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Comparative transcriptomics ofBacillus thuringiensis Bt4.0718 reveals the mechanisms of sporulation and parasporal crystal formation
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Junyan XIE1, 2, Sisi LUO1, Zirong ZHU1, Wenhui CHEN1, Kexuan ZHOU1, Liqiu XIA1, Xuezhi DING1, *
Acta Microbiologica Sinica | 2024, 64(1) : 108 - 129
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Acta Microbiologica Sinica | 2024, 64(1): 108-129
Research Articles
Comparative transcriptomics ofBacillus thuringiensis Bt4.0718 reveals the mechanisms of sporulation and parasporal crystal formation
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Junyan XIE1, 2, Sisi LUO1, Zirong ZHU1, Wenhui CHEN1, Kexuan ZHOU1, Liqiu XIA1, Xuezhi DING1, *
Affiliations
  • 1 Hunan Provincial Key Laboratory of Microbial Molecular Biology, State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha 410081, Hunan, China
  • 2 National Engineering Laboratory for Pollution Control and Waste Utilization in Livestock and Poultry Production, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, Hunan, China
Published: 2024-01-04 doi: 10.13343/j.cnki.wsxb.20230213
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[Objective] Bacillus thuringiensis (Bt), characterized by the massive production of insecticidal crystal proteins (ICPs) during sporulation, serves as the main strain resource for the commonly used and safe microbial insecticides. To further explore the mechanisms of sporulation and parasporal crystal formation and lay a theoretical foundation for the construction of efficient strains, we compared the transcriptomes of Bt at three important stages.[Methods] The transcriptomes of the hypervirulent strain Bt4.0718 at the middle vegetative growth stage (T1-10 h), the early sporulation stage (T2-20 h), and the late sporulation stage (T3-32 h) were compared. The representative differentially expressed genes (DEGs) were verified by real-time fluorescence quantitative PCR (qRT-PCR), and the phenotypes of the mutant strains with the knockout of specific functional genes were examined.[Results] The number of DEGs was 2 147 (T2/T1), 1 861 (T3/T1), and 1 708 (T3/T2), respectively. At T1, the medium was rich in nutrients, which served the sporulation and parasporal crystal formation. The high transcription levels ofkinA/D,spo0A/F, andsigE regulating sporulation played a role in the growth and development of the cells. The transcription of Cry1Ac, poly-hydroxybutyric acid (PHB), and hydroxybutanone (acetoin) were started at this time. The substantial formation of ICPs and spores occurred at T2 and T3, and the transcript levels of the regulatory genes were higher at T2 than those at T3. The genes associated with spore core/coat/cortex, germination protein, andspoII–spoVI began to be transcribed in large amounts at T2, with the highest levels among the three stages. The corresponding complex networks of carbohydrate, amino acid, and lipid metabolism, energy, nucleic acid, and peptide metabolism, secondary metabolite production, and environmental adaptation showed differences. In addition, as the physiological processes stimulated by nutrient signals, the two-component signal transduction system (TCS) and ABC transport system played an essential role in the process of sporulation and ICP transcription and expression, and their transcription levels were significantly different.[Conclusion] With the production of ICPs and sporulation, nutrients are gradually consumed, and the high expression ofsigB,sigW, andsigM contributed to the stability of cell wall and the resistance to environmental changes. Meanwhile, the small heat shock proteins Hsp20 and Hsp20B, as molecular chaperones, were also important for maintaining intracellular homeostasis and may facilitate the sporulation and ICP production.

Bacillus thuringiensis  /  comparative transcriptomics  /  sporulation  /  insecticidal parasporal crystals
Junyan XIE, Sisi LUO, Zirong ZHU, Wenhui CHEN, Kexuan ZHOU, Liqiu XIA, Xuezhi DING. Comparative transcriptomics ofBacillus thuringiensis Bt4.0718 reveals the mechanisms of sporulation and parasporal crystal formation[J]. Acta Microbiologica Sinica, 2024 , 64 (1) : 108 -129 . DOI: 10.13343/j.cnki.wsxb.20230213
  • National Key Research and Development Program of China(2017YFD0201201)
  • National Natural Science Foundation of China(31370116)
Year 2024 volume 64 Issue 1
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doi: 10.13343/j.cnki.wsxb.20230213
  • Receive Date:2023-03-30
  • Online Date:2026-03-18
  • Published:2024-01-04
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History
  • Received:2023-03-30
  • Accepted:2023-09-27
Funding
National Key Research and Development Program of China(2017YFD0201201)
National Natural Science Foundation of China(31370116)
Affiliations
    1 Hunan Provincial Key Laboratory of Microbial Molecular Biology, State Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Sciences, Hunan Normal University, Changsha 410081, Hunan, China
    2 National Engineering Laboratory for Pollution Control and Waste Utilization in Livestock and Poultry Production, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, Hunan, China

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*DING Xuezhi, E-mail:
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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