Accelerating carbon conversion in garden waste composting with food waste-expanding microbial inoculants
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摘要: 高木质纤维素含量制约了园林废弃物的堆肥化应用, 添加外源菌剂是加快木质纤维素降解的有效手段。为降低菌剂生产成本并提高接种效率, 本研究利用食品残渣(苹果渣、豆渣)代替常规碳氮源(葡萄糖、蛋白胨)进行木质纤维素降解菌的扩繁, 扩繁产品活菌数高达3.7×1010 cfu∙mL−1, 相较工业培养基增加46.2%。进一步探讨了不同降解菌接种量(0、2%、4%、8%, 干重计)对园林废弃物堆肥过程碳素转化的影响。结果表明, 接种处理显著增加了木质纤维素的降解(P<0.05), 2%、4%和8%接种处理(2%IM、4%IM、8%IM)的总木质纤维素降解率较CK分别提高6.3%、9.2%和23.0%; 其中8%IM处理加速了碳素的完全矿化, 导致腐殖质前体物(多酚、还原糖)被完全降解生成CO2, 抑制了腐殖化的进行; 而4%IM处理在加快木质纤维素降解的同时促进了腐殖酸(HA)的合成, 其最终HA含量达91.3 g∙kg−1, 较CK、2%IM和8%IM处理分别提高24.9%、10.7%和35.8%。因此, 以食品残渣为培养基质可完全实现木质纤维素降解菌的生长扩繁, 同时, 4%接种量更有利于园林废弃物堆肥腐殖化的进行和碳素的保存, 本研究为多源废弃物高效协同处理提供了理论依据。Abstract: The expansion of urbanization has resulted in the generation of a large amount of garden waste (40 million tons per year in China), while traditional treatment methods (incineration and landfill) tend to cause serious environmental pollution and waste of resources. Composting is an effective way to realize resource utilization of garden waste. However, the high lignocellulose content of garden waste limits its resource utilization. Accelerating the degradation of lignocellulose in the composting process is of great significance for achieving effective resource utilization of garden waste. Inoculation with exogenous microorganisms is considered an environmentally friendly and cost-effective method to accelerate lignocellulose degradation, which would further reduce the cost of inoculum production and improve inoculation efficiency. In this study, food residues (apple pomace and bean dregs) were used instead of conventional carbon and nitrogen sources (glucose and peptone) to propagate lignocellulose-degrading fungi. The number of viable fungi in the multiplication product reached 3.7×1010 cfu∙mL−1, which increased by 46.2% compared with the traditional industrial medium. The effects of different inoculum amounts (0, 2%, 4%, and 8%, dry weight) on carbon conversion during garden waste composting were also discussed. The inoculation treatments significantly increased lignocellulose degradation (P<0.05), according to the results. The total lignocellulose degradation rates of the 2%, 4%, and 8% inoculation treatments (2%IM, 4%IM, and 8%IM) increased by 6.3%, 9.2%, and 23.0%, respectively, compared with CK. Dynamic changes in humus precursors (reducing sugars and polyphenols) and humus components were further analyzed. The 8%IM treatment accelerated the complete mineralization of carbon, resulting in the complete degradation of the humus precursors (polyphenols and reducing sugars) into CO2, which inhibited humification. Compared with CK, 2%IM, and 4%IM, the cumulative CO2 emissions of 8%IM increased by 21.9%, 22.3%, and 26.0%, respectively. The 4%IM treatment accelerated lignocellulose degradation while promoting the synthesis of humic acid (HA). The final HA content reached 91.3 g∙kg−1, which was 24.9%, 10.7%, and 35.8% higher than that of CK, 2%IM, and 8%IM treatments, respectively. These results indicate that appropriate inoculation is beneficial to the directional transformation of lignocellulose to humic acid, whereas excessive inoculation would lead to an excessive loss of organic matter due to the high metabolic activity of microorganisms; and the degradation efficiency of lignocellulose is lower when inoculated with a small amount, which was further confirmed by the partial least squares path analysis model in this study. The conversion of lignocellulose to dissolved organic carbon increased with increasing inoculation amount (correlation coefficients of CK, 2%IM, 4%IM, and 8%IM were 0.59, 0.70, 0.75, and 0.85, respectively), while the correlation coefficient of 4%IM from DOC to HA was −0.85, which was higher than 2%IM (−0.76) and 8%IM (−0.34). Therefore, the growth and propagation of lignocellulose-degrading fungi can be completely realized by using food residues as a culture substrate. A 4% inoculation amount was more conducive to the humification of garden waste compost and the preservation of carbon. This study provides a reference for the garden waste composting inoculation process and a theoretical basis for multi-source waste-efficient collaborative treatment.
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Key words:
- Composting /
- Garden waste /
- Carbon transformation /
- Food waste /
- Lignocellulose degradation /
- Humification
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图 1 接种量对堆肥过程木质纤维素降解的影响
CK: 对照; 2%IM: 添加2%菌剂; 4%IM: 添加4%菌剂; 8%IM: 添加8%菌剂; 不同小写字母表示不同处理间存在显著性差异(P<0.05)。CK: control; 2%IM: adding 2% microbial inoculum; 4%IM: adding 4% microbial inoculum; 8%IM: adding 8% microbial inoculum. Different lowercase letters indicate significant differences among different treatments (P<0.05)
Figure 1. Effects of inoculum size on lignocellulose degradation during composting
图 5 接种量对堆肥碳素转化途径的影响
DOC: 可溶性有机碳; Lce: 木质纤维素; HA: 腐殖酸。CK: 对照; 2%IM: 添加2%菌剂; 4%IM: 添加4%菌剂; 8%IM: 添加8%菌剂。DOC: dissolved organic carbon; Lce: lignocellulose; HA: humic acid. CK: control; 2%IM: adding 2% microbial inoculum; 4%IM: adding 4% microbial inoculum; 8%IM: adding 8% microbial inoculum.
Figure 5. Effects of inoculum size on carbon conversion pathway during composting
表 1 试验材料的理化性状
Table 1. Physical and chemical properties of the experimental materials
试验材料
Material含水率
Moisture
content (%)有机质a
Organic
matter (%)总氮a
Total
nitrogen (%)碳氮比a
C/NpH 电导率
Electrical
conductivity (mS·cm−1)总糖a
Total sugar
content (%)园林废弃物
Garden waste11.00±0.34 84.74±0.56 1.49±0.00 34.14±0.20 7.32±0.02 1.55±0.17 — 餐厨垃圾
Food waste78.55±2.23 91.74±0.11 2.89±0.02 14.61±0.32 4.58±0.07 3.30±0.20 — 苹果渣
Apple pomace82.81±0.58 98.04±0.14 0.81±0.02 69.87±1.82 5.67±0.09 — 20.75±0.58 豆渣
Bean dregs79.95±4.14 95.73±0.07 2.64±0.01 21.02±0.09 7.07±0.04 — 37.29±1.29 “a”: 基于物料干重; “—”: 表示未检测。“a”: based on dry weight of material; “—”: not measured. 表 2 食品残渣(苹果渣、豆渣)代替常规碳、氮源(培养基 Ⅱ)对培养72 h后菌液活菌数与酶活性的影响
Table 2. Effect of food residues (apple pomace, soybean dregs) instead of conventional carbon and nitrogen sources (Medium Ⅱ) on the viable count and enzymatic activity of the broth after 72 h incubation
处理
Treatment活菌数
Viable count
(×010 cfu∙mL−1)木聚糖酶
Xylanase
(U∙mL−1)纤维素酶
Cellulase
(U∙mL−1)漆酶
Laccase
(U∙mL−1)锰过氧化物酶
Manganese peroxidase
(U∙mL−1)木质素过氧化物酶
Lignin peroxidase
(U∙mL−1)培养基Ⅰ Medium Ⅰ 2.53±0.41a 337.40±108.81a 73.82±9.55a 3.71±0.69a 11.26±3.97a 2.98±1.67a 培养基Ⅱ Medium Ⅱ 3.70±0.37b 597.40±171.21b 99.47±5.99b 4.91±2.22a 22.38±2.46b 12.39±1.67b 不同小写字母表示不同处理间存在显著性差异(P<0.05)。Different lowercase letters indicate significant differences between two treatments (P<0.05). -
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