Hoagland Robert E, Boyette Clyde Douglas
Crop Production Systems Research Unit, Department of Agriculture-Agricultural Research Service, Stoneville, MS 38776, USA.
Biological Control of Pests Research Unit, Department of Agriculture-Agricultural Research Service, Stoneville, MS 38776, USA.
J Fungi (Basel). 2021 Nov 30;7(12):1032. doi: 10.3390/jof7121032.
Certain plant pathogens have demonstrated potential for use as bioherbicides for weed control, and numerous studies have been published on this subject for several decades. One of the early examples of an important fungal bioherbicide is , isolated from the weed sicklepod (). To gain further insight into biochemical interactions of this fungus and its host weed, we examined the effects of this bioherbicide on various enzymes associated with plant defense. Young sicklepod seedlings were challenged with spore inoculum and enzyme activities associated with plant defense (peroxidase, proteolytic, and pectinolytic) were assayed periodically over a 96-h time course on plants grown in continuous darkness or continuous light. Peroxidase activity increased with time in untreated control seedlings in both light and dark, but the effect was greater in the light. In -treated plants, peroxidase was elevated above that in control tissue at all sample times resulting in a 1.5 -fold increase above control in light-grown tissue and a 2- to 3-fold increase in dark-grown tissue over 48-96 h. Differences in leucine aminopeptidase activity in control versus -treated tissues were not significant until 48-96 h, when activity was inhibited in fungus-treated tissues by about 32% in light-grown tissue and 27% in dark-grown tissue after 96 h. Proteolytic activity on benzoyl-arginine--nitroanilide was not significantly different in treated versus control tissue in either light or dark over the time course. Pectinase activity increased in treated tissues at all time points as early as 16 h after spore application in light- or dark-grown plants. The greatest increases were 1.5-fold above control levels in light-grown plants (40-64 h) and 2-fold in plants grown in darkness (72-96 h). Data suggests that peroxidase may be involved as defense mechanism of sicklepod when challenged by and that this mechanism is operative in young seedlings under both light and dark growth conditions. Differential proteolytic activity responses on these two substrates suggests the presence of two different enzymes. Increased pectinase activity during pathogenesis suggests that -sicklepod interaction results in an infectivity mechanism to degrade pectic polymers important to sicklepod cell wall integrity. These studies provide important information on some biochemical interactions that may be useful for improvements to biological weed control programs utilizing plant pathogens. Such information may also be useful in genetic selection and manipulation of pathogens for weed control.
某些植物病原体已显示出用作生物除草剂来控制杂草的潜力,几十年来已有众多关于该主题的研究发表。一种重要的真菌生物除草剂的早期例子是从杂草镰荚苜蓿()中分离出来的 。为了进一步深入了解这种真菌与其寄主杂草之间的生化相互作用,我们研究了这种生物除草剂对与植物防御相关的各种酶的影响。用 孢子接种物挑战幼小的镰荚苜蓿幼苗,并在96小时的时间过程中,定期测定在持续黑暗或持续光照下生长的植物中与植物防御相关的酶活性(过氧化物酶、蛋白水解酶和果胶水解酶)。在未处理的对照幼苗中,过氧化物酶活性在光照和黑暗条件下均随时间增加,但在光照条件下效果更明显。在 处理的植物中,在所有采样时间过氧化物酶均高于对照组织,在48 - 96小时内,光照下生长的组织比对照增加了1.5倍,黑暗中生长的组织比对照增加了2至3倍。对照组织与 处理组织中亮氨酸氨肽酶活性的差异直到48 - 96小时才显著,此时在真菌处理的组织中,96小时后光照下生长的组织活性被抑制约32%,黑暗中生长的组织活性被抑制约27%。在整个时间过程中,无论是光照还是黑暗条件下,对苯甲酰 - 精氨酸 - 硝基苯胺的蛋白水解活性在处理组织与对照组织之间均无显著差异。在孢子接种后最早16小时,果胶酶活性在光照或黑暗中生长的处理组织的所有时间点均增加。光照下生长的植物中最大增加量比对照水平高1.5倍(40 - 64小时),黑暗中生长的植物中最大增加量比对照水平高2倍(72 - 96小时)。数据表明,当受到 挑战时,过氧化物酶可能作为镰荚苜蓿的防御机制参与其中,并且这种机制在光照和黑暗生长条件下的幼苗中均起作用。对这两种底物的不同蛋白水解活性反应表明存在两种不同的酶。发病过程中果胶酶活性的增加表明 与镰荚苜蓿的相互作用导致了一种感染机制,以降解对镰荚苜蓿细胞壁完整性很重要的果胶聚合物。这些研究提供了一些生化相互作用的重要信息,这可能有助于改进利用植物病原体的生物杂草控制计划。此类信息也可能有助于杂草控制病原体的遗传选择和操纵。