Jingnan Wang’s research while affiliated with Beijing Institute of Technology and other places

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Publications (4)


Fermentation profiles of ASAGF58 and high-yield strain H2. a The process of mutant strain screening and validation. b Lethality rate and mutation rate of S. pogona. c Comparison of butenyl-spinosyn production in ASAGF58 and H2. d Comparison of glucose consumption between ASAGF58 and H2. e The biomass of ASAGF58 and H2
Transcription analysis of ASAGF58 and H2. a Comparative transcriptome analysis of the DEGs between ASAGF58 and H2. b-d Bubble plot of the significant pathways with KEGG enrichment of DEGs at 72, 120, and 192 h, respectively
The differences in pivotal metabolic pathways between H2 and ASAGF58 in the ribosome, oxidative phosphorylation, and purine metabolism pathways. The heatmap colors represent gene expression levels (Log2FC) for each sample, as indicated in the legend on the right. PRPP: phosphoribosyl pyrophosphate, PRA: 5-phosphoribosylamine, GAR: 5’-phosphoribosylglycinamide, FGAR: 5’-phosphoribosyl-N-formylglycinamide, FGAM: 2-(formamido)-N1-(5’-phosphoribosyl) acetamidine, AIR: aminoimidazole ribotide, CAIR: 1-(5-phospho-D-ribosyl)−5-amino-4-imidazolecarboxylate, SAICAR: 1-(5’-phosphoribosyl)−5-amino-4-(N-succinocarboxamide)-imidazole, AICAR: 1-(5’-phosphoribosyl)−5-amino-4-imidazolecarboxamide, FAICAR: 1-(5’-phosphoribosyl)−5-formamido-4-imidazolecarboxamide, IMP: inosine monophosphate, XMP: xanthosine monophosphate, GMP: guanosine monophosphate, GDP: guanosine diphosphate, GTP: gnosine 5’-triphosphate, AMP: adenosine monophosphate, ADP: adenosine 5’-diphosphate, ATP: adenosine 5’-triphosphate, purF: gutamine phosphoribosyl pyrophosphate amidotransferase, purD: phosphoribosylglycinamide synthetase, purN: phosphoribosylglycinamide formyltransferase, purS/L/Q: phosphoribosylformylglycinamidine synthase, purM: phosphoribosylaminoimidazole synthetase, purC: phosphoribosylaminoimidazole-succinocarboxamide synthetase, purB: adenylosuccinate lyase, purH: phosphoribosylaminoimidazolecarboxamide formyltransferase, guaB: IMP dehydrogenase, guaA: guanylate synthetase, gmk: guanylate kinase, adk: adenylate kinase, pyk: pyruvate kinase, hpt: hypoxanthine phosphoribosyltransferase, apt: adenine phosphoribosyltransferase, rpsA/B/C/D/E/F/G/H/I/J/K/L/M/N/O/P/Q/R2/S/T: 30S ribosomal protein, atpA/B/C/D/E/F/G/H: ATP synthase, sdhA/B/C/D: succinate dehydrogenase, nuoA/B/C/D/E/F/G/H/I/J/K/L/M/N: NADH dehydrogenase, cydA/B: cytochrome d oxidase subunit, cyoE: heme o synthase, qcrB/C: cytochrome c reductase, coxA/B/C: cytochrome c oxidase
The function validation of 20 transcriptional regulators. a Flowchart of the functional validation of transcriptional regulators. b The production of butenyl-spinosyn in transcriptional regulator overexpression strain
The effect of TF00350 on the growth and metabolism of S. pogona. a Comparison of butenyl-spinosyn production between ASAGF58 and RS00350. b Gene expression levels of the butenyl-spinosyn biosynthetic gene. busA/B/C/D/E: polyketide synthase, busJ: dehydrogenase, busM/L: cyclase, busF: [4 + 2]-carbocyclases, busG: rhamnosyltransferase, busH/I/K: O-methyl-transferase, busN: 3-ketoreductase, busO: 2,3-dehydratase, busP: forosamyltransferase, busQ: 3,4-dehydratase, busR: transaminase, busS: dimethyltransferase, epi: 3′5’-epimerase, gdh: NDP-glucose-dehydratase, gtt: NDP-glucose synthase, kre: 4’-ketoreductase. c Mycelial morphology comparison between ASAGF58 and RS00350 at 72 and 120 h. d Growth curve analysis and (e) Glucose consumption of ASAGF58 and RS00350

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The PurR family transcriptional regulator promotes butenyl-spinosyn production in Saccharopolyspora pogona
  • Article
  • Full-text available

January 2025

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43 Reads

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1 Citation

Applied Microbiology and Biotechnology

Xinying Li

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Jingnan Wang

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Chang Su

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Butenyl-spinosyn, derived from Saccharopolyspora pogona, is a broad-spectrum and effective bioinsecticide. However, the regulatory mechanism affecting butenyl-spinosyn synthesis has not been fully elucidated, which hindered the improvement of production. Here, a high-production strain S. pogona H2 was generated by Cobalt-60 γ-ray mutagenesis, which showed a 2.7-fold increase in production compared to the wild-type strain S. pogona ASAGF58. A comparative transcriptomic analysis between S. pogona ASAGF58 and H2 was performed to elucidate the high-production mechanism that more precursors and energy were used to synthesize of butenyl-spinosyn. Fortunately, a PurR family transcriptional regulator TF00350 was discovered. TF00350 overexpression strain RS00350 induced morphological differentiation and butenyl-spinosyn production, ultimately leading to a 5.5-fold increase in butenyl-spinosyn production (141.5 ± 1.03 mg/L). Through transcriptomics analysis, most genes related to purine metabolism pathway were downregulated, and the butenyl-spinosyn biosynthesis gene was upregulated by increasing the concentration of c-di-GMP and decreasing the concentration of c-di-AMP. These results provide valuable insights for further mining key regulators and improving butenyl-spinosyn production. Key points • A high production strain of S. pogona H2 was obtained by⁶⁰Co γ-ray mutagenesis. • Positive regulator TF00350 identified by transcriptomics, increasing butenyl-spinosyn production by 5.5-fold. • TF00350 regulated of butenyl-spinosyn production by second messengers.

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Breeding and modification strategies of butenyl-spinosyn high-yield strains

April 2022

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1 Read

Butenyl-spinosyn is an insecticide produced by Saccharopolyspora pogona, which has both the safety of biological pesticides and the quick-acting properties of chemical pesticides. However, the low synthesis efficiency of butenyl-spinosyn by wild-type strains cannot meet the need of industrial production, obtaining high-yield strains is an urgent problem. At present, there are few related studies on butenyl-spinosyn. The spinosyn produced by Saccharopolyspora spinosa has a similar structural and biosynthetic pathway. This article describes the basic characteristics of them, draws on the research experience of spinosyn, summarizes the available strategies for breeding and modifying high-yield butenyl-spinosyn strains, including mutagenesis methods and precise genetic engineering methods such as metabolic flux regulation, pathway genes regulation, transcriptional regulation, heterologous expression, which may provide ideas for further research of butenyl-spinosyn.


Citations (2)


... Common strategies to improve S. cerevisiae's tolerance to environmental stress include evolutionary engineering, genome shuffling, and global transcriptional regulation mechanisms [12]. Advances in functional genomics, transcriptomics, and metabolomics offer new avenues for strain transformation, with synthetic biology providing a framework for designing and constructing artificial biological systems at the molecular level [13,14]. ...

Reference:

Effect of Over-expression of GRXs on Thermo and Acetic Acid Stress Tolerance of Saccharomyces cerevisiae
Intelligent microbial cell factory with tolerance for green biological manufacturing
  • Citing Article
  • August 2020

... Metabolic pathways interact with each other, forming a complex metabolic network. Many studies have sought to elucidate regulation mechanisms and enhance production using advanced omics-based technologies [12][13][14][15][16]. ...

Exploring a High-Efficiency Genetic Transformation System for Engineering Saccharopolyspora pogona ASAGF58 To Improve Butenyl-Spinosyn Production
  • Citing Article
  • February 2023

ACS Agricultural Science & Technology