A promising bacterial strain for the biodegradation of Microcystins(MCs)was isolated from Dianchi lake in China and identified as Sphingopyxis sp.USTB-05 by the analysis of 16s rDNA.Initial MC-RR of 42.3 mg·L -1 ...A promising bacterial strain for the biodegradation of Microcystins(MCs)was isolated from Dianchi lake in China and identified as Sphingopyxis sp.USTB-05 by the analysis of 16s rDNA.Initial MC-RR of 42.3 mg·L -1 was completely degraded by USTB-05 within 36 h,which was a relatively high biodegradation rate of MC-RR.With the cell-free extract(CE)of Sphingopyxis sp.USTB-05,MC-RR was biodegraded at a more rapid biodegradation rate compared with its strain,so that initial MC-RR of 42.3 mg·L -1 was completely biodegraded within 10 h.During the bio-reaction of MC-RR catalyzed by CE,two intermediate metabolites and a dead-end product of MC-RR were observed on HPLC profiles and all of them had similar scanning profiles in the wavelength from 200 to 300 nm,indicating that the group of Adda in all products of MC-RR remained intact.展开更多
Harmful cyanobacterial blooms are a growing environmental problem worldwide in natural waters, the biodegradation is found to be the most efficient method for removing microcystins 0VICs） produced by harmful cyanobac...Harmful cyanobacterial blooms are a growing environmental problem worldwide in natural waters, the biodegradation is found to be the most efficient method for removing microcystins 0VICs） produced by harmful cyanobacteria. Based on the isolation of a promising bacterial strain of Sphingopyxis sp. USTB-05 for biodegrading MCs, we for the first time cloned and expressed a gene USTB-O5-A （HM245411） that is responsible for the first step in the biodegradation of microcystin LR （MC-LR） in E. coli DH5ct, with a cloning vector of pGEM-T easy and an expression vector of pGEX-4T-1, respectively. The cell-free extracts （CE） of recombinant E. coli DH5ct containing USTB-O5-A had high activity for biodegrading MC-LR. The initial MC-LR concentration of 40 mg/L was completely biodegraded within 1 hr in the presence of CE with a protein concentration of 0.35 mg/mL. Based on an analysis of the liquid chromatogram-mass spectrum （LC-MS）, the enzyme encoded by gene USTB-O5-A was found to be active in cleaving the target peptide bond between 3-amino-9-methoxy-2,6, 8-trimethyl-10-phenyl-deca-4,6-dienoic acid （Adda） and arginine of MC-LR, and converting cyclic MC-LR to linear MC-LR as a first product that is much less toxic than parent MC-LR, which offered direct evidence for the first step on the pathway of MC-LR biodegradation by Sphingopyxis sp. USTB-05.展开更多
A strain, USTB-05, isolated from Lake Dianchi, China, degraded the cyanobacterial toxin microcystin-RR （MC-RR） at the rate of 16.7 mg/L per day. Analysis of 16S rDNA sequence showed that the strain was Sphingopyxis ...A strain, USTB-05, isolated from Lake Dianchi, China, degraded the cyanobacterial toxin microcystin-RR （MC-RR） at the rate of 16.7 mg/L per day. Analysis of 16S rDNA sequence showed that the strain was Sphingopyxis sp. Enzymatic degradation pathways for MC-RR by Sphingopyxis sp. USTB-05 were identified. Adda-Arg peptide bond of MC-RR was cleaved and then a hydrogen and a hydroxyl were combined onto the NH2 group of Adda and the carboxyl group of arginine to form a linear molecule as intermediate product within the first few hours. Then, through dehydration reaction, two hydrogen of amino group on arginine reacted with adjacent hydroxyl on carbon to form a linear MC-RR with two small peptide rings as the final product after 24 hr. These biodegradation pathways were different from those reported for other strains, implying that MC-RR may undergo different transformations and different products were formed due to various bacteria in natural lakes and reservoirs.展开更多
A promising bacterial strain for biodegradingmicrocystin-LR(MC-LR)as the sole carbon and nitrogensource was successfully isolated from Lake Dianchi,China.The strain was identified as Sphingopyxis sp.USTB-05,which was ...A promising bacterial strain for biodegradingmicrocystin-LR(MC-LR)as the sole carbon and nitrogensource was successfully isolated from Lake Dianchi,China.The strain was identified as Sphingopyxis sp.USTB-05,which was the first isolated MCs-biodegradingSphingopyxis sp.in China.The average biodegradationrate of MC-LR by Sphingopyxis sp.USTB-05 was 28.8mg·L^(-1)per day,which was apparently higher than those ofother bacteria reported so far.The optimal temperature andpH for both strain USTB-05 growth and MC-LRbiodegradation were 30℃and 7.0,respectively.Therelease of MC-LR from the cyanobacterial cells collectedfrom Lake Guishui and the biodegradation of MC-LR byboth strain and cell-free extract(CE)were investigated.The results indicated that MC-LR with the initialconcentration of 4.0 mg·L^(-1)in water was biodegraded bySphingopyxis sp.USTB-05 within 4 d,while MC-LR withthe initial concentration of 28.8 mg·L^(-1)could be completelyremoved in 3 h by CE of Sphingopyxis sp.USTB-05 containing 350 mg·L^(-1)protein.During enzymaticbiodegradation of MC-LR,two intermediate metabolitesand a dead-end product were observed on an HPLCchromatogram.Moreover,the similar scanning profiles ofMC-LR and its metabolic products indicate that the Addaside-chain of MC-LR was kept intact in all products.展开更多
A promising microalgal strain isolated from fresh water,which can grow both autotrophically on inorganic carbon under lighting and heterotrophically on organic carbon without lighting,was identified as Chlorella sp.US...A promising microalgal strain isolated from fresh water,which can grow both autotrophically on inorganic carbon under lighting and heterotrophically on organic carbon without lighting,was identified as Chlorella sp.USTB-01 with the phylogenetic analysis based on 18S ribosomal ribonucleic acid(rRNA)gene sequences.In the heterotrophic batch culture,more than 20.0 g·L^(-1)of cell dry weight concentration(DWC)of Chlorella sp.USTB-01 was obtained at day 5,and which was used directly to seed the autotrophic culture.A novel fermentor-helical combined photobioreactor was established and used to cultivate Chlorella sp.USTB-01 for the fixation of carbon dioxide(CO_(2)).It showed that the autotrophic growth of Chlorella sp.USTB-01 in the combined photobioreactor was more effective than that in the fermentor alone and the maximum DWC of 2.5 g·L^(-1)was obtained at day 6.The highest CO_(2)fixation of 95%appeared on day 1 in the exponential growth phases of Chlorella sp.USTB-01 and 49.8%protein was found in the harvested microalgal cells.展开更多
基金Supported by the State Key Development Program for Basic Research of China（2008CB418105） the National Natural Science Foundation of China（203777008 20621703）+1 种基金 the State Key Joint Laboratory of Environment Simulation and Pollution Control（09K08ESPCT） the Educational Committee of Beijing
文摘A promising bacterial strain for the biodegradation of Microcystins(MCs)was isolated from Dianchi lake in China and identified as Sphingopyxis sp.USTB-05 by the analysis of 16s rDNA.Initial MC-RR of 42.3 mg·L -1 was completely degraded by USTB-05 within 36 h,which was a relatively high biodegradation rate of MC-RR.With the cell-free extract(CE)of Sphingopyxis sp.USTB-05,MC-RR was biodegraded at a more rapid biodegradation rate compared with its strain,so that initial MC-RR of 42.3 mg·L -1 was completely biodegraded within 10 h.During the bio-reaction of MC-RR catalyzed by CE,two intermediate metabolites and a dead-end product of MC-RR were observed on HPLC profiles and all of them had similar scanning profiles in the wavelength from 200 to 300 nm,indicating that the group of Adda in all products of MC-RR remained intact.
基金supported by the National Natural Science Foundation of China (No. 21177009)
文摘Harmful cyanobacterial blooms are a growing environmental problem worldwide in natural waters, the biodegradation is found to be the most efficient method for removing microcystins 0VICs） produced by harmful cyanobacteria. Based on the isolation of a promising bacterial strain of Sphingopyxis sp. USTB-05 for biodegrading MCs, we for the first time cloned and expressed a gene USTB-O5-A （HM245411） that is responsible for the first step in the biodegradation of microcystin LR （MC-LR） in E. coli DH5ct, with a cloning vector of pGEM-T easy and an expression vector of pGEX-4T-1, respectively. The cell-free extracts （CE） of recombinant E. coli DH5ct containing USTB-O5-A had high activity for biodegrading MC-LR. The initial MC-LR concentration of 40 mg/L was completely biodegraded within 1 hr in the presence of CE with a protein concentration of 0.35 mg/mL. Based on an analysis of the liquid chromatogram-mass spectrum （LC-MS）, the enzyme encoded by gene USTB-O5-A was found to be active in cleaving the target peptide bond between 3-amino-9-methoxy-2,6, 8-trimethyl-10-phenyl-deca-4,6-dienoic acid （Adda） and arginine of MC-LR, and converting cyclic MC-LR to linear MC-LR as a first product that is much less toxic than parent MC-LR, which offered direct evidence for the first step on the pathway of MC-LR biodegradation by Sphingopyxis sp. USTB-05.
基金supported by the Chinese National Key Project for Basic Research (No.2008CB418105)the National Natural Science Foundation of China(No.20621703,20477050)the Important-Direction-Project funded by the Chinese Academy of Sciences
文摘A strain, USTB-05, isolated from Lake Dianchi, China, degraded the cyanobacterial toxin microcystin-RR （MC-RR） at the rate of 16.7 mg/L per day. Analysis of 16S rDNA sequence showed that the strain was Sphingopyxis sp. Enzymatic degradation pathways for MC-RR by Sphingopyxis sp. USTB-05 were identified. Adda-Arg peptide bond of MC-RR was cleaved and then a hydrogen and a hydroxyl were combined onto the NH2 group of Adda and the carboxyl group of arginine to form a linear molecule as intermediate product within the first few hours. Then, through dehydration reaction, two hydrogen of amino group on arginine reacted with adjacent hydroxyl on carbon to form a linear MC-RR with two small peptide rings as the final product after 24 hr. These biodegradation pathways were different from those reported for other strains, implying that MC-RR may undergo different transformations and different products were formed due to various bacteria in natural lakes and reservoirs.
基金The first and second authors did same contribution to this paper.This work was supported by the National Natural Science Foundation of China(Grant No.203777008)State Key Joint Laboratory of Environment Simulation and Pollution Control(No.09K08ESPCT),and Educational Committee of Beijing.
文摘A promising bacterial strain for biodegradingmicrocystin-LR(MC-LR)as the sole carbon and nitrogensource was successfully isolated from Lake Dianchi,China.The strain was identified as Sphingopyxis sp.USTB-05,which was the first isolated MCs-biodegradingSphingopyxis sp.in China.The average biodegradationrate of MC-LR by Sphingopyxis sp.USTB-05 was 28.8mg·L^(-1)per day,which was apparently higher than those ofother bacteria reported so far.The optimal temperature andpH for both strain USTB-05 growth and MC-LRbiodegradation were 30℃and 7.0,respectively.Therelease of MC-LR from the cyanobacterial cells collectedfrom Lake Guishui and the biodegradation of MC-LR byboth strain and cell-free extract(CE)were investigated.The results indicated that MC-LR with the initialconcentration of 4.0 mg·L^(-1)in water was biodegraded bySphingopyxis sp.USTB-05 within 4 d,while MC-LR withthe initial concentration of 28.8 mg·L^(-1)could be completelyremoved in 3 h by CE of Sphingopyxis sp.USTB-05 containing 350 mg·L^(-1)protein.During enzymaticbiodegradation of MC-LR,two intermediate metabolitesand a dead-end product were observed on an HPLCchromatogram.Moreover,the similar scanning profiles ofMC-LR and its metabolic products indicate that the Addaside-chain of MC-LR was kept intact in all products.
基金This research was supported by PetroChina Innovation Foundation(2009D-5006-04-02)the Fundamental Research Funds for the Central Universities and the Metallurgical Foundation of University of Science and Technology Beijing.
文摘A promising microalgal strain isolated from fresh water,which can grow both autotrophically on inorganic carbon under lighting and heterotrophically on organic carbon without lighting,was identified as Chlorella sp.USTB-01 with the phylogenetic analysis based on 18S ribosomal ribonucleic acid(rRNA)gene sequences.In the heterotrophic batch culture,more than 20.0 g·L^(-1)of cell dry weight concentration(DWC)of Chlorella sp.USTB-01 was obtained at day 5,and which was used directly to seed the autotrophic culture.A novel fermentor-helical combined photobioreactor was established and used to cultivate Chlorella sp.USTB-01 for the fixation of carbon dioxide(CO_(2)).It showed that the autotrophic growth of Chlorella sp.USTB-01 in the combined photobioreactor was more effective than that in the fermentor alone and the maximum DWC of 2.5 g·L^(-1)was obtained at day 6.The highest CO_(2)fixation of 95%appeared on day 1 in the exponential growth phases of Chlorella sp.USTB-01 and 49.8%protein was found in the harvested microalgal cells.
