铜绿微囊藻在不同供磷水平下对砷胁迫的响应

龚艳, 吴幸强, 肖邦定, 方涛, 刘剑彤, 宋立荣

龚艳, 吴幸强, 肖邦定, 方涛, 刘剑彤, 宋立荣. 铜绿微囊藻在不同供磷水平下对砷胁迫的响应[J]. 水生生物学报, 2009, 33(5): 890-895.
引用本文: 龚艳, 吴幸强, 肖邦定, 方涛, 刘剑彤, 宋立荣. 铜绿微囊藻在不同供磷水平下对砷胁迫的响应[J]. 水生生物学报, 2009, 33(5): 890-895.
GONG Yan, WU Xing-Qiang, XIAO Bang-Ding, FANG Tao, LIU Jian-Tong, SONG Li-Rong. RESPONSE OFM ICROCYSTIS AERUG INOSA TO ARSENATE UNDER D IFFERENT PHOSPHATE REGIMES[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(5): 890-895.
Citation: GONG Yan, WU Xing-Qiang, XIAO Bang-Ding, FANG Tao, LIU Jian-Tong, SONG Li-Rong. RESPONSE OFM ICROCYSTIS AERUG INOSA TO ARSENATE UNDER D IFFERENT PHOSPHATE REGIMES[J]. ACTA HYDROBIOLOGICA SINICA, 2009, 33(5): 890-895.

铜绿微囊藻在不同供磷水平下对砷胁迫的响应

基金项目: 

国家973项目(2002CB42300)资助

RESPONSE OFM ICROCYSTIS AERUG INOSA TO ARSENATE UNDER D IFFERENT PHOSPHATE REGIMES

  • 摘要: 采用磷饥饿培养后的微囊藻细胞进行不同供磷水平的五价砷(As(V))暴露实验,考察单一胞外磷变化的情况下As(V)对滇池分离出的铜绿微囊藻FACHB905生长及产毒的影响。结果表明胞外磷浓度变化不会影响铜绿微囊藻对As(V)的耐受阈值(-0-7mol/L)。少磷条件下的半数抑制浓度(IC50)为0-2.79mol/L,比无磷条件下的IC50(0-5.8mol/L)高3个数量级,并且少磷条件下As(V)与细胞活性位点的结合常数要远低于无磷条件,因此胞外磷在As(V)对微囊藻的毒性效应上具有关键的作用。As(V)对微囊藻单细胞的叶绿素含量没有显著影响,但是对毒素产量具有剂量效应。在少磷条件下,As(V)浓度大于0-7mol/L可促进微囊藻FACHB905的胞内产毒量;而在无磷条件下,所有As(V)处理组的胞内产毒量均上升78%左右。由上可知,微囊藻在产毒方面与As(V)具有协同效应,这对于全面了解滇池水华暴发期间毒素的变化规律具有一定的参考价值。
    Abstract: Arsenic is ubiquitous in the environment and potentially toxic to humans. Arsenate,thermodynamically theominant specie of arsenic in marine and estuarine surface waters,was shown to be taken up by the phosphate transportystems of phytop lankton and plants due to its similar structure to the phosphate. Considerable evidence has been foundhatMicrocystis luxuriously up take phosphate toform polyphosphate bodies in phosphate-rich environments. The cyanobac-erial sensitivity to arsenate has often been linked to the structural similarities of arsenate and phosphate,and intracellularolyphosphate was shown to be related to the sensitivity to arsenate. Therefore,the present research was intended to ex-lore the effects of arsenate on the growth and microcystin production ofMicrocystis aeruginosa FACHB905,which isolatedrom Dianchi Lake when only the extracellular phosphate concentration was changeable. The cells of M. aeruginosaACHB905 were cultivated in the phosphate-free BG-11 medium for 14 days in order to completely consume phosphatetored in the cyanobacterial cells. Then,these phosphate-starved cellswere inoculated in modified BG-11 media adjusteds following two cases: PO3 - was added at 1μM for the phosphate-limited medium,and PO3 - was absent as the phosphate-eprived medium. Arsenate as Na-HAsO4 was added to the culture media at concentrations from 10 - 8 to 10 - 4M. It wasorthwhile mentioning that the phosphate concentration used in this study (1μmol/L) was similar to that under naturalonditions. We measured the density of cultures,chlorophyll content and microcystin content of this cyanobacterium re-ponding to arsenate under both the phosphate regimes. This study showed that the extracellular phosphate concentrationad no reference to the threshold doses (- 10-7mol/L) ofM. aeruginosa FACHB905 to arsenate. However,the IC50 val-e under phosphate limitation was 10--.79mol/L and three magnitudes greater than that under phosphate deprivation. Thepparent association constant of arsenate to the cyanobacterium under phosphate limitation wasmuch lower than that underhosphate deprivation. Thus,it presumed that extracellular phosphate had the key role on protecting cyanobacterial cellsrom arsenate. Otherwise,arsenate did not affect the chlorophyll content per cell,but had dosage effect on the cellularmi-rocystin content. Arsenate,higher than 10-7mol/L,could promote the cellularmicrocystin content per cell under phos-hate limitation,while the microcystin content of all arsenate treatments was stimulated about 78% of that of the controlnder phosphate deprivation. The synergistic effect of arsenate and microcystin production ofM. aeruginosa FACHB905 isf definite significance for complete understanding the microcystin production in the blooms in Dianchi Lake.
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出版历程
  • 收稿日期:  2008-01-10
  • 修回日期:  2008-10-28
  • 发布日期:  2009-09-24

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