[1. Khosravi-Darani K., Bucci DZ. Application of poly(hydroxyalkanoate) in food packaging: Improvements by nanotechnology. Chem Biochem Eng Q 2015; 29(2): 275-285.10.15255/CABEQ.2014.2260]Search in Google Scholar
[2. Nigmatullin R, Thomas P, Lukasiewicz B, Puthussery H, Roy I. Polyhydroxyalkanoates, a family of natural polymers, and their applications in drug delivery. J Chem Technol Biotechnol 2015; 90(7): 1209-1221. 10.1002/jctb.4685]Search in Google Scholar
[3. Koller M. Poly(hydroxyalkanoates) for food packaging: Application and attempts towards implementation. Appl Food Biotechnol 2014; 1(1): 3-15.]Search in Google Scholar
[4. Ong SY, Sudesh K. Effects of polyhydroxyalkanoate degradation on soil microbial community. Polym Degrad Stab 2016; 131: 9-19.10.1016/j.polymdegradstab.2016.06.024]Search in Google Scholar
[5. Berezina N, Yada B, Lefebvre R. From organic pollutants to bioplastics: insights into the bioremediation of aromatic compounds by Cupriavidus necator. New Biotechnol 2015; 32(1): 47-53.10.1016/j.nbt.2014.09.003]Search in Google Scholar
[6. Jendrossek D, Pfeiffer D. New insights in the formation of polyhydroxyalkanoate granules (carbonosomes) and novel functions of poly(3‐hydroxybutyrate). Environ Microbiol 2014; 16(8): 2357-2373.10.1111/1462-2920.12356]Search in Google Scholar
[7. Masood F, Yasin T, Hameed A. Polyhydroxyalkanoates-what are the uses? Current challenges and perspectives. Crit Rev Biotechnol 2015; 35(4): 514-521.10.3109/07388551.2014.913548]Search in Google Scholar
[8. Obruca S, Sedlacek P, Mravec F, Samek O, Marova, I. Evaluation of 3-hydroxybutyrate as an enzyme-protective agent against heating and oxidative damage and its potential role in stress response of poly(3-hydroxybutyrate) accumulating cells. Appl Microbiol Biotechnol 2016; 100(3): 1365-1376.10.1007/s00253-015-7162-4]Search in Google Scholar
[9. Reddy CSK, Ghai R, Kalia V. Polyhydroxyalkanoates: an overview. Biores Technol 2003; 87(2): 137-146.10.1016/S0960-8524(02)00212-2]Search in Google Scholar
[10. Steinbuchel A. Perspectives for biotechnological production and utilization of biopolymers: metabolic engineering of polyhydroxyalkanoate biosynthesis pathways as a successful example. Macromol Biosci 2001; 1(1): 1-24.10.1002/1616-5195(200101)1:1<1::AID-MABI1>3.0.CO;2-B]Search in Google Scholar
[11. Keshavarz T, Roy I. Polyhydroxyalkanoates: bioplastics with a green agenda. Curr Opin Microbiol 2010; 13(3): 321-326.10.1016/j.mib.2010.02.006]Open DOISearch in Google Scholar
[12. Chen GQ, Hajnal I. The ‘PHAome’. Trends Biotechnol 2015; 33(10): 559-564.]Search in Google Scholar
[13. Koller M, Maršalek L, Miranda de Sousa Dias M, Braunegg G. Producing microbial polyhydroxyalkanoate (PHA) biopolyesters in a sustainable manner. New Biotechnol 2017; 37(A): 24-38.10.1016/j.nbt.2016.05.001]Open DOISearch in Google Scholar
[14. Narodoslawsky M, Shazad K, Kollmann R, Schnitzer H. LCA of PHA Production-Identifying the Ecological Potential of Bio-plastic. Chem Biochem Eng Q 2015; 29(2): 299-305.10.15255/CABEQ.2014.2262]Search in Google Scholar
[15. Novak M, Koller M, Braunegg M, Horvat P. Mathematical modelling as a tool for optimized PHA production. Chem Biochem Eng Q 2015; 29(2): 183-220.10.15255/CABEQ.2014.2101]Search in Google Scholar
[16. Kaur G, Roy I. Strategies for large-scale production of polyhydroxyalkanoates. Chem Biochem Eng Q 2015; 29(2): 157-172. 10.15255/CABEQ.2014.2255]Search in Google Scholar
[17. Haas C, El-Najjar T, Virgolini N, Smerilli M, Neureiter M. High cell-density production of poly (3-hydroxybutyrate) in a membrane bioreactor. New Biotechnol 2017; 37(A): 117-122.10.1016/j.nbt.2016.06.1461]Search in Google Scholar
[18. Luo HP, Kemoun A, Al-Dahhan MH, Sevilla JF, Sanchez JG, Camacho FG, Grima EM. Analysis of photobioreactors for culturing high-value microalgae and cyanobacteria via an advanced diagnostic technique: CARPT. Chem Eng Sci 2003; 58(12): 2519-2527.10.1016/S0009-2509(03)00098-8]Search in Google Scholar
[19. Dionisi D, Majone M, Vallini G, Di Gregorio S, Beccari M. Effect of the applied organic load rate on biodegradable polymer production by mixed microbial cultures in a sequencing batch reactor. Biotechnol Bioeng 2006; 93(1): 76-88.10.1002/bit.2068316224790]Search in Google Scholar
[20. Koller M, Muhr A. Continuous production mode as a viable process- engineering tool for efficient poly(hydroxyalkanoate) (PHA) bio-production. Chem Biochem Eng Q 2014; 28(1): 65-77.]Search in Google Scholar
[21. Koller M, Braunegg G. Potential and prospects of continuous polyhydroxyalkanoate (PHA) production. Bioengineering 2015; 2(2): 94-121.10.3390/bioengineering2020094559719528955015]Search in Google Scholar
[22. Braunegg G, Lefebvre G, Renner G, Zeiser A, Haage G, Loidl-Lanthaler K. Kinetics as a tool for polyhydroxyalkanoate production optimization. Can J Microbiol 1995: 41(13): 239-248.10.1139/m95-192]Search in Google Scholar
[23. Moser A (1988) Bioprocess technology: kinetics and reactors. Springer, New York10.1007/978-1-4613-8748-0]Search in Google Scholar
[24. Atlić A, Koller M, Scherzer D, Kutschera C, Grillo-Fernandes E, Horvat P, Chiellini E, Braunegg G. Continuous production of poly([R]-3-hydroxybutyrate) by Cupriavidus necator in a multistage bioreactor cascade. Appl Microbiol Biotechnol 2001; 91(2): 295-304.10.1007/s00253-011-3260-0]Search in Google Scholar
[25. Patnaik PR. Perspectives in the Modeling and Optimization of PHB Production by Pure and Mixed Cultures. Cit Rev Biotechnol 2005: 25(3); 153-171. 10.1080/07388550500301438]Open DOISearch in Google Scholar
[26. Koller M, Horvat P, Hesse P, Bona R, Kutschera C, Atlić A., Braunegg G. Assessment of formal and low structured kinetic modeling of polyhydroxyalkanoate synthesis from complex substrates. Bioproc Biosyst Eng 2006; 29(5-6): 367-377.10.1007/s00449-006-0084-x]Open DOISearch in Google Scholar
[27. Špoljarić IV, Lopar M, Koller M, Muhr A, Salerno A, Reiterer A, Malli K, Angerer H, Strohmeier K, Schober S, Mittelbach M. Mathematical modeling of poly[(R)-3-hydroxyalkanoate] synthesis by Cupriavidus necator DSM 545 on substrates stemming from biodiesel production. Biores Technol 2013; 133: 482-494.10.1016/j.biortech.2013.01.126]Search in Google Scholar
[28. Vadlja D, Koller M, Novak M, Braunegg G, Horvat P. Footprint area analysis of binary imaged Cupriavidus necator cells to study PHB production at balanced, transient, and limited growth conditions in a cascade process. Appl Microbiol Biotechnol 2016; 100(23): 10065-10080.10.1007/s00253-016-7844-6]Open DOISearch in Google Scholar
[29. Horvat P, Špoljarić IV, Lopar M, Atlić A, Koller M, Braunegg G. Mathematical modelling and process optimization of a continuous 5-stage bioreactor cascade for production of poly[-(R)-3-hydroxybutyrate] by Cupriavidus necator. Bioproc. Biosyst. Eng. 2013; 36(9): 1235-1250.]Search in Google Scholar
[30. Luedeking R, Piret EL. A kinetic study of the lactic acid fermentation. Batch process at controlled pH. J Biochem Microbiol Technol Eng 1959; 1(4): 393-412.10.1002/jbmte.390010406]Search in Google Scholar
[31. Megee III, RD, Drake JF, Fredrickson AG, Tsuchiya HM. Studies in intermicrobial symbiosis. Saccharomyces cerevisiae and Lactobacillus casei. Can J Microbiol 1972; 18(11): 1733-1742.10.1139/m72-269]Search in Google Scholar
[32. Mankad T, Nauman EB. Modeling of microbial growth under dual limitations. The Chem Eng J 1992; 48(2): B9-B11.10.1016/0300-9467(92)85016-3]Open DOISearch in Google Scholar
[33. Špoljarić IV, Lopar M, Koller M, Muhr A, Salerno A, Reiterer A, Horvat P. In silico optimization and low structured kinetic model of poly[(R)-3-hydroxybutyrate] synthesis by Cupriavidus necator DSM 545 by fed-batch cultivation on glycerol. J Biotechnol 2013; 168(4): 625-635.10.1016/j.jbiotec.2013.08.01924001933]Search in Google Scholar
[34. Lopar M, Špoljarić IV, Atlić A, Koller M, Braunegg G, Horvat P. Fivestep continuous production of PHB analyzed by elementary flux modes, yield space analysis and high structured metabolic model. Biochem Eng J 2013; 79, 57-70.10.1016/j.bej.2013.07.003]Open DOISearch in Google Scholar
[35. Lopar M, Špoljarić IV, Cepanec N, Koller M, Braunegg G, Horvat P. Study of metabolic network of Cupriavidus necator DSM 545 growing on glycerol by applying elementary flux modes and yield space analysis. J Ind Microbiol Biotechnol 2014; 41(6): 913-930.10.1007/s10295-014-1439-y24715530]Open DOISearch in Google Scholar
[36. Krzyzanek V, Hrubanova K, Samek O, Obruca S, Marova I, Bernatova S, Siler M, Zemanek P. Cryo-SEM and Raman Spectroscopy study of the involvement of polyhydroxyalkanoates in stress response of bacteria. Microsc Microan 2015; 21(S3): 183-184.10.1017/S1431927615001713]Search in Google Scholar
[37. Mravec F, Obruca S, Krzyzanek V, Sedlacek P, Hrubanova K, Samek O, Kucera D, Benesova P, Nebesarova J. Accumulation of PHA granules in Cupriavidus necator as seen by confocal fluorescence microscopy. FEMS Microbiol Lett 2016; 363(10), fnw094.10.1093/femsle/fnw09427190240]Search in Google Scholar
[38. Wang Y, Yin J, Chen GQ. Polyhydroxyalkanoates, challenges and opportunities. Curr Opin Biotechnol 2014; 30: 59-65.10.1016/j.copbio.2014.06.00124976377]Search in Google Scholar