Wenger K, Bigler L, Suter M J-F, Schönenberger R, Gupta S K, Schulin R
Department of Microbiology, Cornell University, Wing Hall, Ithaca, NY 14853, USA.
J Environ Qual. 2005 Nov 7;34(6):2187-96. doi: 10.2134/jeq2004.0409. Print 2005 Nov-Dec.
DIMBOA (3,4-dihydro-2,4-dihydroxy-7-methoxy-2H-1,4-benzoxazin-3-one), a major benzoxazinone of Poaceae plants, was isolated and purified from corn seedlings. The effect of isolated and purified DIMBOA on the degradation of atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine], and its toxic breakdown products, desethylatrazine [2-chloro-4-amino-6-(isopropylamino)-s-triazine; DEA] and desisopropylatrazine [2-chloro-4-(ethylamino)-6-amino-s-triazine; DIA], was studied in the absence of plants using batch experiments, while the effect of corn root exudates on these compounds was determined in hydroponic experiments. Degradation experiments were performed in the presence and absence of 50 microM, 1 mM, or 5 mM DIMBOA resulting in ratios of DIMBOA to pesticide of 1:1, 20:1, and 100:1. We observed a 100% degradation of atrazine to hydroxyatrazine within 48 h at a ratio of DIMBOA to atrazine of 100:1. DIMBOA had the largest effect on atrazine, while it was about three times less effective on DEA and DIA. Corn (Zea mays L. cv. LG 2185) was exposed to 10 mg L(-1) of either atrazine, DEA, or DIA for 11 d in a growth chamber experiment. Up to 4.3 micromol L(-1) d(-1) of hydroxyatrazine were formed in the nutrient solutions by plants exposed to atrazine, while the formation of hydroxylated metabolites from plants exposed to DEA and DIA was smaller and also delayed. The formation of hydroxylated metabolites increased in the solution with plant age in all atrazine, DEA, and DIA treatments. HMBOA (3,4-dihydro-2-hydroxy-7-methoxy-2H-1,4-benzoxazin-3-one), the lactam precursor of DIMBOA, and a tentatively identified derivative of MBOA (2,3-dihydro-6-methoxy-benzoxazol-2-one) were detected in the corn root exudates. Mass balance calculations revealed that up to 30% of the disappearance of atrazine and DEA, and up to 10% of DIA removal from the solution medium in our study could be explained by the formation of hydroxylated metabolites in the solution itself. Our results show that higher plants such as corn have the potential to promote the hydrolysis of triazine residues in soils by exudation of benzoxazinones.
3,4-二羟基-7-甲氧基-2H-1,4-苯并恶嗪-3-酮(DIMBOA)是禾本科植物中的一种主要苯并恶嗪酮,从玉米幼苗中分离并纯化得到。在无植物存在的情况下,通过批次实验研究了分离纯化的DIMBOA对莠去津[2-氯-4-(乙氨基)-6-(异丙氨基)-均三嗪]及其有毒降解产物去乙基莠去津[2-氯-4-氨基-6-(异丙氨基)-均三嗪;DEA]和去异丙基莠去津[2-氯-4-(乙氨基)-6-氨基-均三嗪;DIA]降解的影响,同时在水培实验中测定了玉米根系分泌物对这些化合物的影响。在有和没有50微摩尔/升、1毫摩尔/升或5毫摩尔/升DIMBOA存在的情况下进行降解实验,得到的DIMBOA与农药的比例分别为1:1、20:1和100:1。我们观察到,在DIMBOA与莠去津比例为100:1时,48小时内莠去津100%降解为羟基莠去津。DIMBOA对莠去津的影响最大,而对DEA和DIA的影响约为其三分之一。在生长室实验中,将玉米(Zea mays L. cv. LG 2185)暴露于10毫克/升的莠去津、DEA或DIA中11天。暴露于莠去津的植物在营养液中形成的羟基莠去津高达4.3微摩尔/升·天,而暴露于DEA和DIA的植物形成的羟基化代谢产物较少且延迟。在所有莠去津、DEA和DIA处理中,随着植物生长,溶液中羟基化代谢产物的形成增加。在玉米根系分泌物中检测到了HMBOA(3,4-二氢-2-羟基-7-甲氧基-2H-1,4-苯并恶嗪-3-酮),即DIMBOA的内酰胺前体,以及一种初步鉴定的MBOA(2,3-二氢-6-甲氧基-苯并恶唑-2-酮)衍生物。质量平衡计算表明,在我们的研究中,溶液介质中莠去津和DEA消失量的30%以及DIA去除量的10%可归因于溶液本身中羟基化代谢产物的形成。我们的结果表明,像玉米这样的高等植物有可能通过分泌苯并恶嗪酮促进土壤中三嗪类残留物的水解。