Koirala Amrit, Alshibli Nabilah Ali, Das Bikram K, Brözel Volker S
Department of Biology and Microbiology, South Dakota State University, Brookings, SD 57007, USA.
Department of Biochemistry, Genetics and Microbiology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria 0028, South Africa.
Microorganisms. 2025 Jan 6;13(1):96. doi: 10.3390/microorganisms13010096.
Nitrogen inputs for sustainable crop production for a growing population require the enhancement of biological nitrogen fixation. Efforts to increase biological nitrogen fixation include bioprospecting for more effective nitrogen-fixing bacteria. As bacterial nitrogenases are extremely sensitive to oxygen, most primary isolation methods rely on the use of semisolid agar or broth to limit oxygen exposure. Without physical separation, only the most competitive strains are obtained. The distance between strains provided by plating on solid media in reduced oxygen environments has been found to increase the diversity of culturable potential diazotrophic bacteria. To obtain diverse nitrogen-fixing isolates from natural grasslands, we plated soil suspensions from 27 samples onto solid nitrogen-free agar and incubated them under atmospheric and oxygen-reducing conditions. Putative nitrogen fixers were confirmed by subculturing in liquid nitrogen-free media and PCR amplification of the genes. Streaking of the 432 isolates on nitrogen-rich R2A revealed many cocultures. In most cases, only one community member then grew on NFA, indicating the coexistence of nonfixers in coculture with fixers when growing under nitrogen-limited conditions. To exclude isolates able to scavenge residual nitrogen, such as that from vitamins, we used a stringent nitrogen-free medium containing only 6.42 μmol/L total nitrogen and recultured them in a nitrogen-depleted atmosphere. Surprisingly, PCR amplification of using various primer pairs yielded amplicons from only 17% of the 442 isolates. The majority of the PCR-negative isolates were and . It is unclear whether these isolates have highly effective uptake systems or nitrogen reduction systems that are not closely aligned with known nitrogenase families. We advise caution in determining the nitrogen fixation ability of plants from growth on nitrogen-free media, even where the total nitrogen is very limited.
为不断增长的人口实现可持续作物生产的氮输入需要增强生物固氮作用。增加生物固氮的努力包括对更有效的固氮细菌进行生物勘探。由于细菌固氮酶对氧气极其敏感,大多数初级分离方法依赖于使用半固体琼脂或肉汤来限制氧气暴露。如果没有物理分离,只能获得最具竞争力的菌株。已发现,在低氧环境下在固体培养基上平板接种所提供的菌株间距离会增加可培养潜在固氮细菌的多样性。为了从天然草地获得多样的固氮分离株,我们将来自27个样本的土壤悬浮液接种到无氮固体琼脂上,并在大气和低氧条件下培养。通过在无氮液体培养基中继代培养和对基因进行PCR扩增来确认推定的固氮菌。在富含氮的R2A上对432个分离株进行划线培养,发现了许多共培养物。在大多数情况下,然后只有一个群落成员能在无氮琼脂上生长,这表明在氮限制条件下生长时,非固氮菌与固氮菌在共培养中并存。为了排除能够清除残留氮(如来自维生素的氮)的分离株,我们使用了一种仅含6.42 μmol/L总氮的严格无氮培养基,并在贫氮气氛中对它们进行再培养。令人惊讶的是,使用各种引物对进行的PCR扩增仅从442个分离株中的17%产生了扩增子。大多数PCR阴性分离株为 和 。目前尚不清楚这些分离株是否具有与已知固氮酶家族不太一致的高效摄取系统或氮还原系统。我们建议在根据植物在无氮培养基上的生长情况来确定其固氮能力时要谨慎,即使总氮含量非常有限。