TY - JOUR
T1 - Impact of glgA1, glgA2 or glgC overexpression on growth and glycogen production in Synechocystis sp. PCC 6803
AU - Mittermair, Sandra
AU - Lakatos, Gergely
AU - Nicoletti, Cecilia
AU - Ranglová, Karolína
AU - Manoel, João Câmara
AU - Grivalský, Tomáš
AU - Kozhan, Daniyar Malikuly
AU - Masojídek, Jiří
AU - Richter, Juliane
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/11/10
Y1 - 2021/11/10
N2 - Low production rates are still one limiting factor for the industrial climate-neutral production of biovaluable compounds in cyanobacteria. Next to optimized cultivation conditions, new production strategies are required. Hence, the use of established molecular tools could lead to increased product yields in the cyanobacterial model organism Synechocystis sp. PCC6803. Its main storage compound glycogen was chosen to be increased by the use of these tools. In this study, the three genes glgC, glgA1 and glgA2, which are part of the glycogen synthesis pathway, were combined with the Pcpc560 promoter and the neutral cloning site NSC1. The complete genome integration, protein formation, biomass production and glycogen accumulation were determined to select the most productive transformants. The overexpression of glgA2 did not increase the biomass or glycogen production in short-term trials compared to the other two genes but caused transformants death in long-term trials. The transformants glgA1_11 and glgC_2 showed significantly increased biomass (1.6-fold - 1.7-fold) and glycogen production (3.5-fold - 4-fold) compared to the wild type after 96 h making them a promising energy source for further applications. Those could include for example a two-stage production process, with first energy production (glycogen) and second increased product formation (e.g. ethanol).
AB - Low production rates are still one limiting factor for the industrial climate-neutral production of biovaluable compounds in cyanobacteria. Next to optimized cultivation conditions, new production strategies are required. Hence, the use of established molecular tools could lead to increased product yields in the cyanobacterial model organism Synechocystis sp. PCC6803. Its main storage compound glycogen was chosen to be increased by the use of these tools. In this study, the three genes glgC, glgA1 and glgA2, which are part of the glycogen synthesis pathway, were combined with the Pcpc560 promoter and the neutral cloning site NSC1. The complete genome integration, protein formation, biomass production and glycogen accumulation were determined to select the most productive transformants. The overexpression of glgA2 did not increase the biomass or glycogen production in short-term trials compared to the other two genes but caused transformants death in long-term trials. The transformants glgA1_11 and glgC_2 showed significantly increased biomass (1.6-fold - 1.7-fold) and glycogen production (3.5-fold - 4-fold) compared to the wild type after 96 h making them a promising energy source for further applications. Those could include for example a two-stage production process, with first energy production (glycogen) and second increased product formation (e.g. ethanol).
KW - Cyanobacteria
KW - Energy storage
KW - Expression system
KW - Metabolic engineering
KW - Promoter
KW - Synthetic biology
KW - Glycogen
KW - Synechocystis/genetics
UR - http://www.scopus.com/inward/record.url?scp=85114839232&partnerID=8YFLogxK
U2 - 10.1016/j.jbiotec.2021.08.012
DO - 10.1016/j.jbiotec.2021.08.012
M3 - Article
C2 - 34481001
AN - SCOPUS:85114839232
SN - 0168-1656
VL - 340
SP - 47
EP - 56
JO - Journal of Biotechnology
JF - Journal of Biotechnology
ER -