机构地区:[1]浙江师范大学化学与生命科学学院,浙江金华321004
出 处:《土壤学报》2020年第6期1483-1491,共9页Acta Pedologica Sinica
基 金:国家自然科学基金项目(41371291);浙江省公益技术应用研究计划项目(LGN20D010002)资助。
摘 要:利用AM真菌(Glomus intraradices)与毛根农杆菌质粒DNA转化的胡萝卜根(Ri T-DNA transformed carrotroots)建立的双重培养系统,以及同位素示踪技术探究AM真菌共生系统中硝态氮NO-3转运吸收途径,对铵态氮和硝态氮吸收合成精氨酸进行研究;并开展农田试验研究铵态氮和硝态氮吸收转运对寄主生长的影响。研究发现AM真菌菌丝在NH+4和NO3-共存时,优先吸收NH+4。当AM真菌的根外菌丝用NH415NO3处理1周时,虽然根外菌丝的自由氨基酸未被15N标记,包括精氨酸,但是菌根组织中的自由氨基酸被15N标记,揭示了15 NO3-沿着菌丝直接转运至菌根组织而不是来自于精氨酸转运的新模式;而根外菌丝用15NH4NO3处理时菌根组织中只有精氨酸被15N标记,而其他氨基酸合成的氮素主要来自菌丝室运转来的14 NO3-,所以未被标记。AM真菌根外菌丝加13C6-葡萄糖,培养6周后,发现菌根组织的精氨酸和蛋白质均未发现13C,说明其根外菌丝不能利用葡萄糖。菌丝室加13C1.2-乙酸钠后,菌根组织的精氨酸和蛋白质均发现13C,分别为8.5%±2.3%和7.6%±0.7%,说明其根外菌丝能吸收利用乙酸盐中的碳素。菌丝室加13C1.2-乙酸钠+15NO3后,随着氮源的增加,其自由精氨酸浓度提高为54.2%±19.3%,菌根蛋白质中精氨酸浓度变化不大;同时菌根组织的精氨酸和蛋白质中C/N同位素标记丰度大大提高,分别为57.4%±4.8%和50.3%±2.8%,说明菌丝室加碳源乙酸和氮源,可以提高精氨酸的合成。大田试验中,在低磷条件下,接种AM真菌并添加硝酸钾后菌根化甜玉米茎叶重明显提高,相比对照的甜玉米提高了12.28%;硫酸铵则不如硝酸钾对AM真菌菌根化甜玉米株重的促进作用,反而是降低了其生物量8.19%,尿素则降低了13.02%,但尿素再加有机肥则可以缓解对生物量的降低作用。【Objective】Effects of uptake and translocation of NO-3 in arbuscular mycorrhizal symbiosis and formation of arginine(Arg)in extraradical mycelium(ERM)and mycorrhizal root when ERM was exposed to NO-3 or NH+4,affecting growth of their host plants were studied.【Method】In this study a dual split culture system was established with Ri T-DNA transformed carrot root and Glomus intraradices(Rhizophagus intraradices)and the 15N/13C isotope tracing technique was used to explore pathways of the uptake and transport of NO-3,and determine how much arginine accumulated in ERM and mycorrhizal root after NO-3 or NH+4 was absorbed and translocated in the fungal compartment,and a field experiment was conducted too to address how uptake and translocatiton of NO-3 or NH+4 affect growth of the host plants.【Result】Results show that AM hypha preferred to uptake NH+4 over NO-3 when they both were available in the soil.When AM extraradical hypha were exposed to NH415NO3 for 1 week,though the free amino acids,include Arg,in the extraradical mycelium(ERM)were not labelled by 15N,those in the mycorrhizal tissues were,indicating that 15NO3 in the fungal compartment were transported directly via mycelium into mycorrhizal tissues rather than any new translocation mode;on the contrary,when extraradical hypha were cultured with 15NH4NO3,only Arg was 15N-labelled therein,while the form of nitrogen composed of other amino acids in the ERM was 14NO3 translocated mainly from the hypha compartment and hence not labelled.While exposed to 13C6-Glucose for 6 weeks,the ERM was found to have no 13C-labelled Arg or protein,which indicates that ERM is unable to utilize glucose.When exposed to 13C1,2-acatate,the ERM was found to have Arg and protein 13C labelled up to 8.5%±2.3%and 7.6%±0.7%,respectively;when exposed to 13C1,2-acatate plus 15 NO3-,the ERM increased the concentration of free Arg with increasing N input,up to 54.2%±19.3%and 13C labelled Arg and protein up to 57.4%±4.8%and 50.3%±2.8%,respectively,which indicates that increased
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...