Pregled bibliografske jedinice broj: 491058
Evolutionary dynamics of modular polyketide synthases with implications for protein design and engineering
Evolutionary dynamics of modular polyketide synthases with implications for protein design and engineering // Journal of antibiotics, 64 (2011), 1; 89-92 doi:10.1038/ja.2010.141 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 491058 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Evolutionary dynamics of modular polyketide synthases with implications for protein design and engineering
Autori
Žučko, Jurica ; Cullum, John ; Hranueli, Daslav ; Long, Paul F.
Izvornik
Journal of antibiotics (0021-8820) 64
(2011), 1;
89-92
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
antibiotic; evolution; synonymous substitution; non-synonymous substitution; (a)/ (s) ratio; K(a)K(s) ratio; polyketide; Streptomyces
Sažetak
Attempts at generating novel chemistries by genetically manipulating polyketide synthases (PKSs) usually result in no detectable or poor product yield. Understanding processes that drive the evolution of PKSs might provide a solution to this problem. The synonymous-to-non-synonymous nucleotide substitution ratios across alignments of well characterized PKS modules were examined using a sliding windows approach. Not surprisingly, the overall substitution ratios showed that PKS modules are generally under strong purifying selection, confirming experimental observations that changes to the primary amino acid sequence, regardless of whether these changes are conservative or not, will most likely result in some loss in function. Despite the masking effect of negative selection, by judicious choice of window size, it was possible to recognise amino acid residues that appear to be under strong positive selection. The importance of these amino acids has not been recognised by other analysis methods before and we suggest that they may function to “fine tune” modular PKSs. Future efforts will concentrate on understanding if this “fine tuning” is at the level of protein expression, for example, transcription or translation, or at the level of protein function, for example, efficient selection and channelling of acyl intermediates between domains.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija
POVEZANOST RADA
Projekti:
058-0000000-3475 - Generiranje potencijalnih lijekova u uvjetima in silico (Hranueli/Jurica Žučko, Daslav, MZOS ) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE