表达羽田希瓦氏菌花生四烯酸9S-脂氧合酶的细胞产生C20 9S-和C22 11S-羟基脂肪酸。
Production of C20 9S- and C22 11S-hydroxy fatty acids by cells expressing Shewanella hanedai arachidonate 9S-lipoxygenase.
作者信息
Kim Min-Ju, Lee Jin, Kim Su-Eun, Shin Kyung-Chul, Oh Deok-Kun
机构信息
Department of Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea.
Department of Integrative Bioscience and Biotechnology, Konkuk University, Seoul, 05029, Republic of Korea.
出版信息
Appl Microbiol Biotechnol. 2023 Jan;107(1):247-260. doi: 10.1007/s00253-022-12285-3. Epub 2022 Nov 28.
The putative lipoxygenase (LOX) from the proteobacterium Shewanella hanedai was determined to be an 82 kDa monomeric enzyme by SDS-PAGE and gel filtration chromatography analysis. LOX was identified as a single-dioxygenating arachidonate (ARA) 9S-LOX by analyzing ARA-derived bioconversion products using high-performance liquid chromatography with reverse-, normal-, and chiral-phase columns and evaluating kinetic parameters for C20- and C22-polyunsaturated fatty acids (PUFAs). The catalytic efficiency (k/K) values of 9S-LOX from S. hanedai for ARA, eicosapentaenoic acid, and docosahexaenoic acid were 3.1-, 4.1-, and 2.5-fold higher, respectively, than those only reported 9S-LOX from Sphingopyxis macrogoltabida with double-dioxygenating activity. To promote the production of C20 9S- and C22 11S-hydroxy fatty acids (HFAs) using Escherichia coli expressing 9S-LOX from S. hanedai, bioconversion conditions, including temperature, pH, solvent type and its concentration, concentrations of cells, and substrate, were optimized to 25 °C, pH 8.5, 6% (v/v) dimethyl sulfoxide, 0.2 g/l cells, and 7 mM ARA as substrate in a 500 ml-Erlenmeyer baffled flask with 50 ml reaction solution with agitation at 200 rpm in the presence of 10 mM cysteine as a reduction agent, respectively. Under these conditions, 6.4 mM 9S-hydroxyeicosatetraenoic acid, 6.2 mM 9S-hydroxyeicosapentaenoic acid, and 5.9 mM 11S-hydroxydocosahexaenoic acid were produced in 30 min, 40 min, and 60 min with specific productivities of 1067 μmol/min/g, 775 μmol/min/g, and 492 μmol/min/g, volumetric productivities of 213 μM/min, 155 μM/min, and 98 μM/min, and conversion yields of 91.4%, 88.6%, and 84.3%, respectively. To date, these are the highest specific productivities reported for the bioconversion of C20- and C22-PUFAs into HFAs. KEY POINTS: • Lipoxygenase from Shewanella hanedai was identified as arachidonate 9S-lipoxygenase • Optimization led to increased production of C20 9S- and C22 11S-hydroxy fatty acids • We reported the highest specific productivities of C20- and C22-hydroxy fatty acids.
通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和凝胶过滤色谱分析,确定来自汉氏希瓦氏菌(Shewanella hanedai)的假定脂氧合酶(LOX)是一种82 kDa的单体酶。通过使用反相、正相和手性相柱的高效液相色谱分析花生四烯酸(ARA)衍生的生物转化产物,并评估C20和C22多不饱和脂肪酸(PUFA)的动力学参数,LOX被鉴定为单加双氧的花生四烯酸9S-脂氧合酶。汉氏希瓦氏菌9S-脂氧合酶对ARA、二十碳五烯酸和二十二碳六烯酸的催化效率(k/K)值分别比仅报道的具有双加双氧活性的大球鞘氨醇单胞菌(Sphingopyxis macrogoltabida)9S-脂氧合酶高3.1倍、4.1倍和2.5倍。为了利用表达汉氏希瓦氏菌9S-脂氧合酶的大肠杆菌促进C20 9S-和C22 11S-羟基脂肪酸(HFA)的生产,在装有50 ml反应溶液的500 ml三角瓶中,以10 mM半胱氨酸作为还原剂,在200 rpm搅拌条件下,将生物转化条件(包括温度、pH、溶剂类型及其浓度、细胞浓度和底物)分别优化为25°C、pH 8.5、6%(v/v)二甲基亚砜、0.2 g/l细胞和7 mM ARA作为底物。在这些条件下,分别在30分钟、40分钟和60分钟内产生了6.4 mM 9S-羟基二十碳四烯酸、6.2 mM 9S-羟基二十碳五烯酸和5.9 mM 11S-羟基二十二碳六烯酸,比生产率分别为1067 μmol/min/g、775 μmol/min/g和492 μmol/min/g,体积产率分别为213 μM/min、155 μM/min和98 μM/min,转化率分别为91.4%、88.6%和84.3%。迄今为止,这些是将C20和C22多不饱和脂肪酸生物转化为羟基脂肪酸所报道的最高比生产率。要点:• 汉氏希瓦氏菌的脂氧合酶被鉴定为花生四烯酸9S-脂氧合酶 • 优化提高了C20 9S-和C22 11S-羟基脂肪酸的产量 • 我们报道了C20和C22羟基脂肪酸的最高比生产率