农业科学与技术:英文版
農業科學與技術:英文版
농업과학여기술:영문판
Agricultural Science & Technology
2012年
10期
2080-2083,2087
,共5页
陈金全%郑燕平%姜丽晶%王风平
陳金全%鄭燕平%薑麗晶%王風平
진금전%정연평%강려정%왕풍평
神珠江口沉积物%氨氧化%amoA基因%Q-PCR
神珠江口沉積物%氨氧化%amoA基因%Q-PCR
신주강구침적물%안양화%amoA기인%Q-PCR
Pearl River Estuary sediment%Ammonia oxidation%amoA gene%Q-PCR
[目的]对珠江口海岸带沉积物中的氨氧化细菌和古菌的组成进行分析,并进行定量研究。[方法]用构建克隆文库和Q-PCR定量的方法对珠江口沉积物中氨氧化细菌和古菌amoA基因的含量和多样性特征进行研究。[结果]在2个沉积物表层,氨氧化古菌的含量是细菌的9和22倍,揭示氨氧化古菌在珠江口的氨氧化过程中起主导作用;系统发育分析表明大多数古菌和细菌的amoA基因序列与不可培养的源于河口区和污染区域的环境克隆子序列有较高的同源性;细菌amoA序列可分成5个类群(Cluster A、B、C、D和E),均属于Nitrosomonas类群,其中Cluster A是主要类群(72.1%);古菌amoA序列分析表明来自于表层的序列有52.2%属于"水/沉积物"簇,47.8%属于"土壤/沉积物"簇,而沉积物底层厌氧区,检测到的古菌amoA基因93.3%属于"土壤/沉积物"簇,6.7%属于"水/沉积物"簇,且amoA基因数量略高于表层。[结论]该研究有助于了解珠江口区域氮的循环过程,为氮的富营养化处理提供重要的理论依据。
[目的]對珠江口海岸帶沉積物中的氨氧化細菌和古菌的組成進行分析,併進行定量研究。[方法]用構建剋隆文庫和Q-PCR定量的方法對珠江口沉積物中氨氧化細菌和古菌amoA基因的含量和多樣性特徵進行研究。[結果]在2箇沉積物錶層,氨氧化古菌的含量是細菌的9和22倍,揭示氨氧化古菌在珠江口的氨氧化過程中起主導作用;繫統髮育分析錶明大多數古菌和細菌的amoA基因序列與不可培養的源于河口區和汙染區域的環境剋隆子序列有較高的同源性;細菌amoA序列可分成5箇類群(Cluster A、B、C、D和E),均屬于Nitrosomonas類群,其中Cluster A是主要類群(72.1%);古菌amoA序列分析錶明來自于錶層的序列有52.2%屬于"水/沉積物"簇,47.8%屬于"土壤/沉積物"簇,而沉積物底層厭氧區,檢測到的古菌amoA基因93.3%屬于"土壤/沉積物"簇,6.7%屬于"水/沉積物"簇,且amoA基因數量略高于錶層。[結論]該研究有助于瞭解珠江口區域氮的循環過程,為氮的富營養化處理提供重要的理論依據。
[목적]대주강구해안대침적물중적안양화세균화고균적조성진행분석,병진행정량연구。[방법]용구건극륭문고화Q-PCR정량적방법대주강구침적물중안양화세균화고균amoA기인적함량화다양성특정진행연구。[결과]재2개침적물표층,안양화고균적함량시세균적9화22배,게시안양화고균재주강구적안양화과정중기주도작용;계통발육분석표명대다수고균화세균적amoA기인서렬여불가배양적원우하구구화오염구역적배경극륭자서렬유교고적동원성;세균amoA서렬가분성5개류군(Cluster A、B、C、D화E),균속우Nitrosomonas류군,기중Cluster A시주요류군(72.1%);고균amoA서렬분석표명래자우표층적서렬유52.2%속우"수/침적물"족,47.8%속우"토양/침적물"족,이침적물저층염양구,검측도적고균amoA기인93.3%속우"토양/침적물"족,6.7%속우"수/침적물"족,차amoA기인수량략고우표층。[결론]해연구유조우료해주강구구역담적순배과정,위담적부영양화처리제공중요적이론의거。
[Objective] This study aimed to investigate the abundance and composition of ammonia-oxidizing bacteria and ammonia-oxidizing archaea in Pearl River Estuary sediment.[Method] Firstly,the amoA gene library was constructed;then based on that,the content and diversity of amoA genes of ammonia-oxidizing bacteria and ammonia-oxidizing archaea in Pearl River Estuary sediment were detected by using quantitative real-time polymerase chain reaction(Q-PCR).[Result] The results of Q-PCR presented that ammonia-oxidizing archaea(AOA) were more abundant than ammonia-oxidizing bacteria(AOB) in the top of sediment cores,with ratios of AOA to AOB of 22 and 9 at the two sites.It suggested that ammonia-oxidizing archaea may play more important roles than ammonia-oxidizing bacteria in the process of ammonia oxidation in the Pearl River Estuary sediment.The phylogenetic tree based on amoA gene sequences revealed that the amoA sequences of both AOA and AOB shared high similarity with the clones from uncultured environment.In the top sediment layer at site Q7,AOB amoA-like gene sequences were dominated by Nitrosomonas-like sequence types,which could be classified into five groups(clusters A,B,C,D and E).Cluster A accounted for 72.1% of the library.In the top sediment layer,the AOA amoA gene fell into two groups "water column/sediment" cluster(52.2%) and "soil/sediment" cluster(47.8%).But in the bottom sediment layer of Q7,most of the AOA amoA sequences(93.3%) fell into "soil/sediment" cluster,and a little part(6.7%) fell into the "water/sediment" cluster.In addition,the total amount of amoA genes in the bottom sediment was higher than that in top sediment.[Conclusion] This study helps to realize the cycle of nitrogen in Pearl River Estuary Region,and thus to provide theoretical support for the treatment of nitrogen eutrophication.