连香树人工林根系分泌物输入季节性变化及其驱动的根际微生物特性研究

根系分泌物介导的根际过程具有重要的生态学效应,但目前有关植物尤其是濒危珍稀植物根系分泌物及其介导的土壤生物地球化学循环过程的原位季节动态研究甚少。本文以阿坝州茂县大沟流域30年生的国家二级濒危保护植物连香树人工林为研究对象,于2014年4、7、9和12月利用原位收集装置对连香树根系分泌物进行原位收集;并同步分析了根际土壤微生物特性的变化。结果表明：（1）根系分泌物C和N分泌速率均呈现明显的季节动态变化,其中,夏季最高,冬季最低。（2）根际土壤微生物碳、氮及土壤酶活性显著高于非根际,表现出正的根际效应;根际效应也与根系分泌物输入表现出类似的季节动态规律,即夏季（7月）最高,而冬季（12月）最低。（3）进一步相关分析表明：根系分泌物分泌速率与土壤微生物碳、氮及土壤酶活性根际效应值呈线性正相关,表明根系分泌物输入是驱动根际微生物活性的重要因子,揭示连香树根系碳输入对根际土壤过程和功能的季节响应。未来研究应加强根系分泌物输入与土壤生物地球化学循环过程的偶联效应与机制研究。     

Influence of Celery on the Remediation of PAHs-contaminated Farm Soil

Polycyclic aromatic hydrocarbons (PAHs) contamination has been considered as one of the major environmental concerns for farmland soil all over the world including China. Due to small per capita land area, to find crops or vegetable, which could not only degrade the PAHs contaminants but also would not concentrate PAHs, was particularly important. Celery was selected as the phytoremediator in this experiment, and the soil enzyme activity, PAHs-degrading microorganisms, and the speciation of PAHs in soil were studied. The results showed that celery could significantly enhance the remediation of PAHs compared with the controlled experiment after 90 days (p< 0.01), and the removal efficiency were 31.29%, 30.79%, and 50.21% in the soil, non-rhizosphere soil, and rhizosphere soil, respectively. The soil enzyme activity and PAHs-degrading microorganisms significantly increased in rhizosphere soil compared with non-rhizosphere soil (p< 0.05), and the bioaccessibility of PAHs in soil could have been enhanced in the presence of celery root exudates. Those would help the bioremediation of PAHs by soil microorganisms. Meanwhile, the concentration of PAHs in the edible portion of celery was only 17.13 ± 1.24 μg/kg, and the bioconcentration factors in the aboveground part of celery were only 0.025. This study provides a potential in-site farmland soil phytoremediation technology that could have practical utility.     

The degradation of arsenobetaine to inorganic arsenic by sedimentary microorganisms

Two growth media containing arsenobetaine [(CH₃)₃ As⁺ CH₂COO^–] were mixed with coastal marine sediments, the latter providing a source of microorganisms. The mixtures were kept at 25 °C in the dark and shaken for several weeks under an atmosphere of air. The disappearance of arsenobetaine and the appearance of two metabolites were followed by HPLC. The HPLC-retention time of the first metabolite agreed with that of trimethylarsine oxide [(CH₃)₃AsO]. The second metabolite was identified as arsenate (As(V)) using hydride generation/cold trap/GC MS analysis and thin layer chromatography. This is the first scientific evidence showing that arsenobetaine is degraded by microorganisms to inorganic arsenic via trimethylarsine oxide. The degradation of arsenobetaine to inorganic arsenic completes the marine arsenic cycle that begins with the methylation of inorganic arsenic on the way to arsenobetaine.     

大麦虫及其肠道微生物对聚乙烯的生物降解

【背景】废旧塑料聚乙烯因具有较高的化学惰性,不易被自然降解而形成长期污染。【目的】探究聚乙烯泡沫塑料对大麦虫生长发育的影响,为大麦虫作为降解聚乙烯泡沫塑料的昆虫推广提供理论依据。【方法】以大麦虫幼虫为研究对象,选用常见的泡沫塑料(聚乙烯),采用4种不同的饲喂方式T1 (麦麸)、T2 (泡沫塑料)、T3 (泡沫塑料+麦麸)、T4 (不饲喂)进行驯化,处理30 d后对大麦虫进行解剖,取肠道内容物于LB培养基中进行富集培养,将富集培养后的菌液加入以聚乙烯(polyethylene,PE)为唯一碳源的LCFBM培养基进行选择性培养,从中筛选分离得到对PE塑料有降解能力的菌株。【结果】取食泡沫塑料30d后,与单一饲喂PE相比,麦麸和PE混合饲喂后大麦虫幼虫的存活率为76%。采用傅里叶变换红外光谱检测发现虫粪组分中主要官能团中峰值明显变化,表明PE长链有断裂现象,并从肠道中分离得到3株可以对PE薄膜边缘造成明显侵蚀的菌株。【结论】大麦虫可取食并消化PE塑料,其肠道内的微生物对PE塑料的降解起到关键作用,研究结果为塑料污染的生物降解提供了科学证据。     

微生物在镉污染土壤修复中的应用及其作用机理

土壤中镉（Cd）含量的超标导致了土壤生态系统的恶性发展,微生物作为土壤中的常见组分之一在缓解土壤镉污染中展现出巨大潜力。本文总结了微生物、微生物-植物和微生物-生物炭在镉污染土壤修复中的应用并阐述了相关的作用机理。芽孢杆菌（Bacillus）、不动杆菌（Acinetobacter）、荧光假单胞菌（Pseudomonas fluorescence）、丛枝菌根真菌（arbuscular mycorrhizal fungi,AMF）等微生物可以通过吸附、矿化、沉淀、溶解等方式改变镉的生物有效性,从而达到缓解镉污染的目的。pH值、温度、微生物生物量、镉初始浓度以及时间等对微生物降低镉的生物有效性方面有着显著的影响。假单胞菌、伯克霍尔德菌（Burkholderia）、黄杆菌（flavobacterium）等微生物可以通过促生、活化等作用促进超富集植物对Cd²⁺的吸收。生物炭作为一种土壤改良剂,其独有的理化性质可以作为微生物的庇护所。微生物-生物炭联合使用与单用生物炭相比可以进一步促进镉的残渣态的增加,降低土壤中有效态的比例。     

撕裂蜡孔菌HG2011对光叶紫花苕结瘤固氮的影响及其潜在机制

【目的】 在我国南方尤其是西南地区,光叶紫花苕(Vicia villosa Roth.)作为重要的青饲和绿肥两用豆科作物被广泛种植,有助于提高土壤氮素和后茬作物的产量品质。接种有益微生物是促进豆科作物生物固氮和生长的重要措施之一。为此,本文研究了一株自主分离获得的白腐真菌¾¾撕裂蜡孔菌(Careporia lacerata HG2011)对光叶紫花苕结瘤固氮和生长的影响,并揭示其潜在机制。【方法】 采用微生物培养、植物培养和田间试验,研究C. lacerata磷铁活化能力、代谢产物构成、与根瘤菌Rhizobium sophorae S3的相互作用,及其对光叶紫花苕结瘤、生长、产量、品质和土壤有效磷铁的影响。【结果】 C. lacerata和根瘤菌之间无拮抗作用。液相色谱-质谱(liquid chromatography-mass spectrometry, LC-MS)分析发现,C. lacerata发酵液含有氨基酸、有机酸和类黄酮等化感物质,能增强根瘤菌的趋化性并促进生物膜形成。此外,C. lacerata还能释放生长素、赤霉素、水杨酸和铁载体,活化难溶性有机和无机磷。在植物培养试验中,单独接种C. lacerata或根瘤菌均能促进光叶紫花苕生长,但以共接种处理效果最佳。C. lacerata定殖于光叶紫花苕根际,导致根长、根系表面积和结瘤数显著增加。田间试验发现,接种C. lacerata显著提高了光叶紫花苕单株根瘤数、根瘤质量和固氮酶活性,以及土壤有效磷铁含量和磷酸酶活性,产量比常规施肥处理增加12.15%且品质无显著变化。【结论】 C. lacerata能够在光叶紫花苕根际定殖,通过分泌化感物质、生长素和活化土壤磷铁等机制促进结瘤固氮和生长发育。C. lacerata易于培养,菌剂制备成本低廉,施用简便,对提高豆科作物产量品质具有一定应用价值。     

Carbon sink reduction by fruit removal triggers respiration but not nitrous oxide emissions from the root zone of cucumber

Root exudation of organic carbon (C) is generally believed to be the cause of positive effects of root activity on nitrous oxide (N₂O) emissions. We tested the effects of root exudation in an actual soil–plant system on N₂O emissions while excluding most other potential factors. The C source/sink ratio in cucumber was changed by removing fruits to increase root exudation. Root‐zone emissions of carbon dioxide (CO₂) and N₂O were monitored in complete stands of adult plants in a greenhouse. Whereas CO₂ emissions rapidly increased as a result of fruit removal the N₂O emissions were completely unaffected. After cutting the shoots CO₂ emissions decreased within 2 weeks in both the fruit removal treatment and the control to a value significantly lower than that before the start of the treatments. However, N₂O emissions immediately exhibited a short peak, which was significantly higher in the fruit removal treatment compared to the control. Thereafter N₂O emissions in both treatments remained on the same level but considerably higher than before shoot cutting. We concluded that in a well‐aerated root zone, a root exudation pulse does not necessarily increase N₂O emissions, because C substrates are quickly respired by microorganisms before they can support heterotrophic denitrification. The results further indicate the significance of dying/dead roots for the creation of denitrificaton hot‐spots, which likely result from providing C substrates as well as poorly aerated habitats.     

Seed coating with beneficial microorganisms for precision agriculture

Seed coating is a technique of covering seeds with adhesive agents to improve seed performance and plant establishment while reducing production cost. To meet the needs of development of precision agriculture, seed coating has been widely used in agriculture as an effective means to alleviate biotic and abiotic stresses, thus enhancing crop growth, yield, and health. Plant growth promoting microorganisms (PGPM) are recognized as essential contributors to improving agricultural productivity via direct application to the rhizosphere and plant tissues, or seed inoculation. However, during conventional inoculation processes, several factors such as insufficient microbial survival, hindrance in the application of biocontrol inocula to the seeds and exposure to unsuitable temperature and light in subsequent seed storage, force us to explore efficient and reliable microbial application tools. Recently, biological seed coating with PGPM is proposed as an alternative to conventional seed treatment (such as fertilizer and protection products) due to its ecological safety and socio-economic aspects. In this review, microbial seed coating technology and its contribution to sustainable precision agriculture are well discussed and highlighted in the extensive table and elaborate schematic drawings.     

Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part I: processes with isolated enzymes

Traditional cultivation-based methods to quantify microbial abundance are not suitable for analyses of microbial communities in environmental or medical samples, which consist mainly of uncultured microorganisms. Recently, different cultivation-independent quantification approaches have been developed to overcome this problem. Some of these techniques use specific fluorescence markers, for example ribosomal ribonucleic acid targeted oligonucleotide probes, to label the respective target organisms. Subsequently, the detected cells are visualized by fluorescence microscopy and are quantified by direct visual cell counting or by digital image analysis. This article provides an overview of these methods and some of their applications with emphasis on (semi-)automated image analysis solutions.