnatherum inebrians , 2013, Journal of insect science.

[86]  J. Willemse,et al.  Aggregation of germlings is a major contributing factor towards mycelial heterogeneity of Streptomyces , 2016, Scientific Reports.

[87]  A. Omirbekova,et al.  Bacterial endophytes of Trans-Ili Alatau region's plants as promising components of a microbial preparation for agricultural use. , 2016, Acta biochimica Polonica.

[88]  Huimin Zhao,et al.  Systematic Identification of a Panel of Strong Constitutive Promoters from Streptomyces albus. , 2015, ACS synthetic biology.

[89]  Klas Flärdh,et al.  Fluorescence Time-lapse Imaging of the Complete S. venezuelae Life Cycle Using a Microfluidic Device , 2016, Journal of visualized experiments : JoVE.

[90]  Byung-Kwan Cho,et al.  Comparative Genomics Reveals the Core and Accessory Genomes of Streptomyces Species. , 2015, Journal of microbiology and biotechnology.

[91]  W. Hinrichs,et al.  Structure and regulatory targets of SCO3201, a highly promiscuous TetR-like regulator of Streptomyces coelicolor M145. , 2014, Biochemical and biophysical research communications.

[92]  M. Kaltenpoth,et al.  Streptomyces as symbionts: an emerging and widespread theme? , 2012, FEMS microbiology reviews.

[93]  Yunkun Liu,et al.  In Vitro CRISPR/Cas9 System for Efficient Targeted DNA Editing , 2015, mBio.

[94]  J. Martiny History Leaves Its Mark on Soil Bacterial Diversity , 2016, mBio.

[95]  H. Ikeda,et al.  Nitrogen oxide cycle regulates nitric oxide levels and bacterial cell signaling , 2016, Scientific Reports.

[96]  M. Gelfand,et al.  Genomics of Sponge-Associated Streptomyces spp. Closely Related to Streptomyces albus J1074: Insights into Marine Adaptation and Secondary Metabolite Biosynthesis Potential , 2014, PloS one.

[97]  K. Kristiansen,et al.  Activation of chloramphenicol biosynthesis in Streptomyces venezuelae ATCC 10712 by ethanol shock: insights from the promoter fusion studies , 2016, Microbial Cell Factories.

[98]  Renduo Zhang,et al.  Illumina-based analysis of core actinobacteriome in roots, stems, and grains of rice. , 2016, Microbiological research.

[99]  M. Díaz,et al.  The two kinases, AbrC1 and AbrC2, of the atypical two-component system AbrC are needed to regulate antibiotic production and differentiation in Streptomyces coelicolor , 2015, Front. Microbiol..

[100]  Natalia Tschowri Cyclic Dinucleotide-Controlled Regulatory Pathways in Streptomyces Species , 2015, Journal of bacteriology.

[101]  C. Nathan,et al.  Nitrite produced by Mycobacterium tuberculosis in human macrophages in physiologic oxygen impacts bacterial ATP consumption and gene expression , 2013, Proceedings of the National Academy of Sciences.

[102]  P. Straight,et al.  Bacterial Competition Reveals Differential Regulation of the pks Genes by Bacillus subtilis , 2013, Journal of bacteriology.

[103]  M. Díaz,et al.  Toward a new focus in antibiotic and drug discovery from the Streptomyces arsenal , 2015, Front. Microbiol..

[104]  A. M. Caraballo-Rodríguez,et al.  Endophytic Actinobacteria from the Brazilian Medicinal Plant Lychnophora ericoides Mart. and the Biological Potential of Their Secondary Metabolites , 2016, Chemistry & biodiversity.

[105]  R. Brzezinski,et al.  Uptake of chitosan-derived D-glucosamine oligosaccharides in Streptomyces coelicolor A3(2). , 2015, FEMS microbiology letters.

[106]  J. Willemse,et al.  Subcompartmentalization by cross-membranes during early growth of Streptomyces hyphae , 2016, Nature Communications.

[107]  G. V. van Wezel,et al.  Multiple allosteric effectors control the affinity of DasR for its target sites. , 2015, Biochemical and biophysical research communications.

[108]  K. Chater,et al.  The positions of the sigma‐factor genes, whiG and sigF, in the hierarchy controlling the development of spore chains in the aerial hyphae of Streptomyces coelicolor A3(2) , 1996, Molecular microbiology.

[109]  O. Benada,et al.  The Absence of Pupylation (Prokaryotic Ubiquitin-Like Protein Modification) Affects Morphological and Physiological Differentiation in Streptomyces coelicolor , 2015, Journal of bacteriology.

[110]  Björn Sohlberg,et al.  Cross‐regulation among disparate antibiotic biosynthetic pathways of Streptomyces coelicolor , 2005, Molecular microbiology.

[111]  M. Buttner,et al.  Genome-Wide Chromatin Immunoprecipitation Sequencing Analysis Shows that WhiB Is a Transcription Factor That Cocontrols Its Regulon with WhiA To Initiate Developmental Cell Division in Streptomyces , 2016, mBio.

[112]  Antje M. Hempel,et al.  Regulation of apical growth and hyphal branching in Streptomyces. , 2012, Current opinion in microbiology.

[113]  Alissa S. Hanshew,et al.  Characterization of Actinobacteria Associated with Three Ant–Plant Mutualisms , 2014, Microbial Ecology.

[114]  X. Mao,et al.  Proteasome involvement in a complex cascade mediating SigT degradation during differentiation of Streptomyces coelicolor , 2014, FEBS letters.

[115]  D. Worthen Streptomyces in Nature and Medicine: The Antibiotic Makers (review) , 2007 .

[116]  M. Buttner,et al.  Response Regulator Heterodimer Formation Controls a Key Stage in Streptomyces Development , 2014, PLoS genetics.

[117]  K. Fan,et al.  Angucyclines as signals modulate the behaviors of Streptomyces coelicolor , 2014, Proceedings of the National Academy of Sciences.

[118]  I. Grosse,et al.  Streptomyces-induced resistance against oak powdery mildew involves host plant responses in defense, photosynthesis, and secondary metabolism pathways. , 2014, Molecular plant-microbe interactions : MPMI.

[119]  Jeffrey Green,et al.  Transcriptional regulation of bacterial virulence gene expression by molecular oxygen and nitric oxide , 2014, Virulence.

[120]  Richard H. Baltz,et al.  Genetic manipulation of secondary metabolite biosynthesis for improved production in Streptomyces and other actinomycetes , 2016, Journal of Industrial Microbiology & Biotechnology.

[121]  D. Buckley,et al.  Widespread homologous recombination within and between Streptomyces species , 2010, The ISME Journal.

[122]  Zixin Deng,et al.  Highly efficient editing of the actinorhodin polyketide chain length factor gene in Streptomyces coelicolor M145 using CRISPR/Cas9-CodA(sm) combined system , 2015, Applied Microbiology and Biotechnology.

[123]  G. V. van Wezel,et al.  Socially mediated induction and suppression of antibiosis during bacterial coexistence , 2015, Proceedings of the National Academy of Sciences.

[124]  Min Woo Kim,et al.  The dynamic transcriptional and translational landscape of the model antibiotic producer Streptomyces coelicolor A3(2) , 2016, Nature Communications.

[125]  P. Dyson,et al.  A Laterally Acquired Galactose Oxidase-Like Gene Is Required for Aerial Development during Osmotic Stress in Streptomyces coelicolor , 2013, PloS one.

[126]  Tracy Palmer,et al.  The complex extracellular biology of Streptomyces. , 2010, FEMS microbiology reviews.

[127]  G. V. van Wezel,et al.  Genome-Wide Analysis of In Vivo Binding of the Master Regulator DasR in Streptomyces coelicolor Identifies Novel Non-Canonical Targets , 2015, PloS one.

[128]  R. Loria,et al.  Thaxtomin A production and virulence are controlled by several bld gene global regulators in Streptomyces scabies. , 2014, Molecular plant-microbe interactions : MPMI.

[129]  J. Willemse,et al.  Positive control of cell division: FtsZ is recruited by SsgB during sporulation of Streptomyces. , 2011, Genes & development.

[130]  Camilo F. Martinez-Farina,et al.  JadX is a Disparate Natural Product Binding Protein. , 2016, Journal of the American Chemical Society.

[131]  P. Cortesi,et al.  Biological Control of Lettuce Drop and Host Plant Colonization by Rhizospheric and Endophytic Streptomycetes , 2016, Front. Microbiol..

[132]  G. Bucca,et al.  Deciphering the Regulon of Streptomyces coelicolor AbrC3, a Positive Response Regulator of Antibiotic Production , 2014, Applied and Environmental Microbiology.

[133]  J. Willemse,et al.  SepG coordinates sporulation-specific cell division and nucleoid organization in Streptomyces coelicolor , 2016, Open Biology.

[134]  Lourdes Peña-Castillo,et al.  Proteomics analysis of global regulatory cascades involved in clavulanic acid production and morphological development in Streptomyces clavuligerus , 2016, Journal of Industrial Microbiology & Biotechnology.

[135]  G. V. van Wezel,et al.  Taxonomy, Physiology, and Natural Products of Actinobacteria , 2015, Microbiology and Molecular Reviews.

[136]  H. Tan,et al.  Coordinative Modulation of Chlorothricin Biosynthesis by Binding of the Glycosylated Intermediates and End Product to a Responsive Regulator ChlF1* , 2016, The Journal of Biological Chemistry.

[137]  K. Forchhammer,et al.  DNA affinity capturing identifies new regulators of the heterologously expressed novobiocin gene cluster in Streptomyces coelicolor M512 , 2016, Applied Microbiology and Biotechnology.

[138]  B. Maček,et al.  Control of Morphological Differentiation of Streptomyces coelicolor A3(2) by Phosphorylation of MreC and PBP2 , 2015, PloS one.