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Genetic Analysis and Immunoelectron Microscopy of Wild and Mutant Strains of the Rubber Tree Endophytic Bacterium Serratia marcescens Strain ITBB B5–1 Reveal Key Roles of a Macrovesicle in Storage and Secretion of Prodigiosin

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Figshare2020-03-31 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Genetic_Analysis_and_Immunoelectron_Microscopy_of_Wild_and_Mutant_Strains_of_the_Rubber_Tree_Endophytic_Bacterium_i_Serratia_marcescens_i_Strain_ITBB_B5_1_Reveal_Key_Roles_of_a_Macrovesicle_in_Storage_and_Secretion_of_Prodigiosin/12113829
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Rubber tree is an economically important tropical crop. Its endophytic bacterial strain Serratia marcescens ITBB B5–1 contains an intracellular macrovesicle and red pigment. In this research, the red pigment was identified as prodigiosin by quadrupole time-of-flight mass spectrometry. Prodigiosin has a wide range of potential medical values such as anticancer and antiorgan transplant rejection. The strain ITBB B5–1 accumulated prodigiosin up to 2000 mg/L, which is higher production compared to most known Serratia strains. The formation of the macrovesicle and prodigiosin biosynthesis were highly associated and were both temporal- and temperature-dependent. A mutant strain B5–1mu that failed to produce prodigiosin was obtained by ultraviolet mutagenesis. Whole genome sequencing of wild-type and mutant strains indicated that the PigC gene encoding the last-step enzyme in the prodigiosin biosynthesis pathway was mutated in B5–1mu by a 17-bp deletion. Transmission electron microscopy analysis showed that the macrovesicle was absent in the mutant strain, indicating that formation of the macrovesicle relied on prodigiosin biosynthesis. Immunoelectron microscopy using prodigiosin-specific antiserum showed the presence of prodigiosin in the macrovesicle, the cell wall, and the extracellular vesicles, while immuno-reaction was not observed in the mutant cell. These results indicate that the macrovesicle serves as a storage organelle of prodigiosin, and secretes prodigiosin into cell envelop and culture medium as extracellular vesicles.
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2020-03-31
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