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Ensifer adhaerens CAS22-03发酵工艺优化及D-p-HPG的酶法制备
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作者 何然峰 杨宇 +4 位作者 宋显炳 李小连 王自强 王鹏 王云山 《过程工程学报》 CAS CSCD 北大核心 2024年第9期1096-1105,共10页
为了研究Ensifer adhaerens CAS22-03来源的D-海因酶(D-Hase)与N-氨甲酰水解酶(D-Case)表达活性的影响因素,提高Ensifer adhaerens CAS22-03全细胞催化制备D-对羟基苯甘氨酸(D-p-HPG)的效率,本工作采用单因素试验和正交试验优化了Ensife... 为了研究Ensifer adhaerens CAS22-03来源的D-海因酶(D-Hase)与N-氨甲酰水解酶(D-Case)表达活性的影响因素,提高Ensifer adhaerens CAS22-03全细胞催化制备D-对羟基苯甘氨酸(D-p-HPG)的效率,本工作采用单因素试验和正交试验优化了Ensifer adhaerens CAS22-03发酵培养基的碳源、氮源,建立了Ensifer adhaerens CAS22-03的分批补料发酵工艺,分析了DHase和D-Case的酶学特性,开发了基于Ensifer adhaerens CAS22-03全细胞催化的D-p-HPG酶促生产工艺。结果表明,Ensifer adhaerens CAS22-03的最适碳源和氮源为蔗糖和酵母浸粉,分批补料发酵过程中,D-Hase和D-Case的活性高达243.6和55.8 U/g,分别提高了56.9%和46.4%。D-Hase和D-Case的最适反应温度均为45℃,最适反应pH分别为9和8。Ensifer adhaerens CAS22-03全细胞催化制备D-p-HPG的过程中,当底物浓度为40 g/L、酶用量为底物:菌体=5:1时,40℃,200 r/min条件下反应10 h,底物转化率达到95%以上,本工作的研究结果为D-p-HPG的工业酶法生产奠定了基础。 展开更多
关键词 ensifer adhaerens CAS22-03 D-海因酶 N-氨甲酰水解酶 发酵工艺优化 全细胞催化
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Enhanced cobalamin biosynthesis in Ensifer adhaerens by regulation of key genes with gradient promoters 被引量:1
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作者 Sha Xu Zhiqiang Xiao +3 位作者 Shiqin Yu Weizhu Zeng Yongming Zhu Jingwen Zhou 《Synthetic and Systems Biotechnology》 SCIE 2022年第3期941-948,共8页
Cobalamin is an essential human vitamin widely used in the pharmaceutical,food,and feed additive industries and currently produced by bacteria or archaea.Ensifer adhaerens HY-1 is an industrial strain that also produc... Cobalamin is an essential human vitamin widely used in the pharmaceutical,food,and feed additive industries and currently produced by bacteria or archaea.Ensifer adhaerens HY-1 is an industrial strain that also produces cobalamin.However production outputs are poor and the specific synthesis pathways require characterization.In this study,the whole genome sequence of E.adhaerens HY-1 was generated and annotated,and genes associated with cobalamin biosynthesis were identified.Then,three genes,CobSV,CobQ,and CobW were identified as the most efficient ones for enhancing cobalamin synthesis.By transcriptome sequencing of E.adhaerens HY-1 cells at different growth stages,65 endogenous promoters with different gradient strengths were identified.After combined expression of different strength promoters and key genes,a high cobalamin-producing recombinant strain,‘hmm’(genotype:PmetH-CobSV-PibpA-CobQ-Pmdh-CobW),was generated.Cobalamin production was 143.8 mg/L in shaking flasks,which was 41.0%higher than the original strain.Cobalamin production was further enhanced to 171.2 mg/L using fed-batch fermentation.Importantly,our data and novel approach provide important references for the analysis of cobalamin synthesis and other metabolites in complex metabolic pathways. 展开更多
关键词 ensifer adhaerens COBALAMIN Genome sequence Transcriptome sequence PROMOTER OVEREXPRESSION COMBINATIONS
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