The DOI matches its Crossref record; 41 of the 42 references it cites were found in a registry or an index.
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.
Overview
AI snapshot
Written from the paper’s full text.
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.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
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
Sorted by citations
Items 201–244 of 244
Lubbers, M., van Wezel, G. P., & Claessen, D. (2022) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2022.106660 · Cited by 3
Lu, T., Wang, Q., Cao, Q., Xia, Y., Xun, L., & Liu, H. (2023) · Antioxidants · doi:10.3390/antiox12020312 · Cited by 3
Discovery of a Cryptic Intermediate in Late Steps of Mithramycin Biosynthesis
Wheeler, R., Yu, X., Hou, C., et al. (2019) · Angewandte Chemie · doi:10.1002/ange.201910241 · Cited by 3
The Use of Streptomyces coelicolor in the Removal of Heavy Metals
Öztürk, A. (2015) · Advanced Techniques in Biology & Medicine · doi:10.4172/2379-1764.1000168 · Cited by 3
Increased Vulnerability to Physical Stress by Inactivation of NdgR in Streptomyces coelicolor
Lee, B.-R., Yi, D.-H., Song, E., et al. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-015-1536-z · Cited by 2
Velho-Pereira, S., & Kamat, N. M. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/060392 · Cited by 2
Versatile polyketide biosynthesis platform for production of aromatic compounds in yeastPreprint
Jakočiūnas, T., Klitgaard, A., Romero-Suárez, D., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/618751 · Cited by 2
Silica gel-mediated chemical degradation of dimeric pyranonaphthoquinones into their monomeric units
Ozakai, C., Kitamura, K., & Kaku, H. (2023) · New Journal of Chemistry · doi:10.1039/d3nj01957h · Cited by 1
Regulación del metabolismo en Streptomyces: Control por ArgR
Muñoz, A. M. B. (2014) · doi:10.18002/10612/3273 · Cited by 1
Cattini, N. (2007) · Surrey Research Insight Open Access (The University of Surrey) · Cited by 1
Sunaryanto, R., & Mahsunah, A. H. (2015) · SQUALEN Bulletin of Marine and Fisheries Postharvest and Biotechnology · doi:10.15578/squalen.v10i1.101
ATIMICROBIAL ACTIVITY AD CYTOTOXICITY TESTIG OF BLUE PIGMET BY STREPTOMYCETES SPECIES
Usha, R., MALA, K. K., & PALANISWAMY, M. (2010)
Analysis of Multivariate Sensor Data for Monitoring of
Rnnest, N. P. (2010)
Specific and global networks of gene regulation in Streptomyces coelicolor
Hasan, A. H. (2015) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
Gorzelnik, K. V. (2014) · OakTrust (Texas A&M University Libraries)
Mechanisms of resistance to β-lactam antibiotics in Streptomycetes
Alkut, W. (2016) · Liverpool John Moores University · doi:10.24377/ljmu.t.00004613
Manipulating posttranslational modification in natural product biosynthesis
Foley, T. L. (2010) · eScholarship (California Digital Library)
MtrAB-LpqB : a conserved pathway regulating cell division in the phylum Actinobacteria?
Som, N. F. (2016) · UEA Digital Repository (University of East Anglia)
Regulation and Function of Redox Sensor SoxR in Streptomyces coelicolor
싱아툴쿠마르 (2014) · Seoul National University Open Repository (Seoul National University)
The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor
Mak, S. (2017) · TSpace (University of Toronto)
이정상 (2018) · Seoul National University Open Repository (Seoul National University)
Velho-Pereira, S. (2016) · SSRN Electronic Journal · doi:10.2139/ssrn.2986073
INTERACTIONS OF POST-PKS ENZYMES OF THE MITHRAMYCIN BIOSYNTHETIC PATHWAY
Wheeler, R. (2021) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2021.043
Ahmad, W. A., Ahmad, W. Y. W., Zakaria, Z. A., et al. (2011) · Springer briefs in molecular science · doi:10.1007/978-3-642-24520-6_1
de Oliveira, R. V. F. (2023) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2023.tde-19092023-153712
A tunable and reversible thermo-inducible bio-switch for streptomycetesPreprint
Niu, G., Lv, L., Fu, Y., et al. (2024) · Research Square · doi:10.21203/rs.3.rs-4838944/v1
Klumbys, E., Xu, W., Koduru, L., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26725490
Nag, A., Kumbhar, C., & Mehra, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.22.695978
Astudillo, Á., Hormazábal, E., Diez, M. C., Rubilar, O., de Alencar, S. M., Scheuermann, E. S. S., Briceño, G. E., & Heidi Schalchli, S. (2025) · Chemical and Biological Technologies in Agriculture · doi:10.1186/s40538-025-00907-7
“In line with these findings, under optimized cultivation conditions, the chemical properties of the blue pigment, particularly its acid/base indicator behavior and maximum absorption wavelength at 640 nm [26], suggest the presence of actinorhodin and/or actinorhodin-related compounds.”
InfluentialNag, A., Kumbhar, C., & Mehra, S. (2026) · Research Square · doi:10.21203/rs.3.rs-8963257/v1
Mehmood, N. (2011) · theses.fr (ABES) · doi:10.70675/ccb01771za539z4058z970czb7e371e9b3e1
“5 undecylprodigiosin was produced instead of actinorhodin (Bystrykh et al., 1996).”
InfluentialStructural Organization and Antimicrobial Properties of Streptomyces sp. Lzd4kr
Носков, А. Е., Поливцева, В. Н., Machulin, A. V., et al. (2026) · Microbiology · doi:10.1134/s0026261725604956
“Acti-norhodin, originally described in Streptomyces coeli-color A3(2) (Bystrykh et al., 1996), is an aromatic polyketide produced by type II polyketide synthases (T2PKS) and one of the best studied blue streptomy-cete antibiotics.”
Nitroflavone Derivatives Inhibit the Production of Actinorhodin in Streptomyces coelicolor
Slimene, S., David, M., Dauzonne, D., et al. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48070744
“This study uses the extensively researched model strain SC M145, which produces large quantities of ACT [5,32].”
Plant-associated Streptomyces detoxify the mycotoxin fusaric acid by amino acid conjugationPreprint
Diab, E., Du, C., Verdel, S. C., Kunnen, M. R., Stuij, R., Elsayed, S. S., Raaijmakers, J. M., & van Wezel, G. P. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.26.747244
Chen, C., Zhao, B., Zhu, Q., Wang, X., Ji, N., & Zhu, Y. (2026) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-026-05269-2
“Secondly, granaticin exhibits pronounced pH-dependent color changes (red under acidic conditions and purple–blue under alkaline conditions), indicating its potential as a responsive pigment rather than merely a conventional colo-rant (Bystrykh et al. 1996).”
High-Throughput Media Screening for Modulation of Secondary Metabolite Production in Actinomycetes
Khan, M. A. R., Rajwani, R., Haro, J., & Bewley, C. A. (2026) · Journal of Natural Products · doi:10.1021/acs.jnatprod.6c00723
Chen, Y., Dou, K., Lv, L., Wang, M., & Niu, G. (2026) · ACS Synthetic Biology · doi:10.1021/acssynbio.6c00563
Illuminating Streptomyces : Raman Spectroscopy for Antibiotic Detection and Monitoring
Mikulová, A., Bobek, J., Kizovský, M., et al. (2026) · Journal of Raman Spectroscopy · doi:10.1002/jrs.70217
Sun, F., Zhao, S., Wang, S., et al. (2013) · Lecture notes in electrical engineering · doi:10.1007/978-3-642-37916-1_44
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-13, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-13 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review