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Production of actinorhodin-related "blue pigments" by Streptomyces coelicolor A3(2)
Open accessAbstract
The genetically well-known strain Streptomyces coelicolor A3(2) produces the pH indicator (red/blue) antibiotic actinorhodin, but not all the "blue pigment" produced by this strain is actinorhodin. When the organism was subjected to various nutrient limitations (ammonium, nitrate, phosphate, or trace elements), and also during growth cessation caused by a relatively low medium pH, blue pigment production was initiated but the pigment and its location varied. At pH 4.5 to 5.5, significant formation of actinorhodin occurred and was located exclusively intracellularly. At pH 6.0 to 7.5 a different blue pigment was produced intracellularly as well as extracellularly. It was purified and identified as gamma-actinorhodin (the lactone form of actinorhodin). Analysis of act mutants of S. coelicolor A3(2) confirmed that both pigments are derived from the act biosynthetic pathway. Mutants with lesions in actII-ORF2, actII-ORF3, or actVA-ORF1, previously implicated or suggested to be involved in actinorhodin export, were impaired in production of gamma-actinorhodin, suggesting that synthesis of gamma-actinorhodin from actinorhodin is coupled to its export from the cell. However, effects on the level of actinorhodin production were also found in some mutants.
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TL;DR
Streptomyces coelicolor A3(2) produces a second blue pigment besides actinorhodin, identified as gamma-actinorhodin (the lactone form of actinorhodin), whose production and cellular location depend on nutrient limitation and medium pH. Mutants in genes previously implicated in actinorhodin export were impaired in gamma-actinorhodin production, suggesting its synthesis from actinorhodin is coupled to export.
Key findings
- Under various nutrient limitations (ammonium, nitrate, phosphate, or trace elements) and during growth cessation caused by relatively low medium pH, blue pigment production was initiated, but the pigment and its location varied.
- At pH 4.5 to 5.5, significant formation of actinorhodin occurred and was located exclusively intracellularly.
- At pH 6.0 to 7.5, a different blue pigment was produced intracellularly as well as extracellularly; it was purified and identified as gamma-actinorhodin (the lactone form of actinorhodin).
- Analysis of act mutants confirmed both pigments derive from the act biosynthetic pathway; mutants with lesions in actII-ORF2, actII-ORF3, or actVA-ORF1 (previously implicated or suggested in actinorhodin export) were impaired in gamma-actinorhodin production, suggesting synthesis of gamma-actinorhodin from actinorhodin is coupled to its export from the cell, though effects on actinorhodin production levels were also found in some mutants.
Methods
- Design: S. coelicolor A3(2) was subjected to various nutrient limitations (ammonium, nitrate, phosphate, trace elements) and to growth cessation caused by relatively low medium pH; blue pigment production, identity, and location were examined.
- The pH 6.0–7.5 pigment was purified and identified as gamma-actinorhodin; act mutants of S. coelicolor A3(2) were analyzed to test pathway origin and the role of export-related genes.
- Main analysis details beyond the abstract are not available in the provided text (only the abstract and reference list are given; the full text is a PDF link).
Limitations
- Not stated in the paper (only the abstract is available in the provided text).
- Evident from the text: the provided material is the abstract and reference list only, so experimental detail, quantitative data beyond the reported pH ranges, and any limitations discussed in the full article cannot be assessed.
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Claims the paper makes
10 Own result · 1 Own interpretation · 1 No basis given
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“However, effects on the level of actinorhodin production were also found in some mutants.”
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“but not all the”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Rests on an assumption: Streptomyces coelicolor A3(2) produces the pH indicator (red/blue) antibiotic actinorhodin.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“It was purified and identified as gamma-actinorhodin (the lactone form of actinorhodin).”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Mutants with lesions in actII-ORF2, actII-ORF3, or actVA-ORF1, previously implicated or suggested to be involved in actinorhodin export, were impaired in production of gamma-actinorhodin”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When the organism was subjected to various nutrient limitations (ammonium, nitrate, phosphate, or trace elements), and also during growth cessation caused by a relatively low medium pH, blue pigment production was initiated but the pigment and its location varied.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At pH 4.5 to 5.5, significant formation of actinorhodin occurred and was located exclusively intracellularly.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When the organism was subjected to various nutrient limitations (ammonium, nitrate, phosphate, or trace elements), and also during growth cessation caused by a relatively low medium pH, blue pigment production was initiated but the pigment and its location varied.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At pH 6.0 to 7.5 a different blue pigment was produced intracellularly as well as extracellularly.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“When the organism was subjected to various nutrient limitations (ammonium, nitrate, phosphate, or trace elements), and also during growth cessation caused by a relatively low medium pH, blue pigment production was initiated but the pigment and its location varied.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Analysis of act mutants of S. coelicolor A3(2) confirmed that both pigments are derived from the act biosynthetic pathway.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The paper relies on this without support.
Streptomyces coelicolor A3(2) produces the pH indicator (red/blue) antibiotic actinorhodin.
“The genetically well-known strain Streptomyces coelicolor A3(2) produces the pH indicator (red/blue) antibiotic actinorhodin”
The paper relies on this without support.
Mutants with lesions in actII-ORF2, actII-ORF3, or actVA-ORF1 are involved in actinorhodin export.
“Mutants with lesions in actII-ORF2, actII-ORF3, or actVA-ORF1, previously implicated or suggested to be involved in actinorhodin export”
Citations
Cites
Genetic manipulation of Streptomyces : a laboratory manual
Hopwood, D. A. (1985) · Medical Entomology and Zoology · Cited by 1,780
Self-citationCashel, M. (1996) · Medical Entomology and Zoology · Cited by 860
Malpartida, F., & Hopwood, D. A. (1984) · Nature · doi:10.1038/309462a0 · Cited by 405
Self-citationFernández‐Moreno, M. Á., Caballero, J. L., Hopwood, D. A., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90120-n · Cited by 361
Self-citationMalpartida, F., & Hopwood, D. A. (1992) · PubMed · Cited by 360
Self-citationPhosphate metabolism and cellular regulation in microorganisms
Torriani-Gorini, A. (1988) · International Journal of Biochemistry · doi:10.1016/0020-711x(88)90241-8 · Cited by 276
Dispersed growth of Streptomyces in liquid culture
Hobbs, G., Frazer, C. M., Gardner, D. J., Cullum, J., & Oliver, S. G. (1989) · Applied Microbiology and Biotechnology · doi:10.1007/bf00258408 · Cited by 276
Fernández‐Moreno, M. Á., Martínez, E., Boto, L., et al. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)41772-3 · Cited by 225
Self-citationGramajo, H. C., Takano, E., & Bibb, M. J. (1993) · Molecular Microbiology · doi:10.1111/j.1365-2958.1993.tb01174.x · Cited by 202
Genetics of Actinorhodin Biosynthesis by Streptomyces coelicolor A3(2)
Rudd, B. A. M., & HOPWOOD, D. A. (1979) · Journal of General Microbiology · doi:10.1099/00221287-114-1-35 · Cited by 198
Self-citation
Research works printed but not linked: 3
- Bergmeyer H. U. and H.-O. Beutler. 1985. Ammonia p. 454-461. In H. U. Bergmeyer J. Bergmeyer and M. Grassl (ed.) Methods of enzymatic analysis 3rd ed. vol. 8. VCH Publishers New York.
- Christiansen P. 1970. Isolierung Strukturermittlung und absolute Konfiguration neuer Actinorhodine. Ph.D. thesis. University of Göttingen Göttingen Germany.
- McNicolas C. 1991. Ph.D. thesis. University of Bristol Bristol United Kingdom.
Cited by
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Items 101–200 of 244
Can, H. J. L. V., Braake, H. A. B. T., Hellinga, C., & Luyben, K. C. A. M. (1997) · Biotechnology and Bioengineering · doi:10.1002/(sici)1097-0290(19970620)54:6 · Cited by 48
Detain, J., Rémond, C., Rodrigues, C. M., et al. (2022) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2022.100108 · Cited by 28
Role of Phosphopantetheinyl Transferase Genes in Antibiotic Production by Streptomyces coelicolor
Lu, Y., Roman, A. K. S., & Gehring, A. M. (2008) · Journal of Bacteriology · doi:10.1128/jb.00865-08 · Cited by 28
Romero-Rodríguez, A., Ruiz‐Villafán, B., Tierrafría, V. H., Rodrı́guez-Sanoja, R., & Sánchez, S. (2016) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-016-2158-9 · Cited by 27
Ji, C.-H., Kim, H., & Kang, H. (2019) · ACS Synthetic Biology · doi:10.1021/acssynbio.9b00001 · Cited by 27
Lü, J., Long, Q., Zhao, Z., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.593217 · Cited by 27
Yang, Y., Kim, T., Park, S., et al. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.00019-09 · Cited by 27
Lin, Y. B., Wang, X. Y., Fang, H., et al. (2011) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijs.0.029959-0 · Cited by 27
González-Quiñónez, N., Corte‐Rodríguez, M., García, R. Á.-F., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-40876-0 · Cited by 27
Lu, T., Cao, Q., Pang, X., et al. (2020) · Microbial Biotechnology · doi:10.1111/1751-7915.13637 · Cited by 27
Bushell, M. E., Sequeira, S. I. P., Khannapho, C., et al. (2006) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2006.06.011 · Cited by 27
Sohng, J. K. (2009) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.0803.223 · Cited by 27
Deletion of scbA enhances antibiotic production in Streptomyces lividans
Butler, M. J., Takano, E., Bruheim, P., et al. (2003) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-003-1277-8 · Cited by 27
Komatsu, M., Kuwahara, Y., Hiroishi, A., et al. (2003) · Gene · doi:10.1016/s0378-1119(03)00405-0 · Cited by 27
Umeyama, T., Tanabe, Y., Aigle, B., et al. (1996) · FEMS Microbiology Letters · doi:10.1016/0378-1097(96)00359-x · Cited by 27
Shariati, K., Ling, A. S., Fuchs, S., Dillenburger, B., Liu, W. H., & Ma, M. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202108057 · Cited by 29
Amara, A., Eriko Takano, A., & Rainer Breitling, A. (2018) · BMC Genomics · doi:10.1186/s12864-018-4905-5 · Cited by 26
Finger, M., Sentek, F., Hartmann, L., Palacio‐Barrera, A. M., Schlembach, I., Rosenbaum, M. A., & Büchs, J. (2022) · Engineering in Life Sciences · doi:10.1002/elsc.202100151 · Cited by 25
Reciprocal Regulation between SigK and Differentiation Programs inStreptomyces coelicolor
Mao, X., Zhou, Z. M., Hou, X., Guan, W., & Li, Y. (2009) · Journal of Bacteriology · doi:10.1128/jb.00875-09 · Cited by 25
Feng, W., Mao, X., Liu, Z.-H., et al. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3619-2 · Cited by 24
Sakr, A. A., Ghaly, M. F., Edwards, H. G. M., et al. (2020) · Geomicrobiology Journal · doi:10.1080/01490451.2020.1754533 · Cited by 24
Palanichamy, V., Hundet, A., Mitra, B., et al. (2011) · International Journal of Plant Animal and Environmental Sciences · Cited by 23
Jin, X.-M., Chang, Y., Lee, J. H., et al. (2017) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1707.07046 · Cited by 23
Holtmann, D., Vernen, F., Müller, J., et al. (2016) · Sustainable Chemistry and Pharmacy · doi:10.1016/j.scp.2016.09.001 · Cited by 22
Neumeyer, M., & Brückner, R. (2017) · Angewandte Chemie International Edition · doi:10.1002/anie.201611183 · Cited by 22
Programmable polyketide biosynthesis platform for production of aromatic compounds in yeast
Jakočiūnas, T., Klitgaard, A., Kontou, E. E., et al. (2020) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2020.01.004 · Cited by 22
Directed Transfer of Large DNA Fragments between Streptomyces Species
Hu, Z., Hopwood, D. A., & Khosla, C. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.5.2274-2277.2000 · Cited by 22
Self-citationWang, X., Fu, Y., Wang, M., et al. (2021) · ACS Synthetic Biology · doi:10.1021/acssynbio.1c00152 · Cited by 21
Yang, Y.-H., Song, E., Kim, J.-N., et al. (2012) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3803-4 · Cited by 21
Chen, W., & Qin, Z. (2011) · BMC Microbiology · doi:10.1186/1471-2180-11-243 · Cited by 21
Nass, N. M., Farooque, S., Hind, C. K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-17232-1 · Cited by 21
Jovetic, S., Feroggio, M., Marinelli, F., et al. (2008) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-008-0392-z · Cited by 21
Kanth, B. K., Jnawali, H. N., Niraula, N. P., et al. (2010) · Microbiological Research · doi:10.1016/j.micres.2010.07.003 · Cited by 21
Lewis, R. A., Shahi, S. K., Laing, E., et al. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-78 · Cited by 20
“45 μm predried, preweighed nitrocellulose membranes (Millipore, Watford, UK) and the culture filtrate was retained for actinorhodin assay [21] and nutrient analyses (PO4 , NH4 + and Glucose) using a Merck RQFlex10TM reflectometer.”
MethodDiscovery of a Cryptic Intermediate in Late Steps of Mithramycin Biosynthesis
Wheeler, R., Yu, X., Hou, C., et al. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201910241 · Cited by 20
Yonekawa, T., Ohnishi, Y., & Horinouchi, S. (1999) · Microbiology · doi:10.1099/00221287-145-9-2273 · Cited by 20
Pleiotropic effect of a null mutation in the cvn1 conservon of Streptomyces coelicolor A3(2)
Takano, H., Hashimoto, K., Yamamoto, Y., et al. (2011) · Gene · doi:10.1016/j.gene.2011.01.005 · Cited by 19
Nguyen, L., Kalachová, L., Novotná, J., Holub, M., Kofroňová, O., Benada, O., Thompson, C. J., & Weiser, J. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.6.2848-2852.2005 · Cited by 19
Allantoin catabolism influences the production of antibiotics in Streptomyces coelicolor
Navone, L., Casati, P., Licona‐Cassani, C., Marcellin, E., Nielsen, L. K., Rodrı́guez, E., & Gramajo, H. C. (2013) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-013-5372-1 · Cited by 18
Aiswarya, G., Vijayanathan, M., Sreekumar, S., Jasim, B., Menon, T. G., Radhakrishnan, E. K., & Soniya, E. V. (2021) · Current Molecular Pharmacology · doi:10.2174/1874467214666210319145816 · Cited by 18
Galet, J., Deveau, A., Hôtel, L., et al. (2014) · Archives of Microbiology · doi:10.1007/s00203-014-1000-4 · Cited by 17
Lewis, R. A., Wahab, A., Bucca, G., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0200673 · Cited by 17
A facile Garratt–Braverman cyclization route to intercalative DNA-binding bis-quinones
Addy, P. S., Dutta, S., Biradha, K., et al. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.10.030 · Cited by 16
Kronheim, S., Solomon, E., Ho, L., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-36938-z · Cited by 16
Zhang, Y., Wang, L., Zhang, S., et al. (2008) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2008.01070.x · Cited by 16
Yi, J. S., Kim, M., Kim, S.-J., et al. (2015) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1409.09009 · Cited by 16
Effects of phosphate limitation on agarase production byStreptomyces lividansTK21
Parro, V., Mellado, R. P., & Harwood, C. R. (1998) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1998.tb12808.x · Cited by 16
Rajesh, T., Song, E., Kim, J., et al. (2011) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-011-3581-z · Cited by 15
Ostash, B., Doud, E. H., & Walker, S. (2012) · Archives of Microbiology · doi:10.1007/s00203-012-0827-9 · Cited by 15
López-García, M. T., Yagüe, P., González-Quiñónez, N., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00312 · Cited by 15
Lim, Y., Jung, E. S., Lee, J. H., Kim, E. J., Hong, S. J., Lee, Y. H., & Lee, C. H. (2018) · PLoS ONE · doi:10.1371/journal.pone.0207541 · Cited by 15
Takano, H., Hagiwara, K., & Uéda, K. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6325-z · Cited by 15
Nakano, T., Miyake, K., Ikeda, M., et al. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.4.1400-1404.2000 · Cited by 15
Recombinatorial biosynthesis of polyketides
Starčević, A., Wolf, K., Diminić, J., et al. (2011) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-011-1049-x · Cited by 14
Yang, Y., Song, E., Lee, B.-R., et al. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.02617-09 · Cited by 14
Prodiginines Postpone the Onset of Sporulation in Streptomyces coelicolor
Tenconi, E., Traxler, M. F., Tellatin, D., van Wezel, G. P., & Rigali, S. (2020) · Antibiotics · doi:10.3390/antibiotics9120847 · Cited by 14
TOF-SIMS investigation of Streptomyces coelicolor, a mycelial bacterium
Vaidyanathan, S., Fletcher, J. S., Lockyer, N. P., et al. (2008) · Applied Surface Science · doi:10.1016/j.apsusc.2008.05.134 · Cited by 14
Anderson, T. B., Brian, P., Riggle, P. J., et al. (1999) · Microbiology · doi:10.1099/00221287-145-9-2343 · Cited by 14
AllR Controls the Expression of Streptomyces coelicolor Allantoin Pathway Genes
Navone, L., Macagno, J. P., Licona‐Cassani, C., Marcellin, E., Nielsen, L. K., Gramajo, H. C., & Rodrı́guez, E. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.02098-15 · Cited by 13
López-García, M. T., Rioseras, B., Yagüe, P., et al. (2014) · PubMed · doi:10.2436/20.1501.01.209 · Cited by 13
Klumbys, E., Xu, W., Koduru, L., et al. (2024) · Microbial Cell Factories · doi:10.1186/s12934-024-02416-y · Cited by 12
“The parental strain is known for being a prolific producer of the pigmented antibiotic actinorhodin, and the derivative strain is equally prolific when the actinorhodin gene cluster in re-introduced [26, 57], while the closely related S. lividans strain demonstrates only moderate yields.”
BackgroundTunable population dynamics in a synthetic filamentous coculture
Finger, M., Palacio‐Barrera, A. M., Richter, P., et al. (2022) · MicrobiologyOpen · doi:10.1002/mbo3.1324 · Cited by 11
Actinomycins from Soil-Inhabiting Streptomyces as Sources of Antibacterial Pigments for Silk Dyeing
Nuanjohn, T., Suphrom, N., Nakaew, N., et al. (2023) · Molecules · doi:10.3390/molecules28165949 · Cited by 11
Jain, M., Chow, E. D., & Cox, J. S. (2014) · ASM Press eBooks · doi:10.1128/9781555815783.ch12 · Cited by 11
Micro-segmented flow and multisensor-technology for microbial activity profiling
Kürsten, D., Kothe, E., Wetzel, K., et al. (2014) · Environmental Science Processes & Impacts · doi:10.1039/c4em00255e · Cited by 11
García-Cancela, P., González-Quiñónez, N., Corte‐Rodríguez, M., et al. (2022) · Metallomics · doi:10.1093/mtomcs/mfac015 · Cited by 11
Tierrafría, V. H., Licona‐Cassani, C., Maldonado-Carmona, N., et al. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7811-2 · Cited by 10
Besaury, L., Floret, J., & Rémond, C. (2021) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/ijsem.0.004963 · Cited by 10
“Digital DNA–DNA relatedness (dDDR) values were calculated using the genome- to-genome distance calculation [21] method between strain arapr2 T and the closely related strains.”
Extracellular Carbohydrate Metabolites from Streptomyces coelicolor A3(2)
Pospíšil, S., Sedmera, P., Halada, P., et al. (2007) · Journal of Natural Products · doi:10.1021/np0606188 · Cited by 10
de Orduña, R. M. (2000) · Journal of Biotechnology · doi:10.1016/s0168-1656(99)00215-1 · Cited by 10
Loss of phosphomannomutase activity enhances actinorhodin production in Streptomyces coelicolor
Yang, Y., Song, E., Park, S.-H., et al. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2368-y · Cited by 9
“After centrifugation in a micro-centrifuge for 10 min, 900 μL of the supernatant was sampled for further analysis according to previously reported procedures ( Bystrykh et al. 1996 ).”
MethodJager, D. D., Sheldon, M. S., & Edwards, W. (2009) · Enzyme and Microbial Technology · doi:10.1016/j.enzmictec.2009.08.010 · Cited by 9
Song, E., Rajesh, T., Lee, B.-R., et al. (2013) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-013-4847-4 · Cited by 9
Neumeyer, M., & Brückner, R. (2017) · Angewandte Chemie · doi:10.1002/ange.201611183 · Cited by 9
Nováková, R., Homerová, D., Csolleiova, D., et al. (2022) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-022-12187-4 · Cited by 8
Lü, L., Cui, H., Chen, Y. N., et al. (2002) · Folia Microbiologica · doi:10.1007/bf02818787 · Cited by 8
Govindarajan, G., Santhi, V. S., & Solomon, R. D. J. (2017) · Archives of Biological Sciences · doi:10.2298/abs170224019g · Cited by 8
Jeon, J.-M., Choi, T., Lee, B.-R., et al. (2019) · Biotechnology and Bioprocess Engineering · doi:10.1007/s12257-019-0084-8 · Cited by 8
Metabolomics Reveals a “Trimeric” γ‐Actinorhodin from Streptomyces coelicolor M145
Marshall, A. P., & Carlson, E. E. (2023) · ChemBioChem · doi:10.1002/cbic.202200757 · Cited by 7
Forero, A. V. F., Sánchez, M., Chávez, A., et al. (2012) · Canadian Journal of Microbiology · doi:10.1139/w2012-100 · Cited by 7
Yagüe, P., Willemse, J., Xiao, X.-S., Zhang, L., Manteca, Á., & van Wezel, G. V. (2022) · Antonie van Leeuwenhoek · doi:10.1007/s10482-022-01778-w · Cited by 6
González-Quiñónez, N., Gutiérrez‐del‐Río, I., García-Cancela, P., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221810143 · Cited by 7
Deletion of TerD-domain-encoding genes: effect on Streptomyces coelicolor development
Sanssouci, É., Lerat, S., Daigle, F., Grondin, G., Shareck, F., & Beaulieu, C. (2012) · Canadian Journal of Microbiology · doi:10.1139/w2012-101 · Cited by 7
Arabolaza, A. L., Banchio, C., & Gramajo, H. C. (2006) · Microbiology · doi:10.1099/mic.0.28553-0 · Cited by 7
Development of a versatile chassis for the efficient production of diverse type II polyketides
Zou, Y., Wang, R., Liu, Z., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62659-0 · Cited by 6
“This plasmid harbors the complete native ACT BGC, which was successfully heterologously expressed 49 (Fig.”
InfluentialBiosynthesis of Indigoidine in Microorganisms: Strategies and Applications
Zhao, X., Leng, X., & Luo, Y. (2026) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00800 · Cited by 6
Vignesh, S., Anandu, P. M., Varrier, G. S. G., et al. (2024) · Indian Journal of Microbiology · doi:10.1007/s12088-024-01323-5 · Cited by 6
Fernández-García, G., García-Cancela, P., Corte‐Rodríguez, M., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-07164-8 · Cited by 6
“Undecylprodigiosin and actinorhodin were spectrophotometrically quan-ti fi ed via the methodology developed by Tsao et al. 65 and Bystrykh et al. 66 .”
Kumar, K., & Bruheim, P. (2022) · 3 Biotech · doi:10.1007/s13205-022-03146-x · Cited by 5
A tunable and reversible thermo-inducible bio-switch for streptomycetes
Lv, L., Liu, S., Fu, Y., Zhang, Y., Wang, M., Sun, J., Wang, Y., Lü, Y., & Niu, G. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae1236 · Cited by 5
“The quantification of actinorhodin was performed essentially as described previously ( 23 ).”
Rajesh, T., Jeon, J.-M., Song, E., et al. (2013) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-013-0635-y · Cited by 5
El-Nasser, N. H. A., Helmy, S. M., Ali, A. M. M., et al. (2010) · Cited by 5
Liu, S., Xiao, F., Lv, L., Wang, M., Li, W., & Niu, G. (2025) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2025.05.010 · Cited by 4
“Actinorhodin quantification was then carried out by measuring the absorbance at 640 nm [35].”
Astudillo, Á., Hormazábal, E., Quiróz, A., et al. (2024) · Chemical and Biological Technologies in Agriculture · doi:10.1186/s40538-024-00612-x · Cited by 4
“Variations in cultivation parameters such as initial pH or nutrient content can significantly modulate not only growth kinetics but also enzymatic profiles of Streptomyces spp., consequently influencing the synthesis and yield of pigments during the fermentation process [23, 44].”
BackgroundTranslational Value of Natural Pigments with Reference to Healthcare and Cosmetic Applications
Saravanan, T. S., Gopikrishnan, V., Manikkam, R., Kaari, M., Annamalai, K. K., Song, J., & Soytong, K. (2024) · Springer eBooks · doi:10.1007/978-981-97-1777-4_16 · Cited by 4
Kim, Y. J. (2011) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1105.05003 · Cited by 4
Fernández-García, G., González-Quiñónez, N., Rioseras, B., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094984 · Cited by 4
Editing Streptomyces genome using target AID system fused with UGI‐degradation tag
Apriliana, P., Kahar, P., Kashiwagi, N., Kondo, A., & Ogino, C. (2024) · Engineering in Life Sciences · doi:10.1002/elsc.202400005 · Cited by 3
The oxidative rearrangements in bacterial aromatic polyketide biosynthesis
Jiao, F., Li, S., Qiao, H., et al. (2025) · Natural Product Reports · doi:10.1039/d5np00049a · Cited by 3
Song, J. Y. (2013) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1207.07030 · Cited by 3
Metadata
- Authors
- Bystrykh, L. V., Fernández-Moreno, M. A., Herrema, J. K., Malpartida, F., Hopwood, D. A., & Dijkhuizen, L.
- Affiliations
- University of Groningen (NL)
- Department of Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, The Netherlands.
- Venue
- Journal of Bacteriology
- Publisher
- American Society for Microbiology
- Published
- 1996-04
- Volume
- 178
- Issue
- 8
- Pages
- 2238-2244
- ISSN
- 0021-9193 (ISSN-L)
- 1098-5530
- PMC
- PMC177931
- OpenAlex
- W2142314320
- Cited by
- 245
- References
- 42
- Citations by year
- 2026: 9 · 2025: 5 · 2024: 10 · 2023: 7 · 2022: 10 · 2021: 7 · 2020: 11 · 2019: 11 · 2018: 7 · 2017: 9 · 2016: 9 · 2015: 9 · 2014: 11 · 2013: 12 · 2012: 10
- FWCI
- 4.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Bacteriology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (submittedVersion)
- PubMed Central (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
- Default journal
- Topics
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Microbial Metabolism and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- actinorhodin, Streptomyces coelicolor A3(2), blue pigments, acid-base indicators, lactone formation, nutrient limitation, low pH, intracellular pigments
- MeSH terms
- Benzoisochromanequinones, Anthraquinones, Anti-Bacterial Agents, Biological Transport, Hydrogen-Ion Concentration, Lactones, Mutation, Pigments, Biological, Spectrophotometry, Streptomyces
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