Based on analysis of gene structure of mamXY operon in Magnetospirillum gryphiswaldense strain MSR-1,we constructed a mamZ deletion mutant strain(ΔmamZ)and four complemented strains with different mamZ fragment lengt...Based on analysis of gene structure of mamXY operon in Magnetospirillum gryphiswaldense strain MSR-1,we constructed a mamZ deletion mutant strain(ΔmamZ)and four complemented strains with different mamZ fragment lengths.Various cell phenotypic and physiological parameters were evaluated and compared among the wild-type(WT),mutant,and complemented strains.Cell growth rates were not notably different;however,magnetic response(Cmag)and iron uptake ability were significantly lower inΔmamZ.High-resolution transmission electron microscopy(HR-TEM)showed that magnetosomes inΔmamZ were small and irregular,and rock magnetic measurements suggested that they contained immature particles.In comparison to WT of MSR-1,intracellular iron content ofΔmamZ and the complemented strains cultured with 20mmol/L iron source was similar or slightly higher.The complemented strains were unable to synthesize mature or normal amounts of magnetosomes,apparently because of abnormal expression of the transmembrane domain of MamZ protein.Real-time reverse transcription polymerase chain reaction(RTqPCR)analysis showed that relative transcription levels of mamX and ftsZ-like genes inΔmamZ were higher at 18 h than at 12 h,suggesting that MamXY proteins play cooperative functional roles in the magnetosome maturation process.Transcription level of mms6 was significantly upregulated inΔmamZ(incubated at 12 h)and the complemented strains(incubated at 12 and 18 h),refl ecting possible interaction between MamXY and Mms6 proteins during magnetosome biosynthesis.These findings,taken together,demonstrate the essential role of MamZ in the magnetosome maturation process in MSR-1.展开更多
基金Supported by the National Natural Science Foundation of China(No.31270093)the Innovation Team of Scientific Research Platform of Anhui Province(No.KJ2015TD001)the Open Project Program of the Collaborative Innovation Center for Modern Bio-manufacture,Anhui University(No.BM2015010)。
文摘Based on analysis of gene structure of mamXY operon in Magnetospirillum gryphiswaldense strain MSR-1,we constructed a mamZ deletion mutant strain(ΔmamZ)and four complemented strains with different mamZ fragment lengths.Various cell phenotypic and physiological parameters were evaluated and compared among the wild-type(WT),mutant,and complemented strains.Cell growth rates were not notably different;however,magnetic response(Cmag)and iron uptake ability were significantly lower inΔmamZ.High-resolution transmission electron microscopy(HR-TEM)showed that magnetosomes inΔmamZ were small and irregular,and rock magnetic measurements suggested that they contained immature particles.In comparison to WT of MSR-1,intracellular iron content ofΔmamZ and the complemented strains cultured with 20mmol/L iron source was similar or slightly higher.The complemented strains were unable to synthesize mature or normal amounts of magnetosomes,apparently because of abnormal expression of the transmembrane domain of MamZ protein.Real-time reverse transcription polymerase chain reaction(RTqPCR)analysis showed that relative transcription levels of mamX and ftsZ-like genes inΔmamZ were higher at 18 h than at 12 h,suggesting that MamXY proteins play cooperative functional roles in the magnetosome maturation process.Transcription level of mms6 was significantly upregulated inΔmamZ(incubated at 12 h)and the complemented strains(incubated at 12 and 18 h),refl ecting possible interaction between MamXY and Mms6 proteins during magnetosome biosynthesis.These findings,taken together,demonstrate the essential role of MamZ in the magnetosome maturation process in MSR-1.
基金Project(50774102)supported by the National Natural Science Foundation of ChinaProject(2004CB619201)supported the National Basic Research Program of ChinaProject(1343-77341)supported by Innovative Group of Education of Graduation Student of Central South University,China
