Effects of Reduced and Enhanced Glycogen Pools on Salt-Induced Sucrose Production in a Sucrose-Secreting Strain of Synechococcus elongatus PCC 7942

• Published in: Applied and environmental microbiology 2018-01, Vol.84 (2)
• Main Authors: Qiao, Cuncun, Duan, Yangkai, Zhang, Mingyi, Hagemann, Martin, Luo, Quan, Lu, Xuefeng
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - genetics; Biotechnology; Carbohydrate Metabolism; Carbohydrates; Carbon; Carbon - metabolism; Chemical synthesis; Cyanobacteria; Down-Regulation; Effects; Elongation; Gene expression; Glucose-1-phosphate; Glucosyltransferases - metabolism; Glycogen; Glycogen - analysis; Glycogen - biosynthesis; Glycogen - genetics; Glycogen - metabolism; Metabolic Engineering - methods; Phosphates; Riboswitch; Salt; Salts; Sodium Chloride - pharmacology; Strain; Stress response; Sucrose; Sucrose - analysis; Sucrose - metabolism; Sucrose-phosphate synthase; Sugar; Synechococcus - drug effects; Synechococcus - genetics; Synechococcus - metabolism; Synechococcus elongatus; Theophylline
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.02023-17

Sucrose and glycogen syntheses in cyanobacteria share the common precursor glucose-1-phosphate. It is generally assumed that lowering glycogen synthesis could drive more carbon toward sucrose synthesis that can be induced by salt stress among cyanobacteria. By using a theophylline-dependent riboswitch system, the expression of , a key gene in glycogen synthesis, was downregulated in a quantitative manner in a sucrose-secreting strain of PCC 7942. We observed that the stepwise suppression of glycogen synthesis limited rather than stimulated sucrose production in the salt-stressed cells, suggesting that glycogen could serve as a carbon pool for the synthesis of sucrose. Accordingly, we generated glycogen-overproducing strains, but the increased glycogen pool alone did not stimulate sucrose production, indicating that alternative steps limit the carbon flux toward the synthesis of sucrose. Consistent with previous studies that showed that sucrose-phosphate synthase (SPS) catalyzes the rate-limiting step in sucrose synthesis, the combination of glycogen overproduction and overexpression resulted in increased sucrose production. Our results indicate that the glycogen and sucrose pools are closely linked in PCC 7942, and we propose that enhancing the glycogen pool could be a promising strategy for the improvement of sucrose production by cyanobacteria in the presence of a strong sucrose synthesis sink. Many cyanobacteria naturally synthesize and accumulate sucrose when stressed by NaCl, which provides novel possibilities for obtaining sugar feedstock by engineering of cyanobacteria. It has been assumed that glycogen synthesis competes with sucrose synthesis for the carbon flux. However, our results showed that the suppression of glycogen synthesis decreased rather than stimulated sucrose production in a sucrose-secreting strain of PCC 7942. This result suggests that glycogen could serve as a supportive rather than a competitive carbon pool for the synthesis of sucrose, providing new insights about the relation between glycogen synthesis and sucrose synthesis in cyanobacteria. This finding is also useful to guide metabolic engineering work to optimize the production of sucrose and possibly other products by cyanobacteria.