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陈柏楠, 余胜超, 袁丽, 杨明坤, 葛峰. 鱼腥藻PCC 7120乙酰辅酶A合成酶All0769的缺失降低异形胞频率[J]. 水生生物学报, 2023, 47(7): 1025-1035. DOI: 10.7541/2023.2022.0419
引用本文: 陈柏楠, 余胜超, 袁丽, 杨明坤, 葛峰. 鱼腥藻PCC 7120乙酰辅酶A合成酶All0769的缺失降低异形胞频率[J]. 水生生物学报, 2023, 47(7): 1025-1035. DOI: 10.7541/2023.2022.0419
CHEN Bai-Nan, YU Sheng-Chao, YUAN Li, YANG Ming-Kun, GE Feng. THE LOSS OF ACETYL COENZYME A SYNTHETASE ALL0769 REDUCES THE FREQUENCY OF HETEROCYSTS IN ANABAENA SP. PCC 7120[J]. ACTA HYDROBIOLOGICA SINICA, 2023, 47(7): 1025-1035. DOI: 10.7541/2023.2022.0419
Citation: CHEN Bai-Nan, YU Sheng-Chao, YUAN Li, YANG Ming-Kun, GE Feng. THE LOSS OF ACETYL COENZYME A SYNTHETASE ALL0769 REDUCES THE FREQUENCY OF HETEROCYSTS IN ANABAENA SP. PCC 7120[J]. ACTA HYDROBIOLOGICA SINICA, 2023, 47(7): 1025-1035. DOI: 10.7541/2023.2022.0419

鱼腥藻PCC 7120乙酰辅酶A合成酶All0769的缺失降低异形胞频率

THE LOSS OF ACETYL COENZYME A SYNTHETASE ALL0769 REDUCES THE FREQUENCY OF HETEROCYSTS IN ANABAENA SP. PCC 7120

  • 摘要: 研究鉴定了All0769为鱼腥藻PCC 7120中乙酰辅酶A合成酶, 通过CRISPR/Cpf1系统敲除鱼腥藻PCC 7120中的乙酰辅酶A合成酶(由all0769编码), 探究了乙酰辅酶A合成酶在异形胞分化中的调控机制。结果所示: All0769能在体外反应中催化乙酰辅酶A的生成。在供氮环境下, 敲除all0769会影响藻细胞生长速率。而无论环境中是否存在化合氮, Δall0769突变株的乙酰辅酶A和α-酮戊二酸含量均显著减少。在供氮环境下, Δall0769突变株中检测到(26.17±1.55) nmol/mg protein的乙酰辅酶A, 而在野生型中检测出(43.04±1.09) nmol/mg的乙酰辅酶A。Δall0769突变株的α-酮戊二酸(1.41±0.24) nmol/mg protein低于野生型的α-酮戊二酸(2.13±0.05) nmol/mg protein。在缺氮环境下, Δall0769突变株中检测到(10.00±2.81) nmol/mg protein的乙酰辅酶A, 而在野生型中检测出(29.82±4.04) nmol/mg protein的乙酰辅酶A。Δall0769突变株的α-酮戊二酸含量(1.48±0.35) nmol/mg protein低于野生型的α-酮戊二酸(2.74±0.33) nmol/mg protein。此外, Δall0769突变株异形胞分化频率(7.12%)显著低于野生型异形胞分化频率(9.22%)。综上所述: 文章鉴定了All0769是鱼腥藻PCC 7120中的乙酰辅酶A合成酶。在鱼腥藻PCC 7120中, 缺失乙酰辅酶A合成酶(All0769)会减少乙酰辅酶A的含量, 进而下调α-酮戊二酸含量使异形胞频率降低。

     

    Abstract: In this study, we identified All0769 as acetyl coenzyme A (acetyl-CoA) synthetase in Anabaena sp. PCC 7120, and investigated the molecular mechanism of acetyl coenzyme A syntheses (encoded by all0769) in the regulation of heterocyst differentiation in Anabaena sp. PCC 7120 by disrupting all0769 with a CRISPR/Cpf1 system. Our results demonstrated that All0769 could catalyze the formation of acetyl-CoA in vitro and loss of the all0769 was found to affect the growth of Anabaena sp. PCC 7120 cells under combined nitrogen. The content of acetyl-CoA and α-ketoglutaric acid were significantly decreased in Δall0769 strain compared to that of WT under combined nitrogen and nitrogen deficiency conditions. We detected (26.17±1.55) nmol/mg protein acetyl-CoA in Δall0769 strain, whereas (43.04±1.09) nmol/mg protein acetyl-CoA was obtained in wild-type strain under combined nitrogen. For the content of α-ketoglutaric acid, Δall0769 strain exhibited a decrease α-ketoglutaric acid (1.41±0.24) nmol/mg protein relative to that of WT (2.13±0.05) nmol/mg protein under combined nitrogen. Upon deprivation of combined nitrogen, we measured (10.00±2.81) nmol/mg protein acetyl-CoA in Δall0769 strain, while (29.82±4.04) nmol/mg protein acetyl-CoA was received in wild-type strain. Additionally, the content of α-ketoglutaric acid decreased in the Δall0769 strain (1.48±0.35) nmol/mg protein, compared with the wild-type strain (2.74±0.33) nmol/mg protein after the removal of combined nitrogen. Furthermore, the heterocyst formation was measured and Δall0769 strain shows a significant difference in heterocyst frequency (7.12%) compared with the wild-type (9.22%) at 24h. In conclusion, we identified All0769 as acetyl coenzyme A (acetyl-CoA) synthetase in Anabaena sp. PCC 7120. And All0769 deletion led to impaired growth, content of acetyl-CoA, α-ketoglutaric acid and heterocyst frequency in Anabaena sp. PCC 7120.

     

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