Rhodotorula mucilaginosa, a carotenoid producing yeast strain from a Patagonian high-altitude lake
Language English Country United States Media print
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
15143736
DOI
10.1007/bf02931640
Knihovny.cz E-resources
- MeSH
- Antibiosis MeSH
- Basidiomycota growth & development MeSH
- Pigments, Biological biosynthesis MeSH
- Biomass MeSH
- DNA Fingerprinting MeSH
- DNA, Fungal analysis isolation & purification MeSH
- Nitrogen metabolism MeSH
- Glucose metabolism MeSH
- Carotenoids biosynthesis MeSH
- Water Microbiology * MeSH
- Microsatellite Repeats genetics MeSH
- Mycological Typing Techniques MeSH
- Polymerase Chain Reaction MeSH
- Rhodotorula classification isolation & purification metabolism physiology MeSH
- Fresh Water microbiology MeSH
- Carbon metabolism MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Geographicals
- Argentina MeSH
- Names of Substances
- Pigments, Biological MeSH
- DNA, Fungal MeSH
- Nitrogen MeSH
- Glucose MeSH
- Carotenoids MeSH
- Carbon MeSH
The red yeast Rhodotorula mucilaginosa strain CRUB 0138 (previously identified as R. lactosa) was isolated from a high-altitude Patagonian Lake Toncek (1700 m a.s.l.), and assigned with mucilaginosa species. Its biochemical, physiological and molecular features were assessed and compared to R. mucilaginosa PYCC 5166 type strain using a polyphasic approach; in addition, biomass and carotenoid pigment production at different C/N ratios were determined in an incubator shaker. Phenetic characterization by means of 70 current physiological tests including assimilation of aldaric acids and aromatic compounds, and also the ability to grow with amino acids as sole carbon sources, was carried out. According to numerical taxonomy calculations, similarity indexes between R. mucilaginosa CRUB 0138 and PYCC 5166 type strain were 0.86 and 0.77, corresponding to a complete set of physiological tests and MSP-PCR (Mini/Micro Satellite Primed PCR; (GTG)5, M13 and (GAC)5 primers were employed) fingerprinting. Killer activity against 2 native strains, Rhodosporidium kratochvilovae and R. mucilaginosa was detected. Maximum biomass-glucose conversion efficiency (87%) and maximum carotenoid yield (2.32 mg/L) were obtained at C/N = 5 in culture medium containing 10 and 40 g/L glucose, respectively. Different C/N ratios did not influence carotenoid pigment production but low C/N enhanced biomass yield.
See more in PubMed
Arch Microbiol. 1995 Sep;164(3):173-9 PubMed
Folia Microbiol (Praha). 2002;47(3):241-5 PubMed
Folia Microbiol (Praha). 2001;46(5):397-401 PubMed
Appl Environ Microbiol. 1997 Nov;63(11):4471-8 PubMed
Int J Syst Evol Microbiol. 2001 Mar;51(Pt 2):687-97 PubMed
Can J Microbiol. 1999 Jun;45(6):491-512 PubMed
Antonie Van Leeuwenhoek. 2003;84(3):217-27 PubMed
J Bacteriol. 1964 Dec;88:1688-94 PubMed
Antonie Van Leeuwenhoek. 2003;84(4):313-22 PubMed
Folia Microbiol (Praha). 2001;46(5):402-6 PubMed
Folia Microbiol (Praha). 2002;47(1):56-60 PubMed
Appl Microbiol Biotechnol. 2001 Apr;55(3):341-7 PubMed
J Clin Microbiol. 1993 Sep;31(9):2274-80 PubMed
FEMS Yeast Res. 2002 Mar;2(1):47-58 PubMed
Microbiol Rev. 1996 Jun;60(2):407-38 PubMed
Biotechnol Bioeng. 1994 Oct;44(8):888-94 PubMed
Can J Microbiol. 1992 Dec;38(12 ):1242-51 PubMed