林业科学 ›› 2026, Vol. 62 ›› Issue (5): 27-39.doi: 10.11707/j.1001-7488.LYKX20250610
收稿日期:2025-10-10
修回日期:2026-03-30
出版日期:2026-05-10
发布日期:2026-05-12
通讯作者:
韦小丽
E-mail:gdwxl2022@163.com
基金资助:
Yan He1,Nianjie Shang1,2,Shicheng Su1,Xiaoli Wei1,*(
)
Received:2025-10-10
Revised:2026-03-30
Online:2026-05-10
Published:2026-05-12
Contact:
Xiaoli Wei
E-mail:gdwxl2022@163.com
摘要:
目的: 探究种子际真菌引发对花榈木种子萌发的生理生化机制,为具有硬实特性的林木种子破除休眠提供理论依据和菌种保障。方法: 从花榈木种子际土壤中分离出3株促萌发真菌,测定其促进种皮分解相关酶的分泌能力及内源激素合成量。利用3株真菌引发花榈木种子进行发芽试验,测定其萌发不同阶段的生理生化指标,并以常规方法处理花榈木种子验证引发效果,系统评估3株种子际真菌对花榈木种子萌发的生理调控效应。结果: 1) 菌株SS-1-14、SS-2-3和SS-2-22在培养7天内均能分泌促进种皮分解相关酶。SS-1-14优先降解果胶层,SS-2-3持续释放高活性果胶酶和脂肪酶,SS-2-22则在初期快速产生纤维素酶和果胶酶,高效瓦解种皮屏障。2) 3株菌株均能分泌生长素和细胞分裂素前体,激活种胚细胞分化。SS-1-14产生的吲哚乙酸、水杨酸以及水杨酸葡萄糖苷含量高,兼具促生长与激活系统抗性功能。SS-2-3产吲哚-3-乙腈、3-(2-氨乙基)吲哚和玉米素较多,直接调控细胞分裂和胚芽分化。SS-2-22以生长素类和细胞分裂素前体(N6-异戊烯基腺苷、异戊烯基腺嘌呤)为主,通过前体物质转化合成活性激素,降低代谢负担。3) 种子际真菌引发是通过动态调控花榈木种子的抗氧化酶和贮藏物质代谢,有效促进种子萌发。3株菌株通过调控整个萌发过程中CAT和PPO、后期POD和SOD增强抗氧化能力。SS-1-14菌株引发对种子酶活性的调控效果最佳,可将种子萌发后期SOD以及前、后期CAT活性显著提高19.10%、127.13%和41.20%。3株菌株通过调控整个萌发过程中蛋白酶、脂酶及后期的淀粉酶、酸性磷酸酶活性促进贮藏物质转化,其中SS-1-14作用最为显著,可将种子萌发前、后期的蛋白酶和脂酶分别提高67.31%、58.61%和77.16%、59.32%。3株菌株均可加速整个萌发过程的大分子物质降解以及小分子物质生成,其中SS-1-14引发综合效果最佳,使种子萌发前期甘油三酯、后期淀粉降解率增加32.20%、60.51%,并使种子萌发前期ATP、后期可溶性糖生成分别加快188.83%、65.24%。4) 与刻伤、酸蚀、热水浸泡等传统物理化学处理方法相比,真菌引发可降低种子电导率以及MDA含量,缓解萌发过程中的氧化损伤,维持细胞膜系统的完整性。结论: 种子际真菌通过分泌促进种皮分解酶破除机械障碍、合成植物激素激活种子生理活性,增强抗氧化酶与物质转化酶系统以降低萌发损伤并促进贮藏物质转化,形成“物理?化学?生物”多维度的引发机制,从而促进花榈木硬实种子的萌发。
中图分类号:
何燕,尚念杰,苏石诚,韦小丽. 种子际真菌引发花榈木种子萌发的生理生化机制[J]. 林业科学, 2026, 62(5): 27-39.
Yan He,Nianjie Shang,Shicheng Su,Xiaoli Wei. Physiological and Biochemical Mechanisms of Spermosphere Fungi Induing Germination of Ormosia henryi Seeds[J]. Scientia Silvae Sinicae, 2026, 62(5): 27-39.
表1
种子际真菌对花榈木种子萌发的影响"
| 菌株 Strain | 发芽率 Germination percentage (%) | 发芽势 Germination energy (%) | 发芽指数 Germination index | 平均发芽速率 Mean germination rate/d?1 |
| 对照 Control | 67.29±1.42b | 49.49±0.07bc | 1.88±0.04c | 9.38±1.03a |
| SS-1-14 | 94.44±5.56a | 73.80±0.05a | 3.73±0.10a | 11.77±0.37a |
| SS-2-3 | 83.49±8.94ab | 39.93±0.03c | 3.10±0.26b | 9.68±0.55a |
| SS-2-22 | 90.81±2.93a | 67.27±0.07ab | 3.66±0.07a | 10.92±0.98a |
图2
3株种子际真菌的26种植物激素的产生情况 A. 对照组总离子色谱图Total ion chromatograms of control; B. SS-1-14总离子色谱图Total ion chromatograms of SS-1-14; C. SS-2-3总离子色谱图Total ion chromatograms of SS-2-3; D. SS-2-22总离子色谱图Total ion chromatograms of SS-2-22; E. 产生激素种类与含量Types and contents of producing hormones. IAA: 吲哚乙酸Indoleacetic acid; IBA: 吲哚丁酸Indolebutyric acid; IAA-ASP: 吲哚乙酸-天冬氨酸Indoleacetic acid-aspartic acid; IAA-Glu: 吲哚乙酸-谷氨酸Indoleacetic acid-glutamic acid; IAN: 吲哚-3-乙腈Indole-3-acetonitrile; IPYA: 吲哚-3-丙酮酸Indole-3-pyruvic acid; IAM: 吲哚-3-乙酰胺Indole-3-acetamide; TAM: 3-(2-氨乙基) 吲哚Tryptamine; ABA: 脱落酸Abscisic acid; JA: 茉莉酸Jasmonic acid; MEJA: 茉莉酸甲酯Methyl jasmonate; JA-ILE: 茉莉酸-异亮氨酸Jasmonic acid-isoleucine; OPDA: 12-氧代-植物二烯酸12-oxo phytodienoic acid; SA: 水杨酸Salicylic acid; MESA: 水杨酸甲酯Methyl salicylate; SAG: 水杨酸葡萄糖苷Salicylic acid glucoside; TZR: 反玉米素核苷Trans-Zeatin-riboside; DZR: 二氢玉米素核糖Dihidrozeatin riboside; Zeatin玉米素; TZeatin: 反-玉米素Trans-Zeatin; IP: 异戊烯基腺嘌呤Isopentenyladenine; IPR: N6-异戊烯基腺苷N6-isopentenyladenosine; GA1: 赤霉素A1 Gibberellin acid 1; GA3: 赤霉素A3 Gibberellin acid 3; GA4: 赤霉素A4 Gibberellin acid 4; GA7: 赤霉素A7 Gibberellin acid 7."
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