![]() Galanopoulou AP, Moraїs S, Georgoulis A, Morag E, Bayer EA, Hatzinikolaou DG (2016) Insights into the functionality and stability of designer cellulosomes at elevated temperatures. įlassig RJ, Fachet M, Hoffner K, Barton PI, Sundmacher K (2016) Dynamic flux balance modeling to increase the production of high-value compounds in green microalgae. įeng G, Zhu M, Liu L, Li C (2019) A quantitative one-pot synthesis method for industrial azo pigments with recyclable wastewater. Appl Environ Microb 78(14):4771–4780ĭueber JE, Wu GC, Malmirchegini GR, Moon TS, Petzold CJ, Ullal AV, Prather KL, Keasling JD (2009) Synthetic protein scaffolds provide modular control over metabolic flux. J Biotechnol 157(1):96–99Ĭude WN, Mooney J, Tavanaei AA, Hadden MK, Frank AM, Gulvik CA, May AL, Buchan A (2012) Production of the antimicrobial secondary metabolite indigoidine contributes to competitive surface colonization by the marine roseobacter Phaeobacter sp. The yield and titer of indigoidine was improved by arranging the pathway enzymes.īrachmann AO, Kirchner F, Kegler C, Kinski SC, Schmitt I, Bode HB (2012) Triggering the production of the cryptic blue pigment indigoidine from Photorhabdus luminescens.The inhibition caused by excess Gln was relieved by proper designed scaffold.The scaffold system improved supplement of Gln for indigoidine production from Glu.Protein scaffold systems were designed to arrange the indigoidine synthetic pathway.The optimization strategies by protein scaffold should be applicative to other pathways with complex substrate demands. To our knowledge, this was the most efficient indigoidine productivity achieved so far. The batch fermentation with the optimum strain in a 5-L reactor achieved an indigoidine titer of 14 g/L in 60 h. The titer is 5 g/L higher than the control without Glu supplemented (6.9 g/L), meaning that 97% of the supplemented Glu was transformed into indigoidine. The highest titer of indigoidine was 12 g/L, which was two folds of the control without scaffold (5.8 g/L). ![]() The optimum Glu concentration (6 g/L) for the strain was higher than those of the strains recruiting Sc-IndC on the GBD domain, which was away from the PDZ domain recruiting GlnA. In the strain, the GlnA supplied sufficient local Gln for Sc-IndC from Glu, and the generated Gln was immediately consumed by Sc-IndC to relieve cell growth inhibition caused by Gln. ![]() The strain recruiting GlnA, Sc-IndC, and IndB on the PDZ, SH3, and GBD domains of scaffold P1S2G1, respectively, was the most efficient. #PROTEIN SCAFFOLD PDF SERIES#We identified the Streptomyces chromofuscus ATCC 49982 derived IndC (Sc-IndC) as an more efficient IndC compared to other IndCs applied for constructing indigoidine-producting strains, and designed series of protein scaffold complexes with architectures of PDZ, SH3, and GBD domains (PxSyG1) to arrange the pathway enzymes. ![]() Supplementing Glu instead of Gln may improve the productive and economic efficiency of indigoidine, but the local activities and positions of the indigoidine pathway enzymes GlnA, Sc-IndC, and the helper protein of Sc-IndC (IndB) should be well arranged. But, Gln is expensive, and excess Gln inhibits indigoidine production of the recombinant strain. Indigoidine production can be improved by enhancing Gln pool via supplementing Gln directly or converting metabolism glutamate (Glu) to Gln by glutamine synthetase (GlnA). Indigoidine is a dark-blue natural pigment with application prospect and synthesized from glutamine (Gln) by series of indigoidine synthetases (IndCs). ![]()
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